219/2016 Coll.
GOVERNMENT REGULATION


Dated July 7, 2016

Conformity assessment of pressure equipment when made available on the market

Government directs pursuant to § 4 and § 50 par. 5 of Law no. 90/2016 Coll., On
conformity assessment of products when made available on the market (hereinafter
"Act") || |
§ 1
Subject Matter


(1) This regulation implements the relevant regulations of the European Union ^ 1) and
regulates technical requirements for pressure equipment, which must meet
to the market, conditions and procedures for making available on the market and
methods of conformity assessment.

(2) This regulation applies to the design, manufacture and conformity assessment
pressure equipment and assemblies with a maximum allowable pressure PS greater than 0.5 bar
.

(3) This regulation does not apply to

A) pipelines comprising piping or conduit system,
designed to carry liquids or substances into or out of the pressure device
located on land or at sea;
remote part of the pipe lines are extreme, locking devices located in the circuit pressure
devices all attached devices designed specifically for the pipeline
management; exemption under this subparagraph shall not apply to standard
pressure equipment which may be found in pressure reduction or
compressor stations,

B) networks for the supply, distribution and discharge of water and associated equipment and supply
channels such as penstocks, pressure tunnels,
pressure shafts for hydroelectric installations and their related specific accessories
,

C) simple pressure vessels ^ 2)

D) aerosol dispensers ^ 3)

E) equipment designed to operate vehicles under other laws; 4)
or the directly applicable European Union ^ 5)
governing the approval of vehicles

F) equipment, which according to § 4 of classified higher than category I and belongs
between the products under other laws ^ 6)

G) equipment intended for use as weapons, ammunition or war
material

H) equipment specially designed for use in nuclear power plants, whose
failure can cause leakage of radioactivity

I) well-control equipment used in the exploration and extraction industry
oil, gas or geothermal sources in underground storage
which are designed to maintain or control well pressure;
control devices for drilling equipment are particularly wellhead, which is the eruption cross
protierupční equipment, manifolds and all equipment that
UPSTREAM,

J) equipment comprising casings or machinery where the dimensioning, choice
material and manufacturing rules are based primarily on requirements for sufficient
strength, rigidity and stability to meet the static and dynamic
operational effects or other operational characteristics and not
pressure is a significant design factor; these devices are particularly

First engines including turbines and internal combustion engines, or

Second steam engines, gas or steam turbines, turbo-generators,
compressors, pumps and actuating devices

K) blast furnace, including the cooling system, hot wind
dust collectors and cleaners of blast furnace gas, blast furnace direct
reduction, including the furnace cooling, gas converters and pans for melting
, de-gassing and casting of steel, iron and non-ferrous metals
,

L) Enclosures for high voltage electrical equipment such as switchgear
equipment, control gear, transformers, and rotating machines,

M) pressure pipes for the containment of transmission systems, for example
electrical power and telephone cables,

N) ships, rockets, aircraft and mobile offshore installations, as well as equipment
specifically intended for installation on board or the propulsion,

O) pressure equipment consisting of a flexible casing, these devices are particularly
tires, air cushions, balls, inflatable boats and other
similar pressure equipment,

P) exhaust and inlet silencers,

Q) bottles or cans for carbonated drinks, intended to
final consumption

R) containers designed for the transport and distribution of drinks having a PS. In
not more than 500 bar. L and the maximum allowable pressure not exceeding 7 bar
,

S) devices, which are covered by other legislation ^ 7), and devices
covered by the regulations of the International Maritime Organization
transport of dangerous goods by sea,

T) radiators and pipes in warm water heating systems and

U) vessels designed to contain liquids with a gas pressure above the liquid
not more than 0.5 bar.

§ 2


Definitions
For the purposes of this Regulation

A) pressure equipment means vessels, piping, safety accessories and pressure
equipment, including elements attached to pressurized parts,

Such as flanges, nozzles, couplings, supports, lifting lugs,

B) container housing designed and built so that it can be filled
fluid under pressure, including parts that are not directly
attachments up to the point of connection to other devices;
vessel may consist of more than one chamber,

C) conduit piping components intended for the transport of fluids, when
connected together to form a pressure system;
pipeline includes in particular a pipe or system of pipes or tubes, fittings, expansion
joints, hoses, or possibly other pressure; for pipe
construed Heat exchangers consisting of pipes for the cooling or heating air
,

D) safety gear devices designed to protect pressure equipment
against exceeding the allowable limits, including
devices for direct pressure limitation, such as safety valves, bursting disc safety
devices, buckling rods, controlled safety systems and
limiting devices, which either activate the means for correction or
provide for shutdown or shutdown and lockout, such as pressure
switches, temperature switches or fluid level switches and measuring, controlling and regulating devices
safety-related

E) pressure accessory device with an operational function and
body is subjected to pressure,

F) pressure such pressure, which is related to atmospheric pressure, in
result of which the vacuum is a negative value,

G) maximum allowable pressure specified by the manufacturer the maximum pressure for which
pressure equipment is designed and defined it in a certain place of priority
, connection of protective or limiting devices or the top spot
pressure equipment, or in any other
given site, the maximum allowable pressure is designated by
PS

H) the highest or the lowest allowable temperature specified by the manufacturer
highest or the lowest temperature for which the pressure equipment is designed
, the highest and lowest allowable temperature is called
letters TS

I) the volume of the internal volume of a chamber, including the volume
nozzles to the first connection or weld and excluding the volume of permanent
internal components, while the volume is denoted by the letter V

J) the nominal size numerical designation of size which is common to all
part of a piping system indicated by outside diameters or by thread size
, with the reference of the reasons is rounded
number that only loosely related to manufacturing dimensions;
nominal size is designated by DN followed by a number,

K) liquid gases, liquids and vapors in pure phase as well as mixtures
, the fluid may contain a suspension of solids,

L) Permanent joints joints which can not be disconnected except
destructive manner

M) European approval for materials, technical document, which are defined
characteristics of materials intended for repeated use in the manufacture
pressure equipment not covered by any harmonized
norm

N) producer is also a person who manufactures pressure equipment or assembly or
keeps pressure equipment or assembly designed or manufactured and
the pressure equipment or assembly uses for its own account

O) technical specification document that prescribes technical requirements
which has a pressure device or assembly to meet.

§ 3

Technical requirements for pressure equipment

(1) The technical requirements for pressure equipment are essential
safety requirements set out in Annex no. 1 hereto,
whose fulfillment is demonstrated conformity assessment.

(2) Technical requirements must be met for

A) vessels, except vessels referred to in point b), intended for

First gases, liquefied gases, gases dissolved under pressure, vapors and also
those liquids whose vapor pressure at the maximum allowable temperature is greater than 0.5
bar higher than normal atmospheric pressure of 1013 mbar, in these | || limits:

1.1 for fluids in Group 1 with a volume greater than 1 L and a product of PS. In
greater than 25 bar. L or pressure PS greater than 200 bar according to Figure 1
Annex no. 2 to this Order or

1.2 for fluids in Group 2 with a volume greater than 1 L and a product of PS. In
greater than 50 bar. L or pressure PS greater than 1 000 bar, and all
portable extinguishers and bottles for breathing apparatus according to the chart 2
Annex no. 2 hereto and

Second liquids whose vapor pressure at the maximum allowable temperature
does not exceed the normal atmospheric pressure of 1013 mbar by more than 0,5 bar
following limits:

2.1 for fluids in Group 1 with a volume greater than 1 L and a product of PS. In
greater than 200 bar. L or pressure PS greater than 500 bar according to Figure 3
Annex no. 2 to this Order or


2.2 for fluids in Group 2 with a pressure PS greater than 10 bar and a product of PS
. In more than 10 000 bar. L or pressure PS greater than 1000 bar by
graph 4 of Annex no. 2 to this Order,

B) pressure equipment exposed to flames or otherwise
heated with the danger of overheating intended for generation of steam or hot
water at temperatures higher than 110 ° C, the volume of which is greater than 2 L, and
all pressure cookers according to the graph 5 of Annex no. 2 to this Order,

C) pipes intended for

First gases, liquefied gases, gases dissolved under pressure, vapors and liquids
whose vapor pressure at the maximum allowable temperature is greater than
0.5 bar higher than normal atmospheric pressure of 1013 mbar, these limits
:

1.1 for fluids in Group 1 with a DN greater than 25 (graph 6 of Annex no. 2
hereto) or

1.2 for fluids in Group 2 with a DN greater than 32 and a product of PS.
DN greater than 1000 bar according to the graph 7 of Annex no. 2 hereto and

Second liquids whose vapor pressure at the maximum allowable temperature
does not exceed the normal atmospheric pressure of 1013 mbar by more than 0,5 bar
following limits:

2.1 for fluids in Group 1 with a DN greater than 25 and a product of PS.
DN greater than 2000 bar graph by 8 Annex no. 2 to this Order or

2.2 for fluids in Group 2 with a PS greater than 10 bar, a DN greater than 200 and a product of PS
. DN greater than 5000 bar graph by 9 Annex no. 2 to this Order and


D) the safety and pressure kits intended for pressure equipment
covered by letters a), b) or c), including pressure equipment
incorporated into an assembly.

(3) Technical requirements must also be met with reports that contain at least one
pressure equipment covered by paragraph 2, when it comes to


A) the assemblies intended for generating steam or superheated water at a temperature higher than
110 ° C comprising at least one pressure equipment exposed
of fired or otherwise heated, wherein there is a danger of overheating
or

B) Assemblies other than those listed in subparagraph a), if a manufacturer
intended for supply to the market and put into service as assemblies.

(4) Notwithstanding paragraph 3 point. ) must assemblies intended for generating
hot water at temperatures exceeding 110 ° C, to which is attached manually
solid fuel and a PS. V is greater than 50 bar L,
meet the essential safety requirements set out in paragraphs 2.10, 2.11 and 3.4
and in point 5. a) and d) of the Annex no. 1 hereto.

(5) Pressure equipment and assemblies below or equal to the limits
values ​​set out in paragraph 2. a), b) or c) and paragraph 3
must be designed and manufactured in accordance with good engineering practice
used in any of the EU Member States in order to
ensure their safe use. These
Pressure equipment and assemblies must be accompanied by instructions for use. Without prejudice to Regulation
government and harmonizing European Union legislation governing
placing CE marking, these devices and assemblies are affixed CE marking
.

§ 4
Classification of pressure equipment


(1) Pressure equipment referred to in § 3 para. 2 are classified into categories
in accordance with Annex no. 2 to this Regulation depending on
danger. For the purposes of such classification fluids shall be divided for

A) group 1, which includes substances and mixtures contained in pressure
devices with the highest allowable temperature which exceeds the flash point
fluid; This group consists of substances and mixtures, whose definitions are set out in Article
. 2 points 7 and 8 of Regulation (EC) no. 1272/2008, which are
classified as dangerous according to the following classes of physical hazards
or health hazards set out in parts 2 and 3
Annex I to Regulation (EC) no. 1272/2008:

First unstable explosives or explosives of Division 1.1, 1.2, 1.3, 1.4 and 1.5
,

Second flammable gases category 1 and 2

Third oxidising gases Category 1

Fourth flammable liquids categories 1 and 2

Fifth flammable liquids Category 3, where the maximum allowable temperature higher
flashpoint

6th flammable solids category 1 and 2

7th self-reactive substances and mixtures types A through F,

8th pyrophoric liquids category 1

9th pyrophoric solids category 1

10th substances and mixtures which in contact with water, emit flammable gases
category 1, 2 and 3,

11th oxidising liquids categories 1, 2 and 3,

12th oxidising solids Category 1, 2 and 3,

13th Organic peroxides types A to F

14th Acute oral toxicity category 1 and 2

15th The acute dermal toxicity category 1 and 2

16th Acute inhalation toxicity category 1, 2 and 3

17th toxicity for specific target organs - single exposure category 1
and


B) Group 2, consisting of substances and mixtures, not mentioned in a letter
).

(2) If a vessel is composed of several chambers, it
classified in the highest category applicable to the individual pressure
spaces. If it contains a chamber several fluids, classification shall
basis of the fluid which requires the highest category.

§ 5

Available on the market and putting into service

(1) Pressure equipment and assemblies can be supplied to the market and under the conditions specified by the manufacturer
put into operation only if
meet the requirements of this Regulation and
properly installed, maintained and used for intended purpose.

(2) At trade fairs, exhibitions and similar events or demonstrations can show
pressure equipment or assemblies, which are not
compliance with this regulation, if a visible sign clear that this
pressure equipment or assemblies are not in compliance and may not be delivered on
market or put into service until brought into conformity. When
demonstrations must be taken security measures to ensure the safety of people
.

§ 6
Producer


(1) When placing pressure equipment or assemblies on the market or use for their own
need to ensure that the manufacturer

A) for pressure equipment or assemblies as defined in § 3 para. 2 and 3 to
these devices or assemblies have been designed and manufactured in accordance with the technical requirements
and

B) for pressure equipment or assemblies as defined in § 3 para. 5, so this
equipment or assemblies have been designed and manufactured in accordance with good engineering practice
.

(2) In the case of pressure equipment or assemblies as defined in § 3 para. 2 and 3
manufacturer shall establish the technical documentation as set out in Annex no. 3
hereto and perform or have performed the conformity assessment procedure || | specified in § 11. If the compliance of the pressure equipment or assemblies
with the relevant requirements of the appropriate conformity assessment procedure
proved, manufacturers draw up an EU declaration of conformity and placed on the pressure equipment or assembly
CE marking.

(3) Manufacturer keeps technical documentation and the EU declaration of conformity
period of 10 years from the commissioning of pressure equipment or assemblies on the market.

(4) The manufacturer shall ensure that for pressure equipment or assemblies
bear a type or batch or serial number or other
element allowing their identification, or in cases where the size or nature
equipment or assemblies prevents them from being required
information provided on the packaging or in a document accompanying the device.

(5) The manufacturer shall provide to the pressure equipment or assembly, or, if this is not
possible on the packaging or in a document accompanying the device or assembly of its
name or trade name or trademark and address
for delivery at which he can be contacted. Mailing Address must be
address of the place at which the manufacturer can actually be reached.
Contact details are given in a language easily understood by end users and
supervisory authority.

(6) The manufacturer shall ensure that the pressure equipment or assembly that
are set out in § 3 para. 2 and 3, accompanied by clear and understandable
instructions and safety information in accordance with sections 3.3 and 3.4 of Annex .
1 of this regulation, and pressure equipment or assemblies, which are set out in § 3
. 5 is accompanied by clear and understandable instructions and safety information
under § 3 para. 5. Operating and information in points 3.3 and 3.4
Annex no. 1 hereto shall be given in Czech language.

(7) Manufacturer performed to protect the health and safety of final users
sample testing of pressure equipment or assemblies supplied to the market
necessary investigations and, if necessary, given the risks that pressure equipment
or assemblies represent. These tests and investigations are carried out in
extent needed to confirm or refute existing risks posed
pressure equipment or assembly due to the manufacturer
its intended use. The producer keeps records of complaints, non-conforming
pressure equipment or assemblies and withdraw such equipment or assemblies
from circulation, and these activities inform distributors.

§ 7
Authorised representative


Authorized representative shall keep the EU declaration of conformity and the technical documentation needs
supervisory authority for 10 years since the
pressure equipment or assemblies on the market.

§ 8
Importer


(1) The importer before placing pressure equipment or assemblies provided for in § 3
. 2 and 3 on the market, ensure that the manufacturer performed the assessment
Conformity in accordance with § 11, that the manufacturer has drawn up the technical documentation,
to pressure equipment or assemblies bear the CE marking to them
was accompanied by instructions and safety information in accordance with paragraphs 3.3 and 3.4

Annex no. 1 hereto and that the manufacturer has complied with the requirements set
in § 6 para. 4 and 5.

(2) The importer before placing pressure equipment or assemblies provided in
§ 3. 5 on the market shall ensure that the manufacturer has drawn up the technical documentation
that the pressure equipment or assembly accompanied by instructions for use
and that the manufacturer has complied with the requirements set out in § 6 para. 4 and 5.

(3) The importer shall indicate on the pressure equipment or assembly, or, if this is not
possible on the packaging or in a document accompanying the device or assembly of its
name or trade name or trademark and address
delivery, on which he can be contacted. Contact details are given in
language easily understood by end users, and other users
supervisory authority.

(4) The importer shall ensure that the pressure equipment or assemblies
set out in § 3 para. 2 and 3, accompanied by instructions and safety information in
accordance with paragraphs 3.3 and 3.4 of Annex no. 1 hereto
in the Czech language and to pressure equipment or assemblies referred to in § 3 para. 5
accompanied by instructions and safety information in the Czech language.

(5) The importer performed to protect the health and safety of final users
sample testing of pressure equipment or assemblies supplied to the market
necessary investigations and, if necessary, given the risks that pressure equipment
or assemblies represent. These tests and investigations are carried out in
extent needed to confirm or refute existing risks posed
pressure equipment or assembly due to the manufacturer
its intended use. The importer shall keep records of complaints, non-conforming
pressure equipment or assemblies and withdraw such equipment or assemblies
from circulation, and keep informed about these activities
distributors.

(6) The importer for 10 years after the equipment or assembly
market keep a copy of the EU declaration of conformity
supervisory authority and ensure that the supervisory authority may, upon request technical
documentation.

§ 9
Distributor


(1) Distributor prior to delivery of the equipment or assembly
set out in § 3 para. 2 and 3 on the market verifies whether

A) of pressure equipment or assembly carries the CE mark

B) the pressure equipment or assembly, accompanied by the required documents and
instructions and safety information in accordance with paragraphs 3.3 and 3.4 of Annex no.
1 hereto in the Czech language and

C) the manufacturer and the importer have complied with the requirements set out in § 6 par. 4 and 5 and § 8 paragraph
.
Third
(2) Distributor prior to delivery of the equipment or assembly shown in
§ 3. 5 on the market verifies whether

A) the pressure equipment or assembly attached manual in Czech language and


B) the manufacturer and the importer have complied with the requirements set out in § 6 par. 4 and 5 and § 8 paragraph
.
Third
§ 10

Time identification of the operator

Operators for a period of 10 years from the delivery of the equipment or assembly
market holds data that can be used at the request of the supervisory authority
identify the operator who had
pressure equipment or assembly or to whom the pressure equipment or assembly, he added.

§ 11

Conformity assessment procedures

(1) The conformity assessment procedures for pressure equipment are set out in Annex
no. 3 hereto. These procedures are set out in
depending on the category to which the equipment is classified in accordance with
§ 4. For each category, the following procedures:

A) Category I

Internal production control (module A) set out in Part 1 of Annex no. 3 to
this Regulation

B) Category II

First Internal production control with monitoring of pressure equipment under the supervision of
random intervals Module (A2) set out in Part 2 of Annex.
3 to this Order,

Second quality assurance of the production process (module D1)
set out in Part 6 of Annex no. 3 to this Order, or

Third quality assurance of final inspection and testing of pressure equipment
(module E1) set out in Part 8 of Annex no. 3 to this Order,

C) Category III

First EU-type examination (Module B) - EU examination of production type
set out in Part 3 of Section 3.1 of Annex no. 3 hereto and simultaneously
one of the following:

1.1 Conformity to type based on quality assurance of pressure equipment
(Module E) referred to in section 7 of Annex no. 3 to this Order, or

1.2 Conformity to type based on internal production control with controls
pressure equipment under supervision at random intervals (Module C2
) set out in Part 4 of Annex no. 3 to this Order,

Second EU-type examination (Module B) - EU design type examination
set out in Part 3 of Section 3.2 of Annex no. 3 hereto and simultaneously
one of the following:

2.1 Conformity to type based on quality assurance of the production process

(Module D) referred to in section 5 of Annex no. 3 to this Order, or

2.2 Conformity to type based on the verification of the pressure device (module F)
set out in section 9 of Annex no. 3 to this Order, or

Third Conformity based on full quality assurance (module H)
set out in section 11 of Annex no. 3 to this Order,

D) Category IV

First EU-type examination (Module B) - EU examination of production type
set out in Part 3 of Section 3.1 of Annex no. 3 hereto and simultaneously
one of the following:

1.1 Conformity to type based on quality assurance of the production process
(Module D) referred to in section 5 of Annex no. 3 to this Order, or

1.2 Conformity to type based on the verification of the pressure device (module F)
set out in section 9 of Annex no. 3 to this Order,

Second Conformity based on unit verification (module G)
set out in Part 10 of Annex no. 3 to this Order, or

Third Conformity based on full quality assurance with design examination
(module H1) set out in Part 12 of Annex no. 3 to this Order.

(2) A manufacturer may choose any of the procedures laid down for the category to which
pressure equipment is situated. The manufacturer may also use
any of the procedures which apply to a higher category.

(3) As part of quality assurance procedures for pressure equipment
categories III and IV set out in § 3 para. 2 point. a) 1, § 3 para. 2
point. a) Section 2.1 and § 3 para. 2 point. b) the notified body during
unannounced visits to the manufacturer takes in production or storage areas
sample of establishments to perform, or have performed
final assessment in paragraph 3.2 of Annex no. 1 hereto.
For this purpose, the manufacturer notified body of the intended schedule
production. During the first year of production the notified body shall take place at least 2
visits to the manufacturer. The frequency of subsequent visits to the manufacturer specifies
notified body on the basis of the criteria set out in paragraph 4.4 of modules D, E and H and
paragraph 5.4 Module H1 Annex no. 3 to this Order.

(4) In the case of production of vessels and pressure equipment of category III
set out in § 3 para. 2 point. b) the notified body in the context of
Module H perform or have performed the final assessment in accordance with paragraph 3.2
Annex no. 1 hereto for each unit.
To this end, the manufacturer notified body of the intended schedule of production.

(5) Reports under § 3 para. 3 are subjected to a global conformity assessment
which includes this assessment:

A) assessment of each item of pressure equipment referred to in § 3 para. 2, of which
assembly is formed and which had not been subjected to conformity assessment procedures
a separate CE marking; assessment procedure is given
categories each device

B) assessment of the integration of the various components of the assembly by
sections 2.3, 2.8 and 2.9 of Annex no. 1 hereto;
this assessment is carried out in terms of the highest category applicable to the issue
equipment, disregarding the safety gear, or

C) assessment of the protection of an assembly against exceeding the permissible operating limits
according to sections 2.10 and 3.2.3 of Annex no. 1 hereto;
this assessment is carried out in terms of the highest category applicable to the
pressure equipment to be protected.

(6) Documents relating to the conformity assessment procedures shall be drawn up in
official language or languages ​​of the Member State of the European Union, which is
notified body carrying out the conformity assessment procedures is established or in
language, which the manufacturer with the notified body agrees.

§ 12

European approval for materials

(1) European approval for materials issued one of the notified bodies
specially designed for this task, based on the request of one or more manufacturers of materials or
pressure equipment. The notified body shall determine and
shall carry out appropriate inspections and tests of the types of material
to certify their compliance with the corresponding requirements of this Regulation
. In the case of materials for which safe use has been recognized
before 29 November 1999, the notified body when certifying compliance
account of the existing data.

(2) Before issuing European approval for materials, the notified body
inform the Member States and the European Commission so that they will send
documents proving the fulfillment of the obligations under paragraph 1. Within 3 months from sending these documents
a Member state of the European Union or the European Commission may
to comment, stating the reasons for its position.
Notified body shall issue the European approval for materials taking into account
comments submitted.

(3) A copy of the European approval for materials should be addressed to the Member States of the European Union
, notified bodies and the European Commission, which

Publish and update references to those approvals in the Official Journal of the European Union
.

(4) If the notified body which issued the European approval for materials
finds that should not be released, or if the given type
materials is covered by a harmonized standard proceed according to § 24 para. 4 || | Law and European approval for materials withdrawn. Of any withdrawal
shall immediately inform the other Member States of the European Union
notified bodies and the European Commission.

§ 13
Presumption of conformity


(1) If the pressure equipment or an assembly provided for in § 3 para. 2 and 3
in conformity with harmonized standards or parts thereof, which were
published in the Official Journal of the European Union, it is considered that is
complies with the essential technical requirements to which such standards
or parts thereof apply.

(2) Where the materials used for the manufacture of pressure equipment or assemblies
conforming with European approvals for materials, which were
published in the Official Journal of the European Union in accordance with § 12 paragraph
. 3, it is understood that they are in conformity with the relevant essential
technical requirements.

§ 14

EU declaration of conformity

(1) The EU declaration of conformity shall demonstrate compliance with the technical requirements
set out in Annex no. 1 hereto.

(2) the EU declaration of conformity is drawn up according to the model set out in Annex
no. 4 hereto. Statement contain the information specified in
modules set out in Annex no. 3 to this Order and shall be continuously updated
. The EU declaration of conformity will also translate into the language or languages ​​required
EU Member State in which the pressure equipment or assembly
states or supplies on the market.

(3) Where the pressure equipment or assembly is subject to more
harmonization of European Union legislation, providing for the development of
EU declaration of conformity, produced a single EU declaration of conformity with
links to all these regulations, according to which the conformity assessment
including the publication references. The single EU declaration of conformity
may take the form of a folder consisting of declarations of conformity issued for each
regulations.

§ 15

CE and other markings

(1) The CE marking, which is placed before the
pressure equipment or assemblies on the market, is placed visibly, legibly and indelibly

A) for all pressure equipment under § 3 para. 2, or its production
label, or

B) for each report under § 3 para. 3, or a product label.

(2) If the placement referred to in paragraph 1 because of the nature
pressure equipment or assembly is not possible or justified, the CE marking must
on the packaging and accompanying documents.

(3) pressure equipment or assemblies referred to in paragraph 1 shall be full
or in a state that allows final assessment as set out in paragraph 3.2
Annex no. 1 hereto.

(4) The CE marking may not be affixed to each individual pressure
devices that make up the assembly. Individual items of pressure equipment already
bearing the CE marking when incorporated into his report, to bear this designation
continue.

(5) identification number of the notified body, which participated
conformity assessment pursuant to sections 2 and 4 to 12 of Annex no. 3 to this
regulation, coupled to the CE marking notified body, or by his
instructions of the manufacturer or his authorized representative.

(6) The CE marking and, where applicable, the identification number referred to in paragraph 5
can follow any other mark indicating a special risk or use
.

§ 16
Formal shortcomings


The formal deficiency is considered when

A) the CE marking has been placed in conflict with Art. 30 of the European
Parliament and Council Regulation (EC) no. 765/2008 of 9 July 2008
the requirements for accreditation and supervision market
relating to the marketing of products on the market and repealing Regulation (EEC) no. 339/93 or §
15

B) the CE marking has not been placed,

C) identification number of the notified body was placed in conflict with §
15 or has not been placed,

D) designation and label data specified in paragraph 3.3 of Annex no. 1 to
this Regulation have not been located or have been placed in conflict with § 15
or paragraph 3.3 of Annex no. 1 hereto, || |
E) the EU declaration of conformity has not been drawn,

F) the EU declaration of conformity has not been drawn up in accordance with this Regulation
,

G) the technical documentation is missing or incomplete,

H) the information specified in § 6 para. 5 or § 8. 3
missing or incorrect or incomplete, or

I) has not fulfilled other administrative requirement in § 6 or § 8
or administrative requirement in § 6 para. 1, 5, 6 or
in § 8. 1, 3, 6, or 7 of the Act.

§ 17
Transitional provisions



(1) Pressure equipment and assemblies may continue to be placed into operation
if they comply with the legislation in force before 29 May 2002
and prior to that date on the market.

(2) Pressure equipment and assemblies meeting the requirements of Government Regulation no.
26/2003 Coll., Laying down technical requirements for pressure equipment,
amended, may continue to be available on the market or | || put into operation if placed on the market before 1 July 2015.

(3) Valid certificates and other documents certifying found
actually issued by NBs based on Government Regulation no. 26/2003 Coll
. They remain in force and shall be deemed
certificates and other documents certifying the facts established under this Regulation.

§ 18
Repealing provisions


Repealed:

First Government Regulation no. 26/2003 Coll., Laying down technical requirements for pressure equipment
.

Second Government Regulation no. 621/2004 Coll., Amending Government Regulation no.
26/2003 Coll., Laying down technical requirements for pressure equipment.

Third Government Regulation no. 93/2015 Coll., Amending Government Regulation no.
26/2003 Coll., Laying down technical requirements for pressure equipment, as amended
Government Decree no. 621/2004 Coll.

§ 19
Efficiency


This regulation comes into force on 19 July 2016.
Prime Minister
:

Mgr. Sobotka

Minister of Industry and Trade:

Ing. Mládek, CSc.


Příl.1
Essential safety requirements
PRELIMINARY PROVISIONS


First Basic safety requirements of this Regulation shall apply to certain
pressure equipment only when the relevant
danger occurs when using pressure equipment under conditions that
manufacturer may reasonably anticipate.

Essential safety requirements for pressure equipment laid down in this Annex
also apply to assemblies, if there is among them a similar
risk.

Second Manufacturer analyze the hazards and risks in order to identify those which the
due to pressure his equipment account;
facility designs and manufactures with respect to this analysis.

Third Basic safety requirements are interpreted and applied
manner that takes into account the state of the art and the usual practice at the time
design and production facilities as well as technical and economic aspects,
which correspond to the high level of health and safety.

First GENERAL REQUIREMENTS

1.1 Pressure equipment must be designed, manufactured and checked,
if applicable equipped and installed, in such a way as to
after its commissioning in accordance with the manufacturer's instructions or under reasonably foreseeable conditions
ensure its safety .

1.2 When choosing the most appropriate solutions, the manufacturer must apply the following principles
in this order:

A) far as reasonably achievable eliminate or reduce hazards,

B) apply appropriate protection measures against hazards that can not be
excluded or

C) inform users about any residual dangers and
is necessary to take measures to reduce the risks during installation or use
.

1.3 Where the potential for misuse is known or can be clearly
predict, pressure equipment must be designed to prevent
risks that this improper use of gas, or if that is not possible
the user must be used in that way before the pressure
equipment, adequate warning.

Second DRAFT
2.1 General


Pressure equipment must be properly designed taking all relevant factors into
to ensure the safety of equipment
throughout its intended life.

The pressure equipment design must incorporate appropriate safety coefficients
using comprehensive methods which are known to be suitable
account of an adequate safety margins against all kinds
disturbances that come into consideration.

2.2 Design for adequate strength

2.2.1 Pressure equipment must be designed for loadings appropriate
its intended use and other reasonably foreseeable operating conditions
. In particular it must take into account the following factors:

A) internal and external pressure,

B) the ambient and working temperature

C) static pressure and mass of contents in operating and test conditions,

D) traffic, wind, earthquake,

E) reaction forces and moments which result mainly supports, attachments and
pipeline

F) corrosion, erosion and fatigue and

G) decomposition of unstable fluids.

It is necessary to take into account different load, which can act simultaneously with
account the probability of their simultaneous occurrence.

2.2.2 Design for adequate strength must be based on one of these methods
:


A) the calculation method set out in Section 2.2.3, if necessary
complemented by experimental design technique specified in paragraph 2.2.4, or


B) designing an experimental method without calculation
specified in paragraph 2.2.4, if the product of PS. V is less than 6000 bar. L or when a PS
. DN less than 3 000 bar.
2.2.3 Calculation method


A) Pressure containment and other loading aspects

Allowable stresses for pressure equipment must be limited with regard to
failure modes under operating conditions, it is possible to reasonably predict
. Therefore, it is necessary to use safety factors that
eliminate fully any uncertainty arising out of manufacture,
actual operational conditions, stresses, calculation models, as well as
material behavior.

These calculation methods must provide sufficient safety
appropriate in appropriate cases the requirements set out in item 7

The above requirements can be met by applying one of the following methods
as appropriate, or as a supplement to other methods or in combination with her


1) a proposal based on patterns,

2) design by analysis, or

3) design by fracture mechanics.

B) Strength

To ensure the strength of the pressure equipment must be used
Appropriate design calculations, especially

1) The calculation pressure must not be less than the maximum allowable pressure and
must take into account static head and dynamic fluid pressures and the decomposition of unstable fluids
. If the vessel is separated into individual pressure chambers
must partition wall designed with
highest possible pressure in a particular chamber pressure relative to the lowest pressure possible in
adjoining chamber,

2) The calculation temperatures must allow for appropriate safety margins,

3) the design must take appropriate account of all possible combinations
temperature and pressure which might arise under reasonably foreseeable operating conditions
device

4) The maximum stresses and peak stress concentrations must be kept within safe limits
,

5) the calculation for pressure containment must utilize the values ​​appropriate to the properties
material, based on documented data, with
regard to the provisions set out in Section 4 together with appropriate safety factors
. Material characteristics, which is
where appropriate, be taken into account include

6) yield strength or proof stress at 0,2%, respectively. 1.0%, while
calculation temperature,

7) tensile

8) time-dependent strength, i.e., creep strength,

9) Fatigue value

10) Young's modulus (modulus of elasticity)

11) The appropriate amount of plastic deformation,

12) value ductility

13) fracture toughness,

14) in the case of welded joints must be applied to the material properties suitable
joint coefficient, on the type of
non-destructive testing, the materials joined and the operating conditions envisaged
,

15) The design must take appropriate account of all reasonably foreseeable degradation mechanisms
such as corrosion, creep and fatigue
, the intended use of the device. The instructions referred to in 3.4
attention is drawn to specific aspects of the design which are relevant to the life
devices such as

I) creep: design hours of operation at specified
temperature

Ii) in the case of fatigue: design number of cycles at specified stress and


Iii) in the case of corrosion: design corrosion allowance.

C) Stability aspects

However, where the calculated thickness to ensure sufficient stability
structure, it is necessary to take the necessary corrective measures to
account the risks associated with transportation and handling.

2.2.4 Experimental design method

The design of the device as a whole or its parts can be verified
appropriate test program carried out on a representative sample
device or category of devices.

Test program must be prior to testing
clearly defined and approved by the notified body responsible for conformity assessment module
proposal, if one exists.

The program must define test conditions and criteria for acceptance or rejection
. Before testing must be measured actual values ​​
essential dimensions and characteristics of the materials from which the equipment under test consists
.

Where applicable, it must be possible to observe during tests
critical zones of the pressure equipment with adequate instrumentation capable
record with sufficient precision strain and stress.

Test program must include

A) pressure test, the purpose of which is to check whether the pressure

Defined safety margin in relation to the maximum allowable pressure
equipment does not exhibit significant leaks or deformation
exceed the set limit.

Test pressure must be determined based on the differences between the values ​​of
geometrical and material characteristics measures under test
conditions and the values ​​used for design purposes; it must take into account
differences between the test and design temperatures.

B) where the risk of creep or fatigue, the appropriate tests
based on operating conditions prescribed for the device, such as a
time at specified temperatures, number of cycles at specified stress levels
and

C) where necessary, additional tests concerning other factors set out in paragraph 2.2.1
., Such as corrosion or external damage.

2.3 Provisions to ensure safe handling and operation

Prescribed method for operating pressure equipment shall exclude any
reasonably foreseeable risk in operation. Where it falls
account, special attention must be paid to:

A) closures and openings,

B) dangerous discharge of pressure relief blow,

C) devices to prevent physical access to the device
pressure or vacuum

D) surface temperature with respect to the intended use and

E) decomposition of unstable fluids.

Particular, pressure equipment fitted with an access door must be equipped
automatic or manual device enabling the user
easily to ascertain that the opening can be opened without risk. In the case
slam-pressure equipment must be additionally fitted with a device which prevents its opening
if the pressure or temperature of the fluid presents
risk.

2.4 Means of control

A) Pressure equipment must be designed and constructed so that it is possible
carry out all the necessary checks to ensure safety.

B) Where it is necessary to ensure the continued safety devices
must be provided to allow it to determine the internal state of
devices, such as access openings allowing physical access to the inside of the pressure device
order to carry out appropriate checks
safely and ergonomically.

C) Other means of ensuring the safe condition of the pressure
device can be used in these situations:

I) if the pressure is too small for physical access to its
interior

Ii) where opening the pressure equipment would adversely affect its
inside, or

Iii) if it is proven that contained a substance not to be harmful to the material
from which the pressure equipment is made and can not reasonably predict
no other internal degradation mechanisms.

2.5 Drainage and venting

Where necessary, they must be provided with adequate resources to enable
draining and venting of pressure equipment:

A) to avoid adverse effects such as water hammer, vacuum collapse
impact, corrosion and uncontrolled chemical reactions. It is necessary to take into account
All stages of operation and testing, particularly pressure testing and

B) make it possible safely to carry cleaning, inspection and maintenance
.

2.6 Corrosion or other chemical

Where necessary, it must be ensured allowance or protection against
corrosion or other chemical attack, taking due account of the intended and reasonably foreseeable use
.

Wear 2.7

If there may be considerable erosion or abrasion, measures must be taken, that


) Reduce these effects to a minimum by appropriate design,
example, increasing the thickness of the material or using lining or
lap,

B) allow the replacement of parts which are most affected and

C) the instructions set out in Section 3.4 highlights
measures necessary to ensure the continued safe use.

Reports 2.8

Assemblies must be designed so that:

A) assembled structural parts are suitable for the purpose, reliable and


B) all the components are properly integrated and assembled in an appropriate manner
.

2.9 Filling and draining

Where applicable, pressure equipment must be designed and
equipped with accessories or measures must be taken for its
installation, to ensure safe filling and discharge
equipment, particularly with regard the risks such

A) the performance

I) overfilling or excessive pressure, particularly with regard to the degree of fulfillment and
vapor pressure at the reference temperature and

Ii) the instability of the pressure device

B) on discharge: the uncontrolled release of the pressurized fluid and

C) on filling or discharge: unsafe connection and disconnection.

2.10 Protection against exceeding the allowable limits of pressure equipment

If, under reasonably foreseeable conditions could lead to

Exceeding the allowable limits, pressure equipment must be fitted with suitable protective devices or
measures must be taken for their
installation, unless protection
other protective devices within an assembly.

Suitable device or combination of such devices must
designed based on the specific characteristics of the equipment or assembly
.

Suitable protective devices and combinations thereof comprise

) Safety accessories, or

B) appropriate monitoring equipment, such as indicators
devices that allow it to be performed automatically or manually
appropriate intervention, whereby keep the pressure equipment within the allowable limits
.

2.11 Safety equipment

2.11.1 Safety accessories must

A) be designed and constructed so as to be reliable and suitable for their intended function
and take into account any requirements for the maintenance and testing
these devices

B) be independent of other functions, unless such other functions
not be affected safety functions and

C) comply with the relevant principles of design in order to obtain suitable and reliable protection
. These principles include notably the principle of safe mode
fail, redundancy, diversity and self-diagnosis.

2.11.2 Pressure limiting devices

These devices must be designed so that no permanent
exceed the maximum allowable pressure PS;
any short-term increase in pressure is allowable, if it occurs under conditions
specified in 7.3.

2.11.3 Temperature monitoring devices

These devices must have safety reasons adequate response time,
which is in accordance with the measurement function.

2.12 External fire

Where necessary, pressure equipment must be designed and, where
fitted with suitable accessories, or must be taken to his
fitting, to meet damage-limitation requirements in the event of external
fire with due regard to its intended use.

Third PRODUCTION

3.1 Production processes

Manufacturer must ensure the competent execution of the measures that have been taken in
design stage by applying the appropriate techniques and relevant procedures,
particularly with regard to the following elements.

3.1.1 Production of components

In the manufacture of components, for example forming and chamfering,
not give rise to defects or cracks or changes in the mechanical properties
that could endanger the safety of the equipment.
3.1.2 Permanent joining


Permanent joints and adjacent zones must be free of any
surface or internal defects that could endanger the safety device
.

Properties of permanent joints must meet the minimum
properties specified for the materials to be joined, if not at
design calculations intentionally taken into account the value
other relevant characteristics.

For pressure equipment must be
permanent joining of components which contribute to the resistance against pressure and
components which are directly attached to them, made
suitable qualified personnel using appropriate job
procedures.

For pressure equipment in categories II, III and IV must be working procedures and relevant personnel
approved by a competent third party which, according to the manufacturer's choice
may be

A) notified body or

B) recognized by an independent organization.

For purposes of this approval by independent organizations must perform
examinations and tests specified in the relevant harmonized standards
or equivalent examinations and tests.
3.1.3 Non-destructive testing


Destructive tests of permanent joints of pressure equipment
carried out by staff with relevant qualifications.

For pressure equipment in categories III and IV, the personnel must be approved
recognized by an independent organization.

3.1.4

Where there is a risk that the manufacturing process will change the material properties
to an extent that could jeopardize the safety of the equipment must be
at an appropriate stage suitable heat treatment.
3.1.5 Traceability


It is necessary to establish and maintain appropriate procedures for identifying materials
components of the equipment which contribute to its
pressure resistance by suitable means from
receipt, through production up to the final test of the manufactured
pressure equipment.

3.2 Final assessment

Pressure equipment must be subjected to final assessment as described below.

3.2.1 Final inspection

Pressure equipment must undergo a final inspection, in which the

Based on visual inspection of accompanying documents
compliance with the requirements of this Regulation. In doing so shall also be paid to
tests performed during production. If it's for security reasons
necessary shall be final check carried out internally and externally on every part
equipment, where appropriate in the course of production, for example
where inspection is not possible during the final inspection.
3.2.2 Pressure test


Final assessment of pressure equipment must be tested
pressure resistance, which will normally take the form of a hydrostatic pressure test
pressure at least equal, if it comes in
account, the value specified in 7.4.

U series-produced pressure equipment category I may be the
test performed on a statistical basis.

Where the hydrostatic pressure test is harmful or impractical,
can be made equivalent tests. For other tests
than the hydrostatic pressure test is required prior to their implementation
implement additional measures, such as non-destructive tests or other methods of equivalent
.

3.2.3 Inspection of safety devices

For assemblies, the final assessment must also include a check
safety devices intended to check full compliance with the requirements set out in paragraph
2.10

3.3 Marking and labeling

In addition to the CE marking in accordance with § 15 and putting information in accordance with § 6.
5 and § 8 par. 3 must contain the following information:

A) for all pressure equipment

I) the year of manufacture,

Ii) identification of the pressure equipment according to its nature, such
identification of type, serial or batch and serial number and

Iii) the essential maximum / minimum allowable limits,

B) depending on the type of pressure equipment, further information necessary for
safe installation, operation or use and, where applicable, maintenance and periodic inspections
like

I) the volume of the pressure equipment in liters

Ii) nominal size DN,

Iii) the test pressure PT applied in bar exam dates,

Iv) the safety device set pressure in bar,

V) the performance of the pressure equipment in kW,

Vi) supply voltage in V (volts)

Vii) the intended use,

Viii) the degree of filling kg / L,

Ix) the greatest mass content in kg

X) empty weight in kg and

Xi) fluid group,

C) where necessary, warnings fixed to the pressure equipment
drawing attention to misuse which experience has shown might occur
.

The information referred to in subparagraphs a), b) and c) must be given on the pressure
facility or on a label firmly attached to it, with the following exceptions
:

I) where applicable, may be used, appropriate documentation to
avoid repetitive marking of individual parts, for example
piping components, intended for the same assembly,

Ii) if it is too small, eg accessories, the
this information may be given on a label attached to that pressure equipment and


Iii) information on the mass to be filled and the warnings referred to in subparagraph c)
may be listed on the label or other appropriate means, provided that they remain legible
for a sufficiently long period of time.

3.4 Instructions for use

A) When pressure equipment available on the market, must be treated as if it is needed
, accompanied by instructions for the user, containing all the necessary information
relating to safety and concerning:

I) installation, including assembling of different pieces of pressure equipment

Ii) commissioning

Iii) use and

Iv) maintenance, including checks by the user.

B) The instructions must contain the information posted on the pressure equipment
in accordance with paragraph 3.3, with the exception of serial identification, and must be accompanied, where appropriate
technical documents, drawings and diagrams necessary for a full understanding of
instructions.

C) The instructions must, if necessary, also highlighting the risks resulting from the improper use
set out in section 1.3 and on special terms
design in accordance with 2.2.3.

Fourth MATERIALS

The materials used for the manufacture of pressure equipment must be suitable for such use
throughout the planned life of them, unless
replacement.

Welding consumables and other joining materials need
adequately fulfill only the relevant requirements set out in paragraph 4.1
, point 4.2. ) and the first paragraph of 4.3, and
both individually and in a joined structure.

4.1 Materials for pressurized parts

A) have appropriate properties for all operating conditions that can
reasonably foreseeable and for all test conditions, especially
be sufficiently ductile and tough. If applicable, must

Material properties meet the requirements set out in Section 5.7
In addition, it is necessary to pay particular attention to the selection of materials that
to prevent brittle fracture, if necessary;
if the special need to use brittle material must be appropriate
measures

B) be sufficiently chemically resistant to the fluid contained in the
pressure equipment; during the planned life of the equipment must not be significantly affected
chemical and physical properties necessary for
safety,

C) not be significantly affected by aging,

D) be suitable for the intended processes and

E) they are selected so that the mutual bonding various materials
avoid significant undesirable effects.
4.2
pressure equipment manufacturer

A) defines an appropriate manner the values ​​necessary for the design calculations
set out in Section 2.2.3 and the basic properties of materials and their processing
specified in paragraph 4.1

B) provide in his technical documentation elements relating to compliance with
materials specifications of this Regulation one of the following ways
:

I) using materials which are in conformity with harmonized standards,

Ii) using materials covered by a European approval
pressure equipment materials in accordance with § 12, or

Iii) the specific assessment materials and

C) for pressure equipment in categories III and IV, particular appraisal
materials performed by the notified body responsible for the conformity assessment procedures
pressure equipment.

4.3 The equipment manufacturer must take appropriate measures to ensure that the material used
accordance with specified requirements. In particular it must be for all
Materials available documentation prepared by the manufacturer that
affirming compliance with the specification.

For the main pressure-bearing parts of equipment in categories II, III and IV
must take the form of a certificate of specific product control
.

Where a material manufacturer has an appropriate quality assurance system,
certified by a competent body established within the European Union and
undergone a specific assessment for materials, shall be considered
certificates issued by the manufacturer to certify conformity with the relevant requirements
this point.

SPECIFIC PRESSURE EQUIPMENT REQUIREMENTS

Addition to the applicable requirements set out in paragraphs 1-4 to the pressure
equipment referred to in paragraphs 5 and 6, subject to the following requirements.

Fifth PRESSURE EQUIPMENT FIRED OR OTHERWISE HEATED WITH RISK OF OVERHEATING
under § 3 para. 2

This pressure equipment includes

1) steam and hot water generators under § 3 para. 2 point. b) as
fired steam and hot water boilers, heaters and
reheaters, waste heat boilers, waste incineration boilers, electric boilers heated
electrodes or with an immersion heater, pressure cookers
together with their accessories and where applicable their systems for treatment
feedwater and for fuel supply and

2) technological heating equipment for other than steam generating and
hot water under § 3 para. 2 point. a), such as heaters for
chemical and other similar processes and pressurized processing equipment
food.

This pressure equipment must be calculated, designed and constructed so that
to avoid to minimize risks of a significant loss
pressure resistance due to overheating. In particular it must be where it
applicable, provided that:

A) provide appropriate protection means for limiting
operating parameters, such as limiting intake or heat, or the level
fluid so as to avoid any risk of local and general overheating
,

B) where it is needed, the available sampling points
allow evaluation of the properties of the fluid so as to avoid the risk
related to deposits or corrosion

C) appropriate measures are taken to eliminate risks of damage from deposits
,

D) the available means of safe removal of residual heat
after weaning and

E) steps are taken to prevent the accumulation of ignitable mixtures of combustible substances
and air, or flame blowback.

6th PIPING under § 3 para. 2 point. c)

Design and construction must ensure that

A) the risk of overstressing from inadmissible free movement or excessive forces arising
example, flanges, bellows or hoses
adequately controlled by means such as support, constraint,
anchoring, alignment and pre-tension ,

B) where there is a possibility that inside pipes for gaseous fluids
occur, means are provided for drainage and
removal of deposits from low areas to

Avoid damage from water hammer or corrosion,

C) has been properly taken into account the potential damage from turbulence and formation of vortices
; At the same time the relevant parts of 2.7,

D) that due consideration is given to the risk of fatigue due to vibrations in pipes
,

E) where the pipe contains a liquid Group 1 are available
appropriate means to ensure sampling pipes the size
constitutes a considerable risk

F) that is minimized the risk of accidental release;
taking place side must be clearly marked indication of the fluid contained
and

G) that the position and route of underground piping is at least in
technical documentation to facilitate safe maintenance, inspection and repair
.

7th SPECIFIC QUANTITATIVE REQUIREMENTS FOR CERTAIN PRESSURE EQUIPMENT

Usually the following provisions shall apply. However, if you do not apply
including in cases where materials are not specifically provided for and not used
harmonized standards, the manufacturer demonstrates that appropriate measures are taken
to achieve an equivalent overall level of safety.

Provisions referred to in this section supplement the essential safety
requirements set out in Sections 1 to 6 for the pressure equipment to which
apply.
7.1 Allowable stresses

7.1.1 Brands


R e / t, yield limit, indicates the value at the calculation temperature:

A) upper flow limit for a material presenting upper and lower flow,

B) the proof stress at 1.0% for austenitic steel and non-alloyed aluminum and


C) the proof stress at 0,2% in other cases.

R m / 20 indicates the minimum value of the ultimate strength at 20 ° C.

R m / t designates the ultimate strength at the calculation temperature.

7.1.2 permissible general membrane stress for predominantly static
load and at temperatures outside the range in which there is a significant
flow must not exceed the smaller of the following values, depending on the material used
:

A) in the case of ferritic steel including normalized (normalized
rolled) steel and excluding fine-grained steel and specially heat-treated steel
: 2/3 R e / t and 5/12 R m / 20 || |
B) in the case of austenitic steel:

I) either if its elongation greater than 30%: 2/3 R e / t

Ii) or, alternatively, if the elongation exceeds 35%, 5/6 R e / t
1/3 R m / t

C) in the case of unalloyed or low-alloy cast steel, 10/19 R
e / t and 1/3 of R m / 20

D) in the case of aluminum, 2/3 R e / t

E) in the case of hardening aluminum alloys: 2/3 R e / t and 5/12 R
m / 20.

7.2 Joint coefficients

For welded joints, the joint coefficient must not exceed the following values ​​
:

A) for equipment subject to destructive and non-destructive tests
which confirm that the whole series of joints show no significant defects:
1

B) for equipment subject to random non-destructive testing: 0.85 and

C) for equipment not subject to non-destructive testing other than visual inspection
: 0.7.

If necessary, it is necessary to take into consideration also the type of stress and the mechanical and technological properties
joint.

7.3 Pressure limiting devices, particularly for pressure vessels

Momentary pressure specified in paragraph 2.11.2 shall not exceed 10%
value of the maximum allowable pressure.

7.4 Hydrostatic test pressure

For pressure vessels must be hydrostatic test pressure specified in paragraph 3.2.2
smaller than some of the following values:

A) the maximum load pressure, which may be subjected to pressure
equipment in operation with respect to the maximum allowable pressure
a maximum allowable temperature of the pressure device, multiplied by 1.25 and


B) the maximum allowable pressure multiplied by the coefficient 1.43.
7.5 Material properties


If by any other criteria other values ​​are required, which is
be taken into account, steel is considered as sufficiently ductile to satisfy
requirements set out in section 4.1 point. a) if, in a tensile test carried
standard procedure, its elongation value of less than 14%
and its impact strength test Impact bending measured on a test
rod with a V notch ISO is not less than 27 J at a temperature which does not exceed
20 ° C but not higher than the lowest anticipated
working temperature.


Příl.2

CONFORMITY ASSESSMENT TABLES
First The categories mentioned in the charts for the following modules:
For category I: module A
For category II modules A2, D1, E1
For category III: Module B (design type) + D module B ( design type) + F
Module B (production type) + E Module B (production type) + C2, modulH
For category IV: Module B (production type) + D module B (production type) + F, module G

Module H1

Second Safety equipment referred to in § 3 para. 2 point. d)
is classified in category IV.

Based on the exemption may be safety accessories manufactured for specific equipment
classified in the same category as the equipment they protect
.

Third Pressure equipment referred to in § 3 para. 2 point. d) is classified in the classification by
:

A) their maximum allowable pressure PS

B) their volume V or their nominal size DN and

C) group of fluids for which they are intended.

To determine the conformity assessment category applies
appropriate table for vessels or piping.

If, pursuant to subparagraph b) comes into consideration both the volume and the nominal
diameter, pressure accessory must be classified in the category that is higher
.

Fourth The following graphs for conformity assessment demarcation lines
upper limit for each category.
Graph 1


Containers under § 3 para. 2 point. a) point 1.1

Exception containers are intended for unstable gases and falling by
graph 1 to category I or II, which must be classified in category III
.

Graph 2


Containers under § 3 para. 2 point. a) point 1.2

Exceptionally, portable extinguishers and bottles for breathing equipment
must be classified at least in category III.

Chart 3


Containers under § 3 para. 2 point. a) Section 2.1

Graph 4


Containers under § 3 para. 2 point. a) Section 2.2

Exceptionally, assemblies intended for generating warm water under § 3 para. 3
point. b) which must be submitted to either the EU-type examination (Module B -
design type), with respect to their compliance with the essential requirements
set out in paragraphs 2.10, 2.11 and 3.4, and in point 5. a) d) of Annex
No. 1 hereto, or full quality assurance (module H).

Chart 5


Pressure equipment under § 3 para. 2 point. b)

Exceptions are pressure cookers, the proposal must be subjected to the process
conformity assessment procedure equivalent to at least one of the modules
category III.

Chart 6


Pipeline under § 3 para. 2 point. c) point 1.1

Exceptionally, piping intended for unstable gases and falling by 6
chart to category I or II, which must be classified in category III
.

Figure 7


Pipeline under § 3 para. 2 point. c) point 1.2

Exception piping containing fluids at a temperature greater than 350 ° C and falling
according to chart 7 in category II, which must be classified in category III
.

Figure 8


Pipeline under § 3 para. 2 point. c) Section 2.1

Chart 9


Pipeline under § 3 para. 2 point. c) Section 2.2



Příl.3

CONFORMITY ASSESSMENT PROCEDURES
Provisions for pressure equipment under this Annex also apply to
report.

First INTERNAL PRODUCTION CONTROL (MODULE A)

First Internal production control is the conformity assessment procedure whereby the manufacturer
performs the activities specified in paragraphs 2, 3 and 4, and ensures and
issued a statement that the pressure equipment satisfies the requirements of this regulation.

Second Technical documentation

The manufacturer shall establish the technical documentation.

Technical documentation must enable the conformity of the pressure equipment
with the relevant requirements and include an adequate analysis and assessment
risk. The technical documentation shall specify the requirements and the extent
necessary for the assessment must cover the design, manufacture and operation
pressure equipment. The technical documentation must include, if applicable
least the following details:

A) a general description of the pressure device

B) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

C) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

D) list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

E) results of design calculations, examinations carried out
and

F) test.

Third Production

The manufacturer shall take all measures necessary so that the manufacturing process and its monitoring ensure conformity
manufactured pressure equipment with the technical documentation
under point 2 and with the requirements of this Regulation.

Fourth CE marking and EU declaration of conformity

4.1 The manufacturer shall affix the CE marking on each individual pressure equipment
which meets the relevant requirements of this Regulation.

4.2 The manufacturer must draw up the model of the pressure device written EU

Declaration of conformity for 10 years from putting pressure equipment on the market
together with the technical documentation for the needs of
supervision. The EU declaration of conformity indicated pressure equipment for which
been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

Fifth Authorised representative

Activities producers set out in point 4 may be his name and on his
responsibility, by his authorized representative, if they are listed in
credentials.

Second INTERNAL CONTROL OF PRODUCTION WITH PRESSURE CHECKS under supervision in
RANDOM INTERVALS (MODULE A2)

First Internal production control with monitoring of pressure equipment under the supervision of
random intervals is the conformity assessment procedure whereby the manufacturer
performs the activities specified in paragraphs 2, 3, 4 and 5, and ensures and
issued a statement that the pressure equipment meets the requirements of this regulation
.

Second Technical documentation

The manufacturer shall establish the technical documentation.
Documentation must allow assessment of the conformity of the pressure equipment with the relevant requirements and includes
adequate analysis and risk assessment.
Technical documentation shall specify the requirements and to the extent necessary for the assessment must
cover the design, manufacture and operation of the pressure device.
The technical documentation must include, if applicable, at least the following information:

A) a general description of the pressure device

B) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

C) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

D) list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

E) results of design calculations, examinations, and


F) test.

Third Production

The manufacturer shall take all measures necessary so that the manufacturing process and its monitoring ensure compliance
manufactured pressure equipment with the technical documentation referred
point 2 and with the requirements of this regulation, which will apply to them
.

Fourth Final assessment and inspection of pressure equipment

Manufacturer performs final assessment pressure equipment which form
checks unannounced visits by the notified body chosen by the manufacturer.

Notified body must carry or have carried out product checks at random intervals selected
laid down by it to verify the quality of internal controls
pressure equipment, taking into account inter alia the technological complexity
pressure equipment and the quantity of production .

During unannounced visits, the notified body

A) verify that the manufacturer actually performs final assessment in accordance with section 3.2 of Annex
no. 1 hereto and

B) take samples of pressure equipment at the manufacturing or storage
premises in order to perform the tests.

Notified body assesses the number of items of equipment to sample and
whether these samples is necessary to perform or have performed, all
final assessment or part thereof.

Procedure to determine the acceptability of the samples to be used should be
determine whether the manufacturing process of the pressure device runs within acceptable limits
to ensure their compliance.

In the event that one or more of the pressure equipment or assemblies in
not conform, the notified body must take appropriate measures.

Manufacturer under the responsibility of the notified body placed during the manufacturing process
identification number to each individual.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking on each individual pressure equipment
which meets the relevant requirements of this Regulation.

5.2 The manufacturer must draw up the model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
together with the technical documentation for the needs of
supervision. The EU declaration of conformity indicated pressure equipment for which
been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

6th Authorised representative

Activities producers set out in point 5 may be his name and on his
responsibility, by his authorized representative, if they are listed in
credentials.

Third EU type examination (Module B)

3.1 EU production type examination

First EU production type examination is the part of a conformity assessment procedure in
notified body examines the technical design of the pressure equipment

Verifies and attests that the technical design
pressure equipment meets the requirements of this regulation.

Second EU production type examination is to assess the suitability of technological
pressure equipment design
through examination of the technical documentation and supporting evidence referred to in Section 3 and examination of a sample
full of pressure equipment representative for the planned
production.

Third Manufacturer with a single notified body of his choice for
EU-type examination. The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) a written declaration that the same application has not been lodged with another notified body and


C) technical documentation. Technical documentation must enable
conformity assessment of pressure equipment with the requirements of this regulation and
include an adequate analysis and risk assessment.
The technical documentation shall specify the requirements and to the extent necessary for
assessment must cover the design, manufacture and operation of the pressure device
. The technical documentation must include, if applicable,
least the following information:

I) a general description of the pressure device

Ii) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

Iii) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

Iv) a list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

V) results of design calculations, examinations carried out,

Vi) test reports,

Vii) information concerning the tests in production

Viii) information regarding the qualifications or approvals required under
set out in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto,

Ix) the specimens representative of the production envisaged.
Sample may include several versions of pressure equipment provided that the differences between the versions
do not affect the level of safety. The notified body may request further samples
if it is required to perform the test program and

X) supporting evidence for the suitability of the technical solutions adopted in the draft.
This supporting evidence shall mention any documents that have been
used, in particular where the relevant harmonized standards have not been applied in its entirety
. The supporting evidence shall include, if necessary
results of tests carried out by the appropriate laboratory of the manufacturer claiming
other relevant technical specifications or other testing laboratory
his behalf and under his responsibility.

Fourth The notified body

4.1 examine the technical documentation and supporting evidence to assess the adequacy of the technical
pressure equipment design and manufacturing processes.

Particular the notified body

A) assess the materials where these are not in conformity with the relevant
harmonized standards or with a European approval for materials
pressure equipment, and verify the certificate issued by the material manufacturer in
accordance with paragraph 4.3 of Annex . 1 hereto,

B) approve the procedures for the permanent joining of
or check whether they have been previously approved in
accordance with paragraph 3.1.2 of Annex no. 1 hereto and

C) verify that the personnel undertaking the permanent joining of pressure equipment
and non-destructive tests are qualified or
approved in accordance with sections 3.1.2 and 3.1.3 of Annex no. 1 to this
Regulation

4.2 verifies that were manufactured in conformity with the technical documentation,
and identify the elements which have been designed in accordance with the applicable provisions
relevant harmonized standards, as well as the elements which have been designed for use
other relevant technical specifications without being
applying the relevant provisions of those standards

4.3 out the appropriate examinations and necessary tests to check whether
, where the manufacturer has chosen solutions in the relevant harmonized
standards, these standards have been applied correctly,

4.4 out the appropriate examinations and necessary tests to check whether
when not used solutions in the relevant harmonized standards
, the solutions that manufacturers applying
other relevant technical specifications the corresponding essential
safety requirements of this Regulation and

4.5 agree with the manufacturer, the location where the examinations and tests conducted
.

Fifth The notified body shall establish an evaluation report that records

Activities undertaken in accordance with point 4 and their outcomes.
Without prejudice to the obligations of the notified body to the notifying authority, announced
body shall release the content of this report, in whole or in part,
only with the consent of the manufacturer.

6th Where the type meets the requirements of this regulation shall issue a certificate to the manufacturer
EU production type examination. Without prejudice to paragraph 7
certificate is valid for 10 years with renewal options and includes
name and address of the manufacturer, conclusions of the examination, conditions for its validity,
if they are placed, and data necessary to identify the approved type.

The certificate must be accompanied by a list of important parts of the technical
documentation and a copy kept by the notified body.

Certificate and its annexes shall contain all relevant information enabling
evaluate whether pressure equipment manufactured in compliance with
examined type and to check for traffic.

Where the type meets the relevant requirements of this Regulation, the notified body refuses to issue
EU examination certificate and production type
shall inform the applicant accordingly, giving detailed reasons for the rejection.
Must be made for an appeals procedure.

7th The notified body shall to be informed of any changes
generally acknowledged state of the art, which would indicate that the approved
type may no longer comply with the applicable requirements of this Regulation, and
decide whether these changes require additional investigation. If
investigation, the notified body shall inform the manufacturer.

The manufacturer shall inform the notified body that holds the technical
documentation relating to the EU-type examination of the production, by
all modifications to the approved type that may affect the conformity of the pressure
equipment with the essential safety requirements of this Regulation or || | conditions of its validity. Such modifications require additional approval in the form
addition to the original EU-type examination
production.

8th Each notified body shall inform the Office of the EU-examination certificates
production type or any additions thereto which it has issued or withdrawn, and
periodically or upon request, make available a list of the Office
certificates or additions thereto refused, suspended or otherwise restricted.

Each notified body shall inform the other notified bodies concerning the EU-examination certificates
production type or any additions thereto which
refused, withdrawn, suspended or otherwise restricted, and, upon request, on
certificates or additions thereto issued.

European Commission, EU Member States and the other notified bodies
notified body may ask for a copy of the certificate examination
EU production type or any additions thereto. The European Commission and the Member States of the European Union
may request a copy of the notified body
technical documentation and the results of the examinations conducted by it. Until the expiry of its validity
EU-type examination of the production kept by the notified body
copy of this certificate, its annexes and additions, as well as technical
file including the documentation submitted by the manufacturer.

9th The manufacturer shall make available to the supervisory authority a copy of the certificate examination
EU production type, its annexes and additions together with the technical
documentation for a period of 10 years from putting pressure on the market.

10th Manufacturer's authorized representative may lodge the application referred to in paragraph 3 and
perform the tasks set out in paragraphs 7 and 9, if the manufacturer in the commission
authorized representative established.

3.2 EU-type examination design

First EU design type examination is the part of a conformity assessment procedure
a notified body examines the technical design of pressure equipment
and verifies and attests that the technical design
pressure equipment meets the requirements of this regulation.

Second EU-type examination design is to assess the suitability of technological
pressure equipment design
through examination of the technical documentation and supporting evidence referred to in paragraph 3, without examination
sample.

In the context of this module you can not use an experimental method of designing
specified in paragraph 2.2.4 of Annex no. 1 hereto.

Third The manufacturer shall lodge an application for EU-type examination with a single design
notified body of his choice.

The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) a written declaration that the same application has not been lodged with another notified body and


C) technical documentation. Technical documentation must enable
conformity assessment of pressure equipment with the requirements of this regulation and
include an adequate analysis and risk assessment.
The technical documentation shall specify the requirements and to the extent necessary for
assessment must cover the design, manufacture and operation of the pressure

Equipment. The technical documentation must include, if applicable,
least the following information:

I) a general description of the pressure device

Ii) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

Iii) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

Iv) a list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

V) results of design calculations, examinations carried out,

Vi) information regarding the qualifications or approvals required under
set out in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto and

Vii) supporting evidence for the suitability of the technical solutions adopted in the draft.
This supporting evidence shall mention any documents that have been
used, in particular where the relevant harmonized standards have not been applied in its entirety
. The supporting evidence shall include, if necessary
results of tests carried out by the appropriate laboratory of the manufacturer or other
testing laboratory on his behalf and under his responsibility.

The application may cover several versions of pressure equipment provided that
differences between the versions do not affect the level of safety.

Fourth The notified body

4.1 examine the technical documentation and supporting evidence to assess the adequacy of the technical
product design.

Particular the notified body

A) assess the materials where these are not in conformity with the relevant
harmonized standards or with a European approval for materials for pressure equipment and


B) approve the procedures for the permanent joining of
or check whether they have been previously approved in
accordance with paragraph 3.1.2 of Annex no. 1 hereto;

4.2 implement appropriate examination to check whether, where the manufacturer has chosen
solutions in the relevant harmonized standards, these standards have been applied correctly
;

4.3 implement appropriate examination to ascertain whether, if it has not been used
solutions in the relevant harmonized standards, the solutions adopted by the manufacturer
corresponding essential safety requirements of this Regulation
.

Fifth The notified body shall establish an evaluation report that records
activities undertaken in accordance with point 4 and their outcomes.
Without prejudice to the obligations of the notified body to the notifying authorities, the notified body
publish the content of this report, in whole or in part,
only with the consent of the manufacturer.

6th If the proposal meets the requirements of this Regulation shall issue a certificate to the manufacturer
EU examination of the design type. Notwithstanding
point 7, the certificate is valid for 10 years with the possibility of renewal and
contains the name and address of the manufacturer, conclusions of the examination
validity of the certificate, if available, and data necessary to identify | || approved design.

The certificate must be accompanied by a list of important parts of the technical
documentation and a copy kept by the notified body.

Certificate and its annexes shall contain all relevant information enabling
evaluate whether pressure equipment manufactured in compliance with
examined design, and to check for traffic.

If the proposal does not meet the relevant requirements of this Regulation, the notified body refuses to issue
EU examination certificate design type and
shall inform the applicant accordingly, giving detailed reasons for the rejection.

7th The notified body shall to be informed of any changes
generally acknowledged state of the art, which would indicate that
approved design may no longer comply with the applicable requirements of this Regulation,
and decide whether these changes require additional investigation. If
investigation, the notified body shall inform the manufacturer.

The manufacturer shall inform the notified body that holds the technical
documentation relating to the EU's examination of the design,
of all modifications to the approved type that may affect the conformity of the pressure
equipment with the essential safety requirements of this Regulation or || | conditions of its validity. Such modifications require additional approval in the form
addition to the original EU-type examination
design.

8th Each notified body shall inform the Office of the EU-examination certificates
design type or additions thereto which it has issued or withdrawn, and
periodically or upon request, make available a list of the Office
certificates or additions thereto refused, suspended or otherwise restricted.


Each notified body shall inform the other notified bodies concerning the EU-examination certificates
design type or additions thereto
refused, withdrawn, suspended or otherwise restricted, and, upon request, also
about certificates or additions thereto issued.

European Commission, EU Member States and the other notified bodies
notified body may ask for a copy of the certificate examination
EU design type or amendments thereto. The European Commission and the Member States of the European Union
may request a copy of the notified body
technical documentation and the results of the examination conducted by him. Until the expiry of its validity
EU design type examination
notified body keeps a copy of this certificate, its annexes and additions, as well
technical file including the documentation submitted by the manufacturer.

9th The manufacturer shall make available to the supervisory authority copy of the EU
examination of the design, its annexes and additions together with
technical documentation for 10 years after the pressure equipment on the market
.

10th Manufacturer's authorized representative may lodge the application referred to in paragraph 3 and
perform the tasks set out in paragraphs 7 and 9, if the manufacturer in the commission
authorized representative established.

Fourth CONFORMITY TO TYPE BASED ON INTERNAL PRODUCTION CONTROL WITH PRESSURE CHECKS
under supervision AT RANDOM INTERVALS (MODULE C2
)

First Conformity to type based on internal production control with controls
pressure equipment under supervision at random intervals is
part of a conformity assessment procedure conducted by the manufacturer
actions specified in paragraphs 2, 3 and 4, and ensures and declares
that the pressure equipment is in conformity with the type described in the EU
examination and satisfy the requirements of this Regulation which apply to them.

Second Production

The manufacturer shall take all measures necessary so that the manufacturing process and its monitoring ensure compliance
manufactured pressure equipment with the type
described in the EU type examination certificate and with the requirements of this regulation
that apply to them.

Third Final assessment and inspection of pressure equipment

Notified body chosen by the manufacturer must perform or have performed examinations in
random intervals specified by them, in order to verify the quality
final assessment of internal controls and pressure equipment, with
into account inter alia the technological complexity of pressure
equipment and the quantity of production.

Notified body shall verify that the manufacturer actually performs final assessment
in accordance with section 3.2 of Annex no. 1 hereto.

Prior to launch removes the notified body on the spot
adequate sample of the final pressure equipment, which must be
examined and appropriate tests set out in the relevant
parts of the harmonized standards or equivalent tests using
other technical specifications in order to verify that it conforms
with the relevant requirements of this Regulation.

Notified body assesses the number of items of equipment to sample and
whether such samples of pressure equipment it is necessary to perform, or have performed, all
final assessment or part thereof.

If a sample does not acceptable quality level, the body shall take appropriate measures
.

Procedure to determine the acceptability of the samples to be used should be
determine whether the manufacturing process of the pressure device runs within acceptable limits
to ensure their compliance.

When undertaking tests by the notified body, the manufacturer during the manufacturing process
affix the responsibility of the notified body's identification number
this subject.

Fourth CE marking and EU declaration of conformity

4.1 The manufacturer shall affix the CE marking on each
pressure equipment or assembly, which are in conformity with the type described in the EU
type examination and satisfy the requirements of this Regulation.

4.2 The manufacturer must draw up the model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

Fifth Authorised representative

Activities producers set out in point 4 may be his name and on his
responsibility, by his authorized representative, if the manufacturer in
commission authorized representative established.

Fifth CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTION PROCESS
(MODULE D)

First Conformity to type based on quality assurance of the production process is
part of a conformity assessment procedure conducted by the manufacturer
actions specified in paragraphs 2 and 5, and ensures and declares that the
pressure equipment or assembly are in compliance with type as described in

EU type examination certificate and satisfy the requirements of this regulation,
which apply to them.

Second Production

The manufacturer shall operate an approved quality system for production, final inspection and testing of the
pressure equipment referred to in paragraph 3 and is subject
oversight as provided in section 4.

Third Quality system

3.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) a written declaration that the same application has not been lodged with another
notified body

C) all relevant information on the expected type of pressure
device

D) the documentation concerning the quality system and

E) the technical documentation of the approved type and a copy of the certificate
EU-type examination.

3.2 The quality system must ensure compliance of the pressure equipment with the type
described in the EU type examination certificate and with the requirements of this regulation
that apply to them.

All the elements, requirements and provisions adopted by the manufacturer must be
documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description of:

A) objectives in terms of quality and organizational structure, responsibilities and powers of the management
regarding the quality of the pressure equipment

B) appropriate methods, processes and systematic actions that
used in manufacturing, quality control and quality assurance, particularly
operating procedures used for the joining of parts,
approved in accordance with paragraph 3.1.2 Annex no. 1 hereto,

C) examination and tests that will be carried out before, during
and after manufacture, the frequency with,

D) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications or approvals of the workers, especially workers who perform
joining of parts and
destructive tests specified in paragraphs 3.1.2. and 3.1.3. Annex no. 1 hereto and

E) the means of supervising the achievement of the required quality and
the effective operation of the quality system.

3.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 3.2.

The elements of the quality system that comply with the corresponding specifications
relevant harmonized standards, compliance with these requirements.

Person who on behalf of the notified body carried out conformity assessment (hereinafter referred
"engagement team") must have experience in quality management systems and
least one member must have experience of evaluation in the relevant field of pressure
equipment and technology evaluation of the pressure
equipment and knowledge of the applicable requirements of this Regulation.
The audit includes an assessment visit to the manufacturer's premises.

Audit team to examine the technical documentation specified in paragraph 3.1
point. e) to verify the manufacturer's ability to identify the relevant requirements of this Regulation
and carry out the necessary checks to ensure compliance
pressure equipment with these requirements.

Conclusions of the audit and the reasons are notified to the manufacturer.

3.4 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

3.5 The manufacturer shall inform the body which approved the quality system
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in paragraph 3.2,
or whether a reassessment is necessary.

It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

Fourth Supervision notified body

4.1 The purpose of supervision is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

4.2 For assessment purposes, allow the manufacturer to the notified body access to
locations of manufacture, inspection, testing and storage and provide
it with all necessary information, in particular

A) the quality system documentation and

B) the quality records, such as inspection reports, records of tests performed
records of calibrations performed, reports on the qualifications of the personnel
.

4.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer report

Audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.

4.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
. The need and frequency of these additional visits will be determined on the basis
management system of inspection visits
used by the notified body.

This system must take into account the following factors:

A) category of pressure equipment

B) the results of previous visits,

C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system is working properly
. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in section 3. 1 on each individual pressure equipment
which is in conformity with the type described in the EU type examination certificate and satisfies the applicable requirements
this Regulation.

5.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

6th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) the documentation specified in paragraph 3.1

B) the change referred to in paragraph 3.5, as approved and

C) the decisions, reports and reports from the notified body
set out in paragraphs 3.3, 3.5, 4.3 and 4.4.

7th Each notified body shall inform the Authority for approval of a quality system
issued or withdrawn, and shall, periodically or upon request, make available a list of the Office
quality system, which it has refused, suspended or otherwise restricted
.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended, withdrawn or otherwise restricted
, and at the request of quality system approvals issued.

8th Authorised representative

Activities producers set out in paragraphs 3.1, 3.5, 5 and 6 may be
his behalf and under his responsibility, by his authorized representative if
manufacturer in the commission authorized representative established.

6th QUALITY ASSURANCE OF THE PRODUCTION PROCESS (Module D1)

First Quality assurance of the production process is the conformity assessment procedure
whereby the manufacturer performs the activities set out in paragraphs 2, 4 and 7
ensures and declares that the pressure equipment
meet the requirements of this Regulation which apply to them .

Second Technical documentation

The manufacturer shall establish the technical documentation.
Documentation must allow assessment of the conformity of the pressure equipment with the relevant requirements and includes
adequate analysis and risk assessment.
Technical documentation shall specify the requirements and to the extent necessary for the assessment must
cover the design, manufacture and operation of the pressure device.
The technical documentation must include, if applicable, at least the following information:

A) a general description of the pressure device

B) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

C) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

D) list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

E) results of design calculations, examinations carried out
and

F) test.

Third Manufacturer of technical documentation shall make available to the supervisory authority
over a period of 10 years from putting pressure on the market.

Fourth Production

The manufacturer shall operate an approved quality system for production, final inspection and testing
of the pressure device according to claim 5, and subject to supervision under point 6


Fifth Quality system

5.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address


B) a written declaration that the same application has not been lodged with another
notified body

C) all relevant information on the expected type of pressure
device

D) the documentation concerning the quality system and

E) technical documentation as set out in section 2

5.2 The quality system must ensure compliance of the pressure equipment with
requirements of this Regulation which apply to them.

All the elements, requirements and provisions adopted by the manufacturer must be
documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description

A) objectives in terms of quality and organizational structure, responsibilities and powers of the management
regarding the quality of the pressure equipment

B) appropriate methods, processes and systematic actions that
used in manufacturing, quality control and quality assurance, particularly
operating procedures used for the joining of parts,
approved in accordance with paragraph 3.1.2 Annex no. 1 hereto,

C) examination and tests that will be carried out before, during
and after manufacture, the frequency with,

D) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications of the workers, especially workers who carry
joining of parts in accordance with paragraph 3.1 .2 Annex no. 1 to this Regulation and


E) the means of supervising the achievement of the required quality
product and the effective operation of the quality system.

5.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 5.2. The elements of the quality system by
conform to the relevant harmonized standards conform to the relevant
requirements set out in section 5.2 is assumed.

The assessment team must have experience in quality management systems and
least one member must have experience of assessments of the technology
pressure equipment and knowledge of the applicable requirements of this Regulation.
Audit includes an assessment visit to the manufacturer's premises.

Audit team to examine the technical documentation specified in paragraph 2
to verify the manufacturer's ability to identify the relevant requirements of this Regulation and
carry out the necessary checks to ensure compliance
pressure equipment with these requirements.

Conclusions of the audit and the reasons are notified to the manufacturer.

5.4 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

5.5 The manufacturer shall inform the body which approved the quality
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in Section 5.2,
or whether a reassessment is necessary.

It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

6th Supervision notified body

6.1 The purpose of surveillance is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

6.2 For assessment purposes, allow the manufacturer to the notified body access to
locations of manufacture, inspection, testing and storage and provide
it with all necessary information, in particular:

A) quality system documentation,

B) technical documentation as set out in Section 2

C) quality records, such as inspection reports, records of tests performed
records of calibrations performed, reports on the qualifications of the personnel
.

6.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer
report on the audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.

6.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
. The need and frequency of these additional visits will be determined on the basis
management system of inspection visits
used by the notified body.

This system must take into account the following factors:

A) category of pressure equipment

B) the results of previous visits,

C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system properly

Works. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

7th CE marking and EU declaration of conformity

7.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 5.1 on each individual pressure equipment
which is in conformity with the relevant requirements of this Regulation.

7.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity
identify the product model for which it was drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

8th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) the documentation specified in paragraph 5.1

B) the change referred to in paragraph 5.5 and

C) the decisions, reports and reports from the notified body
set out in paragraphs 5.5, 6.3 and 6.4.

9th Each notified body shall inform the Authority for approval of a quality system
issued or withdrawn, and shall, periodically or upon request, make available a list of the Office
quality system, which it has refused, suspended or otherwise restricted
.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended or withdrawn, and
at the request of quality system approvals issued.

10th Authorised representative

Activities producers set out in paragraphs 3, 5.1, 5.5, 7 and 8 may be
his behalf and under his responsibility, by his authorized representative if
manufacturer in the commission authorized representative established.

7th Conformity to type based on quality assurance of pressure equipment
(MODULE E)

First Conformity to type based on quality assurance
pressure equipment is part of a conformity assessment procedure conducted by the manufacturer
actions specified in paragraphs 2 and 5, and ensures and declares that a given
pressure equipment is in conformity with the type described
EU certificate examination and satisfy the requirements of this regulation, which will apply to them
.

Second Production

The manufacturer shall operate an approved quality system for final inspection and testing of the
pressure equipment in point 3 and subject to supervision under section 4.


Third Quality system

3.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) a written declaration that the same application has not been lodged with another
notified body

C) all relevant information on the expected type of pressure
device

D) the documentation concerning the quality system and

E) the technical documentation of the approved type and a copy of the certificate
EU-type examination.

3.2 The quality system must ensure compliance of the products with the type described in
EU type examination certificate and the appropriate requirements of this regulation
.

All the elements, requirements and provisions adopted by the manufacturer must be
documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description

A) objectives in terms of quality and organizational structure, responsibilities and powers of the management
terms of product quality,

B) the examination and tests that will be carried out after manufacture,

C) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications or approvals of the workers, especially workers who perform
joining of parts and
destructive tests specified in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto and

D) the means to the efficient operation of the system
quality.

3.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 3.2. The elements of the quality system by
corresponding specifications relevant harmonized standards
compliance with these requirements.

The assessment team must have experience in quality management systems and
least one member must have experience of evaluation in the relevant
pressure equipment and the assessment of pressure equipment technology concerned
and knowledge of the applicable requirements of this Regulation.
The audit includes an assessment visit to the manufacturer's premises. The audit team
examine the technical documentation specified in paragraph 3.1 point. e)
to verify the manufacturer's ability to identify the relevant requirements of this Regulation

And carry out the necessary checks to ensure compliance of the pressure equipment
with these requirements.

Conclusions of the audit and the reasons shall notify the manufacturer.

04.03 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

3.5 The manufacturer shall inform the body which approved the quality system
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in paragraph 3.2,
or whether a reassessment is necessary.

It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

Fourth Supervision notified body

4.1 The purpose of supervision is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

4.2 For assessment purposes, allow the manufacturer to the notified body access to
locations of manufacture, inspection, testing and storage and provide
it with all necessary information, in particular

A) quality system documentation,

B) technical documentation and

C) quality records, such as inspection reports, records of tests performed
records of calibrations performed, reports on the qualifications of the personnel
.

4.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer
report on the audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.

4.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
.

Need and frequency of these additional visits will be determined on the basis
management system audit visits used by the notified body.
This system must take into account the following factors:

A) category of pressure equipment

B) the results of previous visits,

C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system is working properly
. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 3.1 on each individual pressure equipment
which is in conformity with the type described in the EU type examination certificate and
meets the relevant requirements of this Regulation .

5.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity
identify the product model for which it was drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

6th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) the documentation specified in paragraph 3.1

B) the change referred to in paragraph 3.5, as approved and

C) the decisions, reports and reports from the notified body
set out in paragraphs 3.3, 3.5, 4.3 and 4.4.

7th Each notified body shall inform the Authority for approval of a quality system
issued or withdrawn, and shall, periodically or upon request, make available a list of the Office
quality system, which it has refused, suspended or otherwise restricted
.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended or withdrawn, and
at the request of quality system approvals issued.

8th Authorised representative

Activities producers set out in paragraphs 3.1, 3.5, 5 and 6 may be
his behalf and under his responsibility, by his authorized representative if
manufacturer in the commission authorized representative established.

8th QUALITY ASSURANCE OF FINAL CHECKS AND TESTING OF PRESSURE EQUIPMENT
(Module E1)

First Quality assurance of final inspection and testing of pressure equipment
is the conformity assessment procedure whereby the manufacturer performs
activities set out in paragraphs 2, 4 and 7, and ensures and declares that the pressure
satisfy the requirements of this regulation, which They apply to them.

Second Technical documentation

The manufacturer shall establish the technical documentation.
Documentation must allow assessment of the conformity of the pressure equipment with the relevant requirements and includes
adequate analysis and risk assessment.
Technical documentation shall specify the requirements and to the extent necessary for the assessment must

Cover the design, manufacture and operation of the pressure device.
The technical documentation must include, if applicable, at least the following information:

A) a general description of the pressure device

B) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

C) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

D) list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

E) results of design calculations, examinations carried out
and

F) test.

Third Manufacturer keeps technical documentation at the disposal of the supervisory authority
over a period of 10 years from putting pressure on the market.

Fourth Production

The manufacturer shall operate an approved quality system for final inspection and testing
of the pressure device according to claim 5, and subject to supervision under section 6.


Fifth Quality system

5.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) a written declaration that the same application has not been lodged with another
notified body

C) all relevant information on the expected type of pressure
device

D) the documentation concerning the quality system and

E) technical documentation as set out in section 2

5.2 The quality system must ensure compliance of the pressure equipment with
requirements of this Regulation which apply to them.

As part of the quality system must be inspected every pressure equipment and
must undergo appropriate tests as set out in the relevant standard or standards
according to § 13, or equivalent tests, and particularly final assessment
set out in section 3.2 of Annex no. 1 hereto,
order to ensure its conformity with the requirements of this Regulation which apply to them.

All the elements, requirements and provisions adopted by the manufacturer must be
documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description of:

A) objectives in terms of quality and organizational structure, responsibilities and powers of the management
regarding the quality of the pressure equipment

B) operating procedures used for the joining of parts,
approved in accordance with section 3.1.2 of Annex no. 1 hereto,

C) examination and tests that will be carried out after manufacture,

D) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications or approvals of the personnel, especially personnel
carrying out the joining of parts set
in paragraph 3.1.2 of Annex no. 1 hereto and

E) the means to the efficient operation of the system
quality.

5.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 5.2.

The elements of the quality system that comply with the corresponding specifications
relevant harmonized standards, compliance with these requirements.

The assessment team must have experience in quality management systems and
least one member must have experience of evaluation in the relevant
pressure equipment and the assessment of pressure equipment technology concerned
and knowledge of the applicable requirements of this Regulation.
The audit includes an assessment visit to the manufacturer's premises. The audit team
examine the technical documentation specified in paragraph 2 to verify that
ability to identify the relevant requirements of this Regulation and
carry out the necessary checks to ensure compliance of the pressure equipment with these requirements
.

Conclusions of the audit and the reasons shall notify the manufacturer.

5.4 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

5.5 The manufacturer shall inform the body which approved the quality
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in Section 5.2,
or whether a reassessment is necessary.


It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

6th Supervision notified body

6.1 The purpose of surveillance is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

6.2 For assessment purposes, allow the manufacturer to the notified body access to
locations of manufacture, inspection, testing and storage and provide
it with all necessary information, in particular

A) quality system documentation,

B) technical documentation as set out in Section 2

C) quality records, such as inspection reports, records of tests performed
records of calibrations performed, reports on the qualifications of the personnel
.

6.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer
report on the audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.

6.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
. The need and frequency of these additional visits will be determined on the basis
management system of inspection visits
used by the notified body.

This system must take into account the following factors:

A) category of device

B) the results of previous visits,

C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system is working properly
. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

7th CE marking and EU declaration of conformity

7.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 5.1 on each individual pressure equipment
which meets the relevant requirements of this Regulation.

7.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

8th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) the documentation specified in paragraph 5.1

B) the change referred to in paragraph 5.5, as approved and

C) the decisions, reports and reports from the notified body
set out in sections 5.3, 5.5, 6.3 and 6.4.

9th Each notified body shall inform the Authority for approval of a quality system
issued or withdrawn, and shall, periodically or upon request, make available a list of the Office
quality system, which it has refused, suspended or otherwise restricted
.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended or withdrawn, and
at the request of quality system approvals issued.

10th Authorised representative

Activities producers set out in paragraphs 3, 5.1, 5.5, 7 and 8 may be
his behalf and under his responsibility, by his authorized representative if
manufacturer in the commission authorized representative established.

9th CONFORMITY TO TYPE BASED ON VERIFICATION pressure equipment (MODULE F)

First Conformity to type based on verification of pressure equipment is part
conformity assessment procedure by which the manufacturer performs the activities set out in
points 2 and 5, and ensures and declares that the pressure
equipment that has been subjected to the provisions of paragraph 3 they are in conformity with the type
described in the EU type examination certificate and satisfy the requirements of this regulation
that apply to them.

Second Production

The manufacturer shall take all measures necessary so that the manufacturing process and its monitoring ensure compliance
manufactured pressure equipment is approved
type described in the EU type examination certificate and with the requirements of this regulation
that apply to them.

Third verification

Notified body, chosen by the manufacturer shall carry out appropriate
examinations and tests to check the conformity of pressure equipment
approved type described in the EU type examination certificate as
relevant requirements of this Regulation.

Examinations and tests to verify the conformity of the pressure equipment with the applicable requirements
be carried out by examination and testing of every product
set out in section 4.

Fourth Verification of conformity by examination and testing of each item of pressure equipment


4.1 All pressure equipment must be individually reviewed and carry out

Appropriate tests defined in the relevant harmonized standard
(harmonized standards), or equivalent tests, to check the conformity
pressure to the approved type described in the EU
type examination and the relevant requirements of this Regulation, which the
them. If this harmonized standard does not exist, decides
notified body concerned what the appropriate tests to be carried.

Notified body in particular:

A) verify that the personnel undertaking the permanent joining of pressure equipment
and non-destructive tests are qualified or
approved in accordance with sections 3.1.2 and 3.1.3 of Annex no. 1 to this
Regulation

B) verify the certificate issued by the material manufacturer in accordance with section 4.3 of Annex
no. 1 hereto and

C) shall carry out the final inspection and pressure testing
specified in paragraph 3.2 of Annex no. 1 hereto and possibly
examine the safety devices.

04.02 The notified body shall issue a certificate of conformity in respect to the examinations and tests
and each approved pressure equipment
procures or left on his own responsibility, affix its identification number
.

The manufacturer shall keep the certificates of conformity available for the supervisory authority for 10 years
by putting pressure on the market.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in Section 3 on each individual pressure equipment
is in conformity with the approved type described in the EU-type examination
satisfies the applicable requirements of this ordinance.

5.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority. If
with the notified body referred to in point 3 agrees, the manufacturer may provide
pressure equipment under the responsibility of the notified body also
identification number of that body.

6th If the notified body agrees, the manufacturer may, under the responsibility of the notified body
provide pressure equipment
identification number of that body during the manufacturing process.

7th Authorised representative

Activities manufacturer may be his behalf and under his responsibility
his authorized representative, if the manufacturer on behalf
authorized representative established.
Authorized representative is unable to perform the tasks set out in point 2.

10th CONFORMITY BASED ON UNIT VERIFICATION (MODULE G)

First Conformity based on unit verification is the procedure
conformity assessment procedure whereby the manufacturer performs the activities specified in paragraphs 2, 3 and 5
and ensures and declares that the pressure equipment
been subjected to the provisions of section 4 it is in conformity with the requirements of this regulation
which apply to it.

Second Technical documentation

The manufacturer shall establish the technical documentation and make it available to the notified
entity specified in section 4.

Documentation must enable the conformity of the pressure equipment with the relevant requirements
and include an adequate analysis and assessment
risk. The technical documentation shall specify the requirements and the extent
necessary for the assessment must cover the design, manufacture and operation
pressure equipment.

Technical documentation must include, if applicable, at least the following information
:

A) a general description of the pressure device

B) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

C) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

D) list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

E) results of design calculations, examinations carried out,

F) test and

G) the relevant information concerning the approval of manufacturing and testing procedures
and qualifications or approvals as required by
paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto.

Manufacturer keeps technical documentation at the disposal of the supervisory authority
over a period of 10 years from putting pressure on the market.

Third Production

The manufacturer shall take all measures necessary so that the manufacturing process and its

Monitoring ensure compliance of the pressure equipment with the relevant requirements of this Regulation
.

Fourth verification

Notified body, chosen by the manufacturer, perform or have performed
appropriate examinations and tests set out in the relevant harmonized standard
(harmonized standards), or equivalent tests to verify
conforms with the requirements of this ordinance.
If such a harmonized standard exists, decided by the notified body
what the appropriate tests to be carried out using other
technical specifications.

Particular the notified body

A) examine the technical documentation with respect to the design and manufacturing
procedures

B) assess the materials used where these are not in conformity with
relevant harmonized standards or with a European approval for
pressure equipment materials, and check the certificate issued
material manufacturer in accordance with section 4.3 of Annex no. 1 to this
regulation

C) approve the procedures for the permanent joining of
or check whether they have been previously approved in
accordance with paragraph 3.1.2 of Annex no. 1 hereto,

D) verify the qualifications or approvals required under
requirements set out in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto and

E) carry out the final inspection specified in paragraph 3.2.1 of Annex no. 1 to
this Regulation shall carry out a pressure test
set out in clause 3.2.2 of Annex no. 1 hereto, and possibly examine
safety equipment.

Notified body shall issue a certificate of conformity in respect to the examinations and tests
and approved pressure equipment affix or let
own responsibility, affix its identification number. Manufacturer
holds certificates of conformity at the supervisory authority for 10 years since
putting pressure on the market.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 4 on each individual pressure equipment
meets the relevant requirements of this Regulation.

5.2 The manufacturer shall draw up a written EU declaration of conformity for 10 years from
placing pressure equipment on the market shall make available to the supervisory authority
. The EU declaration of conformity indicated pressure equipment for which
been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

6th Authorised representative

Activities producers set out in paragraphs 2 and 5 may be his name and on his
responsibility, by his authorized representative, if the manufacturer
in the commission authorized representative established.

11th CONFORMITY BASED ON FULL QUALITY ASSURANCE (MODULE H)

First Conformity based on full quality assurance is the procedure
conformity assessment procedure whereby the manufacturer performs the activities specified in paragraphs 2 and 5
ensures and declares that the pressure equipment
meet the requirements of this Regulation which apply to them .

Second Production

The manufacturer shall operate an approved quality system for design, production,
final product inspection and testing of the pressure device according to claim 3
subject to supervision under Section 4

Third Quality system

3.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include:

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) the technical documentation for one model of each type of pressure
device to be produced; Technical documentation must contain
if applicable, at least the following information:

I) a general description of the pressure device

Ii) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

Iii) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

Iv) a list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

V) results of design calculations, examinations carried out,

Vi) test reports,

Vii) the documentation concerning the quality system and

Viii) a written declaration that the same application has not been lodged with any other notified body
.

3.2 The quality system must ensure compliance of the pressure equipment with
requirements of this Regulation which apply to them.

All the elements, requirements and provisions adopted by the manufacturer must be

Documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description

A) objectives in terms of quality and organizational structure, responsibilities and powers of the management
terms of design quality and product

B) technical design specifications, including standards that will be applied and
in the event that the relevant harmonized standards apply throughout
extent, the means that will be used to ensure the fulfillment
essential requirements of this regulation, which is at a given pressure
equipment relate

C) the inspection and design verification techniques, processes and systematic
actions that will be used when designing the pressure equipment
belonging to the type of pressure equipment, particularly with regard to
materials in accordance with section 4 of Annex no. 1 hereto,

D) appropriate methods, processes and systematic actions that
used in manufacturing, quality control and quality assurance, particularly
operating procedures used for the joining of parts,
approved in accordance with paragraph 3.1.2 Annex no. 1 hereto,

E) examination and tests that will be carried out before, during
and after manufacture, the frequency with,

F) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications or approvals of the workers, especially workers who perform
joining of parts and
destructive tests specified in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 hereto and

G) the means of supervising the achievement of the required design and quality
pressure equipment and the effective operation of the system
quality.

3.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 3.2. The elements of the quality system by
corresponding specifications relevant harmonized standards
compliance with these requirements.

The assessment team must have experience in quality management systems and
least one member must have experience of assessments of the technology
pressure equipment and knowledge of the applicable requirements of this Regulation.
Audit includes an assessment visit to the manufacturer's premises.

Audit team to examine the technical documentation specified in paragraph 3.1
point. b) to verify the manufacturer's ability to identify the relevant requirements of this Regulation
and carry out the necessary checks to ensure compliance
pressure equipment with these requirements.

Shall notify the manufacturer or his authorized representative
audit findings and the reasons given.

3.4 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

3.5 The manufacturer shall inform the body which approved the quality system
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in paragraph 3.2,
or whether a reassessment is necessary.

It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

Fourth Supervision notified body

4.1 The purpose of supervision is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

4.2 For assessment purposes, allow the manufacturer to the notified body access to
the design, manufacture, inspection, testing and storage
and provide it with all necessary information, in particular:

A) quality system documentation,

B) the quality records required under the quality system for the design of
, such as results of analyzes, calculations, tests and

C) the quality records required in the manufacturing part of the quality system
such as inspection reports, records of tests carried out
records of calibrations performed, reports on the qualifications of the personnel
.

4.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer
report on the audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.

4.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
.

Need and frequency of these additional visits will be determined on the basis
management system audit visits used by the notified body.
This system must take into account the following factors:

A) category of device

B) the results of previous visits,


C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system is working properly
. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

Fifth CE marking and EU declaration of conformity

5.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 3.1 on each individual pressure equipment
which meets the relevant requirements of this Regulation.

5.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 from putting pressure on the market is
shall make available to the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

6th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) technical documentation as set out in paragraph 3.1

B) the documentation concerning the quality system as set out in paragraph 3.1

C) change information set out in paragraph 3.4, as approved and

D) decisions, reports and reports from the notified body
set out in paragraphs 3.3, 3.4, 4.3 and 4.4.

7th Each notified body shall inform the Authority for approval of a quality system
issued or withdrawn, and shall, periodically or upon request, make available a list of the Office
quality system, which it has refused, suspended or otherwise restricted
.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended or withdrawn, and
at the request of quality system approvals issued.

8th Authorised representative

Activities producers set out in paragraphs 3.1, 3.5, 5 and 6 may be
his behalf and under his responsibility, by his authorized representative if
manufacturer in the commission authorized representative established.

12th CONFORMITY BASED ON FULL QUALITY ASSURANCE WITH DESIGN reviewing
(module H1)

First Conformity based on full quality assurance with design examination
and special surveillance of the final assessment is the conformity assessment procedure
whereby the manufacturer performs the activities specified in paragraphs 2 and 6
ensures and declares that the pressure equipment meet
requirements of this Regulation which apply to them.

Second Production

The manufacturer shall operate an approved quality system for design, production,
final product inspection and testing of the pressure equipment provided for in Section 3
and subject to the supervision provided for in paragraph 5. The suitability of the technical design
pressure equipment must be examined under Section 4.

Third Quality system

3.1 manufacturer with a notified body of his choice for the
assessment of his quality system for the pressure equipment.

The application must include:

) The name and address of the manufacturer and, if the application is lodged by the authorized representative,
his name and address

B) the technical documentation for one model of each type of pressure
device to be produced; Technical documentation must contain
if applicable, at least the following information:

I) a general description of the pressure device

Ii) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

Iii) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment

Iv) a list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

V) results of design calculations, examinations carried out,

Vi) test reports,

Vii) the documentation concerning the quality system and

Viii) a written declaration that the same application has not been lodged with any other notified body
.

3.2 The quality system must ensure compliance of the pressure equipment with
requirements of this Regulation which apply to them.

All the elements, requirements and provisions adopted by the manufacturer must be
documented systematic and orderly manner in the form of written policies, procedures and instructions
. Quality system documentation must permit uniform interpretation
programs, plans, manuals and records relating to quality.

Quality system documentation must contain in particular an adequate description of:

A) objectives in terms of quality and organizational structure, responsibilities and

Powers of the management in terms of quality of design and product

B) technical design specifications, including standards that will be applied and
in the event that the relevant harmonized standards apply throughout
extent, the means that will be used to ensure the fulfillment
essential safety requirements of this Regulation
that the pressure equipment,

C) the inspection and design verification techniques, processes and systematic
actions that will be used when designing the pressure equipment
belonging to the type of pressure equipment, particularly with regard to
materials in accordance with section 4 of Annex no. 1 hereto,

D) appropriate methods, processes and systematic actions that
used in manufacturing, quality control and quality assurance, particularly
operating procedures used for the joining of parts,
approved in accordance with paragraph 3.1.2 Annex no. 1 hereto,

E) examination and tests that will be carried out before, during
and after manufacture, the frequency with,

F) quality records, such as inspection reports, records of tests performed
, records of calibrations, reports
qualifications or approvals of the personnel, especially those
workers who perform the joining of parts
and non-destructive tests specified in paragraphs 3.1.2 and 3.1.3 of Annex no. 1 to this Order and


G) the means of supervising the achievement of the required design and quality
pressure equipment and the effective operation of the system
quality.

3.3 The notified body must assess the quality system to determine whether it satisfies
requirements set out in 3.2.

The elements of the quality system that comply with the corresponding specifications
relevant harmonized standards, compliance with these requirements.
The assessment team must have experience in quality management systems and
least one member must have experience of evaluation in the relevant
pressure equipment and the assessment of pressure equipment technology concerned
and knowledge of the applicable requirements of this Regulation.
The audit includes an assessment visit to the manufacturer's premises.

Audit team to examine the technical documentation specified in paragraph 3.1
point. b) to verify the manufacturer's ability to identify the relevant requirements of this Regulation
and carry out the necessary checks to ensure compliance
pressure equipment with these requirements.

Shall notify the manufacturer or his authorized representative
audit findings and the reasons given.

3.4 The manufacturer must undertake to fulfill the obligations arising from
approved quality system and to maintain it so that it remains adequate and efficient
.

3.5 The manufacturer shall inform the body which approved the quality system
of any intended change of the quality system.

Notified body shall evaluate the proposed changes and decide whether the modified
quality system will continue to satisfy the requirements set out in paragraph 3.2,
or whether a reassessment is necessary.

It must notify the manufacturer of its decision.
Notification must contain the conclusions of the examination and the reasoned assessment decision.

3.6 Each notified body shall inform the Office system approvals
quality issued or withdrawn, and shall, periodically or upon request, make available
Office list of quality system approvals refused,
suspended or otherwise restricted.

Each notified body shall inform the other notified bodies
quality system approvals refused, suspended or withdrawn, and
at the request of quality system approvals issued.

Fourth Design review

4.1 The manufacturer must lodge an application for examination of the design of each pressure
device in which the notified body referred to in paragraph 3.1 has not
design review earlier.

4.2 The application must enable the design, manufacture and operation
pressure equipment and shall enable conformity with the requirements of this regulation
which apply to it. The application must include:

) The name and address of the manufacturer

B) a written declaration that the same application has not been lodged with another
notified body

C) technical documentation. The documentation must allow assessment of the conformity
pressure equipment with the requirements and provides adequate
analysis and risk assessment. The technical documentation shall mention
requirements and to the extent necessary for the assessment must cover the design and operation of the pressure device
. The technical documentation must contain
if applicable, at least the following information:

I) a general description of the pressure device

Ii) conceptual design and manufacturing drawings and diagrams of components, sub-assemblies,
circuits

Iii) descriptions and explanations necessary for the understanding of those drawings and diagrams and the operation
pressure equipment


Iv) a list of harmonized standards which have been published in the Official Journal
European Union, which were used in their entirety
or in part, and descriptions of the solutions adopted to meet the safety requirements
thereof,
where those harmonized standards have not been applied; in the case of partly applied harmonized
standards, the technical documentation shall specify the parts which have been used

V) results of design calculations, examinations carried out,

Vi) test reports and

Vii) supporting evidence for the adequacy of the technical design.
This supporting evidence shall mention any documents that have been applied, in particular
where the relevant harmonized standards have not been applied in full, and the
if necessary, include the results of tests carried out by the appropriate laboratory of the manufacturer or
another testing laboratory on his behalf and on his
responsibility.

4.3 The notified body shall examine the application and where the design meets the requirements of this Regulation
that the pressure equipment, manufacturers shall
EU design examination certificate.
The certificate must contain the name and address of the manufacturer, conclusions of the examination
validity and the necessary data for identification of the approved design.

The certificate may be accompanied by one or more attachments.

Certificate and its annexes shall contain all relevant information enabling
assess whether products manufactured in conformity with
examined design, and possibly to check for traffic.

If the proposal does not meet the relevant requirements of this Regulation, the notified body refuses to issue
design examination certificate and shall inform the applicant
, with detailed reasons for the rejection.

4.4 The notified body shall to be informed of any changes
generally acknowledged state of the art, which would indicate that
approved design may no longer comply with the applicable requirements of this Regulation and decide
whether such changes require additional investigation. If
investigation, the notified body shall inform the manufacturer.

The manufacturer shall inform the body which issued the EU design examination
of all modifications to the approved design that may affect
conformity with the essential safety requirements of this Regulation
or on the conditions of its validity. These changes must be notified
body that issued the EU design examination certificate, additionally
form of an addition to the original EU design examination certificate.

4.5 Each notified body shall inform the Authority of certificates
EU design examination or any additions thereto which it has issued or withdrawn, and
periodically or upon request, make available a list of the Office
certificates or additions thereto refused, suspended or otherwise restricted.

Each notified body shall inform other notified bodies of
EU design examination certificates and additions thereto refused,
suspended or otherwise restricted, and, on request, of the certificates or
additions thereto which it has issued .

European Commission, EU Member States and the other notified bodies
notified body may ask for a copy of the certificate examination
EU draft or amendments thereto. The European Commission and the Member States of the European Union
may request a notified body a copy of the technical documentation and
results of the examination conducted by him.

The expiry of the EU design examination certificate, the notified body keeps
copy of this certificate, its annexes and additions, as well
technical file including the documentation submitted by the manufacturer.

4.6 The manufacturer shall make available to the supervisory authority
copy of the EU design examination, its annexes and additions together with the technical
documentation for a period of 10 years from putting pressure on the market.

Fifth Supervision notified body

5.1 The purpose of surveillance is to ensure that the manufacturer duly fulfills the obligations
arising from the approved quality system.

5.2 For assessment purposes, allow the manufacturer to the notified body access to
the design, manufacture, inspection, testing and storage
and provide it with all necessary information, especially

A) quality system documentation,

B) the quality records required under the quality system for the design of
, such as results of analyzes, calculations, tests and

C) the quality records required in the manufacturing part of the quality system
such as inspection reports, records of tests carried out
records of calibrations performed, reports on the qualifications of the personnel
.

5.3 The notified body shall conduct periodic audits to make sure that
manufacturer maintains and applies the quality system and provide the manufacturer
report on the audit. The frequency of periodic audits must be such that every three years
was an overall reassessment.


5.4 Additionally, the notified body may pay the manufacturer unannounced inspection visits
.

Need and frequency of these additional visits will be determined on the basis
management system audit visits used by the notified body.
This system must take into account the following factors:

A) category of device

B) the results of previous visits,

C) the need to monitor remedial measures

D) any special conditions linked to the approval system and

E) significant changes in manufacturing organization, policy or techniques.

During such visits the notified body may carry out
or have carried out product testing to verify that the quality system is working properly
. Shall provide the manufacturer with a visit report and protocol
test if the tests were performed.

5.5 Special surveillance of the final assessment

Final assessment as set out in paragraph 3.2 of Annex no. 1 hereto
subject to increased surveillance in the form of unannounced inspection visits
by the notified body. During these visits, the notified body carries out an examination
pressure equipment.

Shall provide the manufacturer with a visit report and protocol of
tests if the tests were performed.

6th CE marking and EU declaration of conformity

6.1 The manufacturer shall affix the CE marking and identification number of the notified
entity specified in paragraph 3.1 on each individual pressure equipment
which meets the requirements of this Regulation.

6.2 The manufacturer shall establish, for each model of the pressure device
written EU declaration of conformity for 10 years from putting pressure equipment on the market
is kept at the disposal of the supervisory authority. The EU declaration of conformity is given
model of pressure equipment which has been drawn up, and also
number of the design examination certificate.

Copy of the EU declaration of conformity upon request, to the supervisory authority.

7th The manufacturer shall make available to the supervisory authority for 10 years since the
pressure equipment on the market

A) the documentation concerning the quality system as set out in paragraph 3.1

B) the change referred to in paragraph 3.5, as approved and

C) the decisions, reports and reports from the notified body
set out in paragraphs 3.5, 5.3 and 5.4.

8th Authorised representative

Manufacturer's authorized representative may, on behalf of the manufacturer and responsibility
submit an application as set out in sections 4.1 and 4.2 and carry out the tasks set
in paragraphs 3.1, 3.5, 4.4, 4.6, 6 and 7, if the manufacturer in commission
authorized representative established.
Appendix 4


EU declaration of conformity (no. XXXX) ^ 8)

First Pressure equipment or assembly (article number, type or production
batch or serial number):

Second Name and address of the manufacturer and of his authorized representative:

Third This declaration of conformity is issued under the sole responsibility of the manufacturer.

Fourth Object of the declaration (identification of the pressure equipment or assemblies
enabling them to be traced back; if it is for identification purposes
pressure equipment or assembly required, can include images)

A) description of the pressure equipment or assemblies

B) the conformity assessment procedures or

C) in the case of assemblies, description of the pressure equipment constituting the assembly and
conformity assessment procedures utilized.

Fifth The above described object of the declaration is in conformity with the relevant
harmonization legislation of the European Union:

6th References to the relevant harmonized standards used, or
other technical specifications under which conformity is declared:

7th Alternatively, the name, address and number of the notified body which carried
conformity assessment and issued certificate number and a link to the certificate
EU production type examination certificate examination EU-type design
, EU design examination certificate or certificate of conformity.

8th Further information:

Signed for and on behalf of:

(Place and date of issue)

(Name, function) (signature)

(Or the identification of the person who is authorized to sign a legally binding
declaration for the manufacturer or his authorized representative)

1) Directive of the European Parliament and Council Directive 2014/68 / EU of 15 May
2014 on the harmonization of the laws of the Member States concerning
supply pressure on the market.

2) Decree no. 119/2016 Coll., On Conformity Assessment
simple pressure vessels when made available on the market.

3) Decree no. 194/2001 Coll., Laying down technical
requirements for aerosol dispensers, as amended.

4) Act no. 56/2001 Coll., On conditions for operating vehicles on roads
roads and amending Act no. 168/1999 Coll., On liability insurance for damage caused
operation of a vehicle and amending some related
acts (vehicle insurance), as amended

Act no. 307/1999 Coll., As amended.

Decree no. 341/2014 Coll., On approval of roadworthiness and
technical conditions for operating vehicles on roads.

5) European Parliament and Council Regulation (EU) no. 167/2013 of 5 February 2013
the approval of agricultural and forestry vehicles and surveillance
market for these vehicles.

Regulation of the European Parliament and Council Regulation (EU) no. 168/2013 of 15 January 2013
approval of two- or three-wheelers and four-wheelers and
market surveillance of these vehicles.

6) Decree no. 22/2003 Coll., Laying down technical requirements
on appliances burning gaseous fuels.

Decree no. 176/2008 Coll., On technical requirements for machinery
equipment, as amended.

Decree no. 54/2015 Coll., On technical requirements for medical devices
.

Decree no. 122/2016 Coll., On conformity assessment of lifts and their safety components
.

Decree no. 116/2016 Coll., On Conformity Assessment
equipment and protective systems intended for use in potentially explosive atmospheres
when made available on the market.

Decree no. 118/2016 Coll., On Conformity Assessment
electrical equipment designed for use within certain voltage limits in their
available on the market.

7) Act no. 114/1995 Coll., On Inland Navigation, as amended
regulations.

Decree no. 208/2011 Coll., On technical requirements for
transportable pressure equipment.

Annex no. I to Decree no. 8/1985 Coll., On the Convention on International
Carriage by Rail (COTIF), as amended.

Decree no. 64/1987 Coll., On European Agreement on International Road
Carriage of Dangerous Goods (ADR), as amended.

Convention no. 147/1947 Coll., On international civil aviation, as amended
.

8) The manufacturer may allocate a declaration of conformity number.