122/2016 Sb.



GOVERNMENT REGULATION



of 30 March 2004. March 2016



on the assessment of the conformity of lifts and their safety components



The Government directs pursuant to § 4 and § 50 para. 5 of law No. 90/2016 Coll.

conformity assessment of specified products when they are making available on the market (hereinafter

"the Act"):



§ 1



The subject of the edit



(1) this regulation incorporates the relevant provision of the European Union ^ 1) and

regulates the technical requirements for lifts and safety components for

lifts must comply when placing on the market and/or put into service,

the conditions and procedures for the supply of safety components for lifts on

the market and the conformity assessment methods.



(2) this Regulation shall apply to lifts permanently serving buildings

or construction and are designed for the transport



) of the person,



(b) persons and goods), or



c) goods alone if the carrier is accessible, you can to it without difficulty

to enter and is equipped with a control device on the carrier or within reach of

a person who is located on it.



(3) this Regulation shall also apply to safety components for

lifts listed in annex 3 to this regulation, which are designed for

the use of lifts as referred to in paragraph 2.



(4) this Regulation shall not apply to



and) lifting equipment, whose design speed does not exceed 0.15

m/s,



b) construction site hoists,



c) cableway installations, including funicular railways,



d) lifts specially designed and constructed for military or police

purposes,



e) lifting appliances from which work can be carried out,



f) mining equipment



g) lifting appliances intended for lifting performers

during the performance,



h) lifting devices in vehicles



I) lifting appliances connected to machinery and intended exclusively for

access to workstations including maintenance and inspection on

the machinery,



j) COG railways and



k) escalators and moving walkways.



(5) in cases where the risks associated with lifts or safety

components for lifts is used in this regulation are wholly or

partially covered in another law or directly

the applicable legislation of the European Union, this regulation on these lifts

or safety components for lifts and such risks shall not apply.



§ 2



Definition of terms



For the purposes of this regulation, means a



and) the carrier part of the lift by which persons may be present or cargo

for the purpose of lifting or lowering,



(b) the representative model of the lift) lift whose technical dossier

shows the way how they met the basic requirements for the protection of the health and

safety requirements set out in annex 1 to this regulation, for lifts

derived from the model lift defined by objective

parameters, which uses identical safety components for lifts



(c)) is a technical specification document that prescribes technical

the requirements, which has a lift or safety component for lifts

meet the.



§ 3



Technical requirements for lifts and safety components for lifts



Basic technical requirements for lifts and safety components

for lifts are basic requirements for health and safety

set out in annex 1 to this regulation, which the

proves conformity assessment. Safety components for lifts must

to meet these requirements, the lifts in which they are

incorporated.



§ 4



Making available on the market and putting into service



(1) the elevators can be placed on the market and put into service only if the

are installed correctly, and provided that they are maintained and

used for their intended purpose and comply with the requirements laid down in this

by regulation.



(2) safety components for lifts can be supplied on the market and

put into service only if, when, under the assumption that they will be

properly built, maintained and used for its intended purpose, satisfy the

the requirements laid down in this regulation.



(3) For trade fairs, exhibitions and demonstrations can perform elevators or

safety components for lifts that are not in compliance with this

by regulation, if a visible sign clearly that these elevators and

components are not in conformity, and shall not be placed or made available on the market,

until brought into conformity. When their demonstrations must be made

security measures to ensure the safety of persons.



§ 5



The manufacturer of the



(1) the manufacturer when placing safety components for lifts on the market

shall ensure that these safety components for lifts were designed and

manufactured in accordance with § 3, it shall draw up the required technical documentation

and carry out or have carried out the conformity assessment procedure

as set out in section 10.



(2) if the conformity of the safety components for lifts with established

the essential requirements, conformity assessment procedure proved, shall draw up

EU Declaration of conformity, the manufacturer shall ensure that the safety

component for lifts is accompanied by, and positioned according to § 14 of the CE marking.



(3) the manufacturer shall keep the technical documentation referred to in annex 4 to

This regulation and the EU Declaration of conformity and, where appropriate, the decision on the

the approval for a period of 10 years after the safety components for lifts

on the market.



(4) the manufacturer shall carry out in order to protect consumer health and safety

sample testing of safety components for lifts that came on the market and

the necessary investigation, if this is necessary due to the risks

is a security component for lifts. These tests and investigations

shall be carried out to the extent necessary to confirm or rebut the

of the risks involved. Producer keeps a register of complaints, of non-conforming

safety components for lifts and safety components download

for lifts from the circulation of these activities on an ongoing basis and shall inform the

distributors and vendors.



(5) the manufacturer shall ensure that the safety component for lifts

you stated on the market bear a type, batch or serial number or

or other element allowing their identification, or, where the

the size or nature of the safety components for lifts do not allow

the required information is listed on a label inseparably attached to the

safety component for lifts.



(6) the manufacturer shall indicate in a safety component for lifts, or, if not

possible, on a label inseparably attached to the safety component

for lifts in your name or business name or trade mark, and

address for service, at which he can be contacted. Address for

delivery address must be the place in which the manufacturer can be truly

to reach you. Contact details are given in a language easily understood by the

to end users and to the supervisory authority.



(7) the manufacturer shall ensure that the safety component for lifts

accompanied by the instructions referred to in point 6.1 of annex 1 to this regulation in the Czech

language. This manual and any markings on the safety

the component is placed, must be clear, comprehensible and easily

to understand.



§ 6



Authorized representative



(1) the authorized representative appointed pursuant to § 29 para. 3 of the Act shall not be

the vendor commissioned to fulfil any of the obligations specified in § 29 para.

1 (b). and even to) Act, the obligation to draw up the technical documentation

According to § 29 para. 1 (b). (b)) of the Act, however, must allow him credentials

keep the EU Declaration of conformity or keep a document about

approval of the quality system of the supplier and technical documentation and

allow him to provide synergy to the supervisory authorities.



(2) the authorized representative shall keep the EU Declaration of conformity and, where appropriate,

the document of approval of the quality system of the manufacturer or supplier, and

the technical documentation for the requirements of a supervisory authority for a period of 10 years from the

placing safety components for lifts or lift on the market.



§ 7



The importer



(1) the importer before placing safety components for lifts on the market

shall ensure that the manufacturer has made one of the conformity assessment procedures referred to in §

10, has drawn up the technical documentation, that the safety component for

lifts bear the CE marking, to be accompanied by an EU Declaration of conformity

and the required documents and that the manufacturer has complied with the requirements set out in section 5 of the

paragraph. 5 and 6.



(2) the importer shall indicate on the safety component for lifts, or, if not

possible, on its packaging or in a document attached to the safety component

your name or business name or trade mark and the address for

service, at which he can be contacted. Contact details are given in the

language easily understood by end users and to the supervisory authority.



(3) the importer shall ensure that the safety component for lifts

accompanied by the instructions referred to in point 6.1 of annex 1 to this regulation in the Czech

language.



(4) the importer performs in order to protect consumer health and safety

sample testing of safety components for lifts and the necessary investigation,

If it is appropriate to the risks, which is a security

component for lifts. These tests and the investigation is carried out to the extent

required for confirmation or refutation of the risks involved. The importer

a register of complaints, non-conforming leads safety components for

lifts and safety components for lifts the withdrawal from circulation and to keep

about these inspection activities shall inform distributors.




(5) the importer for a period of 10 years after the safety components for

lifts on the market keeps a copy of EU Declaration of conformity and, where appropriate,

decision on the approval of the supervisory authority and ensures that this

authority may be submitted technical documentation on request.



§ 8



Distributor



The distributor prior to delivery of the safety components for lifts on the market

verifies whether the



a) safety component for lifts bears the CE marking, the



(b)) is a safety component for lifts is accompanied by the EU Declaration of

conformity, the required documents and instructions referred to in point 6.1 of Appendix No. 1 to this

Regulation in the Czech language and



(c)) that the manufacturer and the importer have met the applicable requirements set out in section 5 of the

paragraph. 5 and 6 and § 7 (2). 2.



§ 9



Time to identify the operator



Economic operator for a period of 10 years from the delivery of the safety component

for lifts, keeps the data that can be used at the request of the supervisory authority

specify the operator that his safety component for lifts

He added, or to whom a safety component for elevators, he added.



§ 10



The conformity assessment procedures for safety components for lifts



Safety components for lifts must be subjected to one of

the following conformity assessment procedures:



and) type safety components for lifts shall be subjected to examination of the EU

type (module B) as laid down in part A of annex 4 to this regulation and

conformity to type is the procedure ensures conformity to type with random checking

selection, in terms of safety components for lifts (module C2),

in accordance with Annex 9 to this regulation,



b) type safety components for lifts shall be subjected to examination of the EU

type (module B) as laid down in part A of annex 4 to this regulation and

conformity to type is the procedure ensures conformity to type based on the

quality assurance of the products with regard to safety component for

lifts (module E) referred to in annex 6 to this regulation,



c) conformity assessment based on full quality assurance (module H)

According to annex 7 to this regulation.



§ 11



The conformity assessment procedures for lifts



(1) the lifts must be subjected to one of the following procedures

conformity assessment:



and) if it is designed and manufactured according to the model lift, which was

subjected to the EU type-examination (module B) as described in part B of the annex No 4 to

of this regulation, shall be subject to



1. final inspection of the lift in accordance with annex 5 to this regulation,



2. conformity to type based on quality assurance of the products in terms of

lifts (module E) referred to in annex 10 to this regulation, or



3. conformity to type based on quality assurance of the production, as regards

lifts (module D) referred to in annex 12 to this regulation, or



(b)) if they have been designed and manufactured according to the approved quality system

(module H1) as defined in annex 11 to this regulation, shall be

subjected to



1. final inspection of the lift in accordance with annex 5 to this regulation,



2. conformity to type based on quality assurance of the products in terms of

lifts (module E) referred to in annex 10 to this regulation, or



3. conformity to type based on quality assurance of the production, as regards

lifts (module G) referred to in annex 12 to this regulation, or



c) conformity based on unit verification when it comes

of lifts (module E) referred to in annex 8 to this regulation, or



d) conformity based on full quality assurance plus design examination

as for lifts (module H1), as defined in annex 11 to this regulation.



(2) in the cases referred to in paragraph 1 (b). a) and (b)), if the person

to ensure the design and manufacture of the elevator is not identical to the person responsible for the

install and test the lift, it gives the person responsible for the design and manufacture of

lift the person responsible for the installation and test an elevator available

all the necessary documents and information, to the person responsible for

install and try out the elevator to ensure correct and safe installation and

try out the elevator.



(3) any permitted differences between the lift and the lifts derived

from the model lift must be clearly specified in the technical

documentation (with maximum and minimum values).



(4) the similarity of the type series devices can be demonstrated by calculation or

structural drawings to demonstrate how compliance with the essential

technical requirements.



§ 12



Presumption of conformity



If the lift or safety component for lifts in conformity with

harmonised standards, the references of which have been published in the official

Journal of the European Union, or parts thereof, it shall be deemed to be in

the basic technical requirements to which those standards or

parts thereof.



section 13 of the



EU Declaration of conformity



(1) the EU Declaration of conformity to meet basic technical

requirements.



(2) the EU Declaration of conformity shall be drawn up in accordance with the model set out in

Annex 2 to this regulation. The statement contains the information set out in

some of the attachments size 5 to 12, to this regulation and must still be

updated. EU Declaration of conformity is also translated into the language or

languages required by the Member State of the European Union, in which the lift or

safety component for lifts placed or made available on the market.



(3) where the lift or safety component for lifts by

more harmonisation of European Union providing for the development of the EU

the Declaration of conformity be drawn up a single EU Declaration of conformity with the

links to all of these rules according to which it was considered a match,

including links to their publication. This single EU Declaration of conformity

may take the form of a folder consisting of declarations of conformity issued by the

each of the regulations.



§ 14



The CE marking and other markings



(1) the CE marking before placing on the market shall affix to each elevator cage

and on each security component for lifts, or if it is not

possible, on a label inseparably attached to the safety component for

elevators.



(2) the CE marking on the lift connects the identification number of the notified

the operator who participated in the assessment of the conformity of the lift in accordance with one of the

the following procedures, which are:



and) final inspection in accordance with annex 5 to this regulation,



b) the unit verification (module G) referred to in annex No. 8

to this regulation,



(c)), quality assurance (H1 or modules E, D) as defined in annexes 10, 11

or 12 of this regulation.



(3) the identification number referred to in paragraph 2 connects itself to the notified

body, or as directed by the supplier or his authorised

representative.



(4) the CE marking on the safety component for lifts connects

the identification number of the notified body involved in the assessment

the conformity of the safety components for lifts under any of the

the following procedures, which are:



product quality assurance) (module E) referred to in annex 6 to this

Regulation,



(b)) the full quality assurance (module H) referred to in annex 7 to this

Regulation,



(c)) to check conformity to type with random sampling, with regard to security

components for lifts (module C2), in accordance with Annex 9 to this regulation.



(5) the identification number referred to in paragraph 4 connects itself to the notified

body, or as directed by the manufacturer, or his authorised

representative.



(6) the CE marking, or the identification number of the notified

the body may be followed by any other mark indicating a special

risk or use.



§ 15



Formal defects



A formal deficiency is considered when



and) the CE marking was placed in breach of article. 30 of the regulation of the European

Parliament and of the Council (EC) no 765/2008 of 9 June. July 2008 laying

sets out the requirements for accreditation and market surveillance relating to the marketing of

products on the market and repealing Regulation (EEC) No 339/93, or with section

14. 1,



(b)) the CE marking has not been affixed,



(c) the identification number of the notified body) were placed in violation of §

14 or in violation of § 14 has not been located,



d) EU Declaration of conformity has not been drawn up,



e) EU Declaration of conformity has not been drawn up in accordance with this

by regulation,



f) technical documentation referred to in parts A and B of the annex No 4 to this

in the annexes to Regulation No 7, 8 and 11 of this regulation is missing or

incomplete,



(g)) the name or business name, trademark, or, where appropriate, address

for service manufacturer, supplier or importer has not been listed in the

accordance with § 29 para. 1 (b). g) of the Act, § 5 para. 6 or § 7 para. 2,



h) information allowing identification of the lift or the safety

components for lifts have not been given in accordance with § 29 para. 1 (b). (f))

the Act or § 5 para. 5, or



I) to the lift or safety component for lifts is not accompanied by

the guides referred to in § 29 para. 1 (b). h) of the Act or § 5 para. 7 or

These tutorials are not in accordance with the relevant requirements.



section 16 of the



Transitional provisions



(1) Lifts complying with requirements of Government Regulation No. 27/2003 Coll., as amended by

effective before the date of entry into force of this regulation, may continue to be

put into service if they have been placed on the market before the date of the acquisition of

the effectiveness of this regulation.



(2) safety components for lifts complying with the requirements of regulation

No. 27/2003 Coll., in the version in force before the date of entry into force of


of this regulation, may continue to be placed on the market if they have been listed

on the market before the date of entry into force of this regulation.



(3) the valid certificates and other documents certifying the detected

fact released persons notified pursuant to Decree-Law No.

27/2003 Coll., in the version in force before the date of entry into force of this

Regulation, shall remain in force and shall be deemed the certificates and other

the documents certifying the facts established under this regulation.



§ 17



Regulation (EEC)



Shall be deleted:



1. Government Regulation No. 27/2003 Coll. laying down technical requirements

on the lifts.



2. Government Regulation No. 127/2004 Coll., amending Decree-Law No.

27/2003 Coll. laying down technical requirements for elevators.



3. Government Regulation No. 142/2008 Coll., amending Decree-Law No.

27/2003 Coll. laying down technical requirements for lifts, as amended by

Government Regulation No. 127/2004 Coll.



section 18



The effectiveness of the



This Regulation shall enter into force on 20 March 2004. April 2016.



Prime Minister:



Mgr. Sobotka in r.



Minister of industry and trade:



Ing. Mládek, CSc., r.



Č. 1



THE BASIC REQUIREMENTS FOR HEALTH AND SAFETY



INTRODUCTORY PROVISIONS



1. the obligations relating to the essential requirements for the protection of the health and

safety shall apply only if the lift or

safety components for lifts, when used in accordance with the conditions

the vendor or manufacturer of the risk.



2. Basic requirements for health and safety, which are

contained in this regulation, are binding. Goals that set out, however,

in the current state may not be attainable. In these cases,

must be a lift or safety components for lifts designed and

constructed in such a way as to come closer to these as much as possible

objectives.



3. the supplier shall carry out a risk assessment to identify all

risks relating to lift or safety components for lifts

they produced; These products must then design and construct with regard to

This analysis.



1. In general



1.1 the use of the Government Regulation No. 176/2008 Coll. on technical requirements

to machinery, as amended (hereinafter referred to as "regulation

No 176/2008 Sb. ").



If there is a relevant risk that is not listed in this annex,

applies the basic requirements for health and safety related

design and construction of machinery referred to in annex 1 to the

Government Regulation No. 176/2008 Coll., the essential requirements for the protection of the health and

the security referred to in point 1.1.2 of annex 1 to the Decree-Law No.

176/2008 Coll. shall apply in every case.



1.2 carrier



The carrier shall take the form of the lift cage. This car must be

designed and constructed in such a way that its space and strength match

the supplier designated by the maximum number of persons and the load capacity of the lift.



If dimensions permit, the car must be the lift is intended for

the transport of people designed and constructed so that its construction

features do not obstruct or impede access and use to persons with limited

mobility and to allow any appropriate adjustments,

that may facilitate its use to such persons.



1.3 suspension and means equipment



Hanging or supporting devices the car, its attachments and

connecting parts must be selected and designed so as to provide

the necessary level of safety and to minimize the risk of the car falling,

taking into account the conditions of use, the materials used and

production conditions.



Where to hang the cages, ropes or chains must be used

at least 2 separate ropes or chains, each with its own

fastening. The ropes and chains must not have any joins or splices except,

If it is not necessary for fixing or to create an ok.



1.4. control of loading (including overspeed)



1.4.1. Lifts must be so designed, constructed and installed so that in the

case of exceeding carrying capacity has been prevented from command to be put into motion.



1.4.2. Lifts must be equipped with a speed limitation device.



This requirement does not apply to lifts in which the design of the actuator

prevents exceeding the speed limit.



1.4.3. Fast lifts must be equipped with a device controlling and

the limiting speed.



1.4.4. Lifts driven by friction pulleys must be designed so that

ensure the stability of the traction cables on the pulley.



1.5 lift machinery



1.5.1 all passenger lifts must have their own individual lift machinery. This

requirement does not apply to lifts in which the balance weight

replaced the second cage.



1.5.2. the Contractor shall ensure that the lift machinery and the associated devices

are not accessible except for maintenance and in emergencies.



1.6 Control



1.6.1. the controls of lifts intended for persons with reduced mobility

motion and orientation must be suitably constructed and fitted.



1.6.2. the function of the controls must be clearly marked.



1.6.3 the call circuits of a group of lifts may be shared or

linked.



1.6.4. Electrical equipment must be so installed and connected to



and) avoid possible confusion with circuits which do not have an elevator, nothing

in common,



(b)) it was possible to turn on the power at the load



c) movements of the lift are dependent on electrical safety devices

placed in a separate electrical safety circuit, and



(d)) a fault in the electrical installation does not cause a dangerous situation.



2. Risks to persons outside the cage



2.1. The lift must be designed and constructed so that the space in which the

cage moves, has been inaccessible except for maintenance and in emergencies.

Than the beneficiary enters into this space, it must exclude the common

the use of the elevator.



2.2. The lift must be designed and constructed so as to prevent the risk of crushing

people, if the car is in one of its extreme positions.



This requirement is satisfied by free space or escape in the

the area of the end positions.



Whereas, in special cases, in particular in the existing

buildings is not possible, this solution can be used, after the previous

the consent of the Member States of the European Union, other appropriate measures to

to prevent this risk.



2.3 Place of entry and exit of the car must be equipped with landing

doors of adequate mechanical resistance for the expected conditions

operation.



Locking device must prevent during normal operation



and starting the car, whether) the intended or unintended, as long as they are not

all landing doors are shut and locked, and



(b)) the opening of a landing door when the car is still moving and outside a

the designated landing zone.



However, commuting with the door open in a specific range for the

condition that the levelling speed is checked.



3. Risks to persons in the car



3.1 lift cars must be completely enclosed by full-length walls, full height

floors and ceilings included, with the exception of ventilation apertures, and with full-length

the door. These doors must be so designed and installed so that the

Cage cannot move unless the doors are closed, with the exception of

commuting referred to in point 2.3, and stopped, when the door is

the open.



A door shall be kept closed and secured, if the stop

between the two levels where there is risk of falling between the cage and the shaft or

If the lift is no shaft.



3.2 in the event of a power failure or failure of components must be

elevator equipped with devices to prevent free falling or

the uncontrolled movement of the cage.



The device to prevent free falling of the cage must not be dependent on hinge

the cage.



This device must be able to stop the cage at the load corresponding to the

load and at the maximum speed anticipated by the supplier. When

any load should not stop this equipment cause harmful

the slowdown for the passengers.



3.3 between the bottom of the shaft and the floor of the lift must be placed bumpers.



In this case, the free space referred to in 2.2 must be measured with a completely

compressed buffers.



This requirement does not apply to lifts in which the car due to the

the construction of the propulsion system can not get to the free space referred to in

point 2.2.



3.4. Lifts must be so designed and constructed as to make it possible to give

in motion if the device provided for in section 3.2 is not in operation.



4. Other risks



4.1 the landing doors and car doors or the two doors together, where they

motorized, must have a device against the grip of the moving door.



4.2 If the shaft door, including those with glass parts, to serve

to protect the building against fire must have adequate fire

resistance in terms of maintaining the integrity and insulation

(resistance to the effects of fire) and radiation (heat flow density in the

of fire).



4.3. Counterweights must be installed so that the

avoid any risk of colliding with or falling on the cage.



4.4. Lifts must be equipped with means enabling extrication and

the evacuation of people trapped in a cage.



4.5. The car must be fitted with two-way means of communication

allowing permanent contact with a rescue service.




4.6. Lifts must be so designed and constructed so that they can complete movements in

If the temperature in the lift machine exceeding the maximum

set by the supplier, but refuse new commands.



4.7. The car must be designed and manufactured in such a way that it is for

ensure sufficient ventilation for passengers, even in case of a longer

interruption of the operation.



4.8. The car should be adequately lit whenever in

use or a door is opened; the cage must also have emergency

lighting.



4.9. the communication referred to in section 4.5 and the emergency lighting referred to in point

4.8 must be designed and constructed so as to function even without the normal

power supply. Their function must be long enough to

allow standard rescue procedure.



4.10 control circuits of lifts which may be used in case of fire,

must be so designed and constructed as to make it possible to prevent stop

the elevator at certain levels and to allow for priority control of elevator

by rescue teams.



5. Marking



5.1 in addition to the minimum particulars required for any machine

in accordance with point 1.7.3 of annex 1 to the regulation of the Government No. 176/2008 Coll. must be

each cage is equipped with an easily visible plate clearly showing the rated

load in kilograms and the maximum number of passengers which may

be carried.



5.2 If the lift is designed to allow people trapped in the

the car to escape without outside help, the relevant instructions must be

located in a clear and visible in the car.



6. instructions



6.1 safety components for lifts specified in annex No. 3 to this

Regulation must be accompanied by instructions to the following activities could be

are carried out effectively and without danger



and Assembly)



b) connection,



c) adjustment and



(d)).



6.2 each lift must be equipped with a manual (section 29, paragraph 1 (b), (h))

of the Act). Manual contains at least the following documents:



and tutorial) drawings and diagrams necessary for normal use and

relating to maintenance, inspection, repair, periodic checks and

the rescue operations referred to in section 4.4, and



(b)) a logbook in which repairs are recorded, or regular

checks.



Č. 2



A. CONTENT OF THE EU DECLARATION OF CONFORMITY FOR SAFETY COMPONENTS FOR LIFTS



EU Declaration of conformity for safety components for lifts must

include the following information:



and business/company name) and address of the manufacturer,



(b)) or business name/style and address of the authorised representative,



c) description safety components for lifts, identification of type or series and

serial number (if any); If it is necessary to identify the

safety components for lifts, can include an image,



d) safety features safety components for lifts, if not

obvious from the description,



e) year safety components for lifts,



(f)) all the provisions under which the conformity of the safety components was

for lifts is assessed,



g) a statement that the safety component for lifts is in compliance with

all of the relevant Community harmonisation legislation of the European Union,



h) a reference to the harmonised standards, if they have been applied,



I) if was made EU type-examination of safety components

for lifts in accordance with part A of annex 4 to this Regulation: the name,

address and identification number of the notified body, that this EU

type-examination performed, and a reference to the EU type-examination certificate

This is issued by a notified body,



(j)) if it was in accordance with Annex 9 to this regulation, a procedure is executed

the assessment of conformity to type with random checking, as regards

safety components for lifts: the name, address and identification

the number of the notified body which has performed the conformity-assessment procedure,



k) if it has approved the quality system used by the manufacturer in accordance with the

conformity assessment procedure according to annex No 6 or 7 to this Regulation:

the name, address and identification number of the notified body

This quality system approved.



l) name and function of the persons empowered to sign the Declaration on behalf of the manufacturer

or his authorised representative,



m) place and date of the signing and



n) signature.



B. CONTENT OF THE EU DECLARATION OF CONFORMITY FOR LIFTS



EU Declaration of conformity for lifts must be drafted in the same language

as the instructions referred to in section 6.2 of annex 1 to this regulation and shall

include the following information



and business/company name) and address of the manufacturer,



(b)) or business name/style and address of the authorised representative,



(c) a description of the lift, the designation) type or series, serial number and the address where

the lift is installed,



(d) the installation of the lift, year)



(e)) all the provisions under which the conformity of the lift was assessed,



f) Declaration that the elevator is in conformity with the relevant Community harmonisation

the legislation of the European Union,



g) a reference to the harmonised standards, if they have been applied,



h) if the EU type-examination was made of the lift in accordance with part B of the

of annex 4 to this Regulation: the name, address and identification

the number of the notified body, that the EU type-examination of a lift

carried out, and a reference to the EU type-examination certificate, the notified

the body issued,



even if it was in accordance with annex) # 8 this regulation carried out the procedure

conformity assessment unit verification as to the

Elevators: the name, address and identification number of the notified body,

that made this the conformity assessment procedure,



j) If, pursuant to annex 5 to this regulation made

final inspection of the lift: the name, address and identification number of the

the notified body which carried out the final inspection of the lift,



to) if it was approved quality assurance system used by

the supplier in accordance with the conformity assessment procedure according to annex No 10,

11 or 12 of this Regulation: the name, address and identification number of the

the notified body which has approved the quality assurance system.



l) name and function of the persons empowered to sign the Declaration on behalf of the vendor

or his authorised representative,



m) place and date of the signing and



n) signature.



Č. 3



THE LIST OF SAFETY COMPONENTS FOR LIFTS



1. Devices for locking landing doors.



2. the Device referred to in point 3.2 of annex 1 to this regulation, which

to prevent falling or uncontrolled movements.



3. overspeed limitation Devices.



4.



and Bumpers: akumulující energy)



I) nonlinear, or



II) with damping of the return movement;



(b)) energy absorbing Bumpers.



5. Safety devices fitted to jacks of hydraulic power

the circuit used as devices to prevent falls.



6. Electric safety devices the safety represented by the

circuits with electronic components.



Č. 4



THE EU TYPE-EXAMINATION OF LIFTS AND SAFETY COMPONENTS FOR LIFTS



(module B)



The EU type-examination and safety components for lifts



1. the EU type-examination is the part of a conformity assessment procedure in which

the notified body examines the technical design of the safety component for

lifts and verifies and attests that the technical design of the safety component

for lifts complies with the relevant basic technical requirements and allow the

to satisfy those requirements the lift in which the safety component

properly built.



2. the manufacturer or his authorised representative shall submit with a single notified

body of his choice, the request of the EU type-examination.



The application must include



and the name and address of the manufacturer), and if the application is lodged by the authorised representative,

his name and address and the place of manufacture of the safety components for

elevators,



(b)) a written declaration that the same application has not been lodged with any other

a notified body,



(c)) the technical documentation,



d) representative specimen of the safety components for lifts or data

a place where it can be checked, and the notified body may

request further specimens if needed for the implementation of the programme

tests, and



(e) supporting evidence for the adequacy of) the solution adopted in the technical proposal.

This supporting evidence shall mention any relevant documents,

that have been used, including other relevant technical specifications,

in particular where the relevant harmonised standards have not been applied in full

the range. Supporting evidence, if necessary, include the results of tests,

carried out in accordance with other relevant technical specifications

Laboratory of the manufacturer, or by another testing laboratory on his behalf and under his

liability.



3. the technical documentation must enable an assessment of whether the security

component for lifts meets the conditions referred to in paragraph 1, and include the

adequate analysis and risk assessment. The technical documentation must

specify the applicable requirements and to the extent necessary for the assessment,

cover the design, manufacture and operation of the safety component for

elevators.



The technical documentation shall contain, where relevant, the

requirements:



and) description safety components for lifts, including the area of use

(in particular possible limits on speed, load and power) and conditions

(in particular explosive environments and exposure to the elements),



b) design and manufacturing drawings and diagrams,




c) explanations necessary for the understanding of said drawings and schemes and the

the functioning of safety components for lifts,



(d)) the list of harmonized standards, references to which have been published in the

The official journal of the European Union and which have been applied in full

or in part, and descriptions of the solutions adopted to security

component for lifts to meet one or both of the conditions referred to in

point 1, where those harmonised standards have not been applied, and a list of other

the relevant technical specifications which were used. In the case of

partially applied harmonised standards, the technical documentation

shall specify the parts which have been applied,



e) results of design calculations carried out by the manufacturer or

the manufacturer,



f) test reports,



(g) a copy of the instruction manual) safety components for lifts and



h) measures carried out at the production stage to ensure that series-

the manufactured safety components for lifts were identical with controlled

safety component for the elevators.



4. the notified body



a) examine the technical documentation and supporting evidence to assess the

the adequacy of the technical design of the safety components for lifts,



b) agree with the applicant, at which point the examinations and tests

carried out,



c) verifies that he was a representative sample (s) (s) (s) made in the

conformity with the technical documentation and identify the elements which have been designed in

accordance with the applicable provisions of the relevant harmonised standards, the

and elements which have been designed in accordance with other relevant technical

specifications,



(d)) carries out or causes perform appropriate examinations and tests in order to check

whether, where the manufacturer has chosen to apply the relevant specifications

harmonised standards, these have been applied correctly, the



e) carries out or causes perform appropriate examinations and tests in order to check

whether, where the appropriate specifications have not been applied

harmonised standards, allow you to other relevant

the technical specifications used by the manufacturer to the safety

component for lifts to meet the conditions referred to in paragraph 1.



The notified body shall draw up an evaluation report that records the

examinations, checks and tests and their results. Without prejudice to the

without prejudice to the obligations of the notified body to the authority for technical

Standardization, metrology and testing (hereinafter referred to as "the authority"),

the notified body shall release the content of this report, in full or in

in part, only with the consent of the manufacturer.



5. If the type of safety components for lifts meets the conditions

referred to in point 1, the notified body shall issue a certificate to the manufacturer of the EU

type-examination. This certificate must contain the name and address of the

the manufacturer, the conclusions of the EU type-examination, conditions for its validity and the

the necessary data for identification of the approved type.



The EU type-examination certificate may be accompanied by 1 or more

attachments.



The EU type-examination certificate and its annexes shall contain all

appropriate information to allow evaluation of whether they are produced

safety components for lifts in accordance with the examined type and

perform a check in operation.



If the type of safety components for lifts does not meet the conditions referred to

in point 1, the notified body shall refuse to issue a certificate of EU type examination

and shall inform the applicant accordingly, giving detailed reasons for such denial denial.



The notified body shall keep a copy of the EU type-examination certificate, its

annexes and additions, as well as technical documentation and evaluation report after

period of 15 years from the date of issue of this certificate.



6. the notified body shall ensure that it is kept informed of any changes

the generally acknowledged State of the art which indicate that the approved

type may no longer comply with the conditions laid down in paragraph 1, and

shall determine whether such changes require further investigation. If the investigation

require, the notified body shall inform the manufacturer.



7. The manufacturer shall inform the notified body that holds the technical

the documentation concerning the EU type-examination certificate of all

modifications to the approved type that may affect the conformity of the safety

components for lifts with the conditions referred to in point 1 or conditions

the EU type-examination certificate validity.



The notified body shall examine the modifications and inform the applicant whether

the EU type-examination certificate remains valid, or whether they are

need for additional review, verification or examination. The notified body

may be issued by the appendix to the original EU type-examination certificate; in

other cases, the manufacturer or his authorised representative shall proceed

According to section 2 of this part of the annex.



8. each notified body shall inform the authority of the EU type-examination certificates

type and any additions thereto which it has issued or withdrawn, and shall, periodically or on

request, make available to the authority the list of certificates and/or additions thereto which it

refused, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

the EU type-examination certificates and/or any additions thereto which it has refused,

withdrawn, suspended or otherwise restricted, and, upon request, about the certificates and

additions thereto which it has issued.



9. the European Commission, European Union Member States and the other notified

bodies may request a copy of the certificate, the notified body for the EU

type-examination or additions to them. The European Commission and the Member States

The European Union may apply to the notified body for a copy of the technical

documentation and reports on the examinations and tests carried out by him, the verifications

carried out.



10. The manufacturer must keep with the technical documentation a copy of certificates

The EU type-examination certificate, its annexes and additions at the disposal of the supervisory authority

After a period of 10 years after the safety components for lifts on the market.



11. The authorized representative



Manufacturer's authorised representative may lodge the application referred to in point 2 and

carry out the activities provided for in paragraphs 7 and 10, if in a manufacturer's credentials

authorised representative established.



(B) the EU type-examination of lifts.



1. the EU type-examination is the part of a conformity assessment procedure in

that a notified body examines the technical design of the model lift or

the elevator, for which no action has been made for the extension of, or

replacement, and verifies and attests that the technical design of the model lift or

the lift complies with the relevant basic technical requirements.



Part of the EU type-examination of a lift is the examination of a representative

a sample of the complete lift.



2. the contractor or his authorised representative shall submit with a single notified

the body which chose the notified body, which chose,

the EU type-examination request.



The application must include



and) the name and address of the supplier 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 any other

a notified body,



(c)) the technical documentation,



d) details of the place where the sample may be tested, with a sample of the lift

the elevator ready for examination must be in the final and

be able to use at least 3 stations (upper, middle and lower), and



(e) supporting evidence for the adequacy of) the solution adopted in the technical proposal.

This supporting evidence shall mention any relevant documents,

that have been used, including other relevant technical specifications,

in particular where the relevant harmonised standards have not been applied in full

the range. Supporting evidence, if necessary, include the results of tests,

carried out in accordance with other relevant technical specifications

laboratory supplier or by another testing laboratory on his behalf and under his

liability.



3. the technical documentation must enable the conformity of the lift with the

the relevant essential requirements.



The technical documentation shall contain, where relevant, the

requirements:



and a description of the model lift) with a clear indication of all permitted modifications

the model lift,



b) design and manufacturing drawings and diagrams,



c) explanations necessary for the understanding of said drawings and schemes and the

operation of the lift,



(d) consideration of the basic list) of the technical requirements,



(e)) the list of harmonized standards, references to which have been published in the

The official journal of the European Union and which have been applied in full

or in part, and descriptions of the solutions adopted to meet the essential technical

the requirements laid down in this regulation, where those harmonised standards

have not been applied, and a list of other relevant technical specifications,

that were used. In the event of partly applied harmonised standards

the technical documentation shall specify the parts which have been applied,



f) copy of the EU Declaration of conformity safety components for lifts

in the elevator,



g) results of design calculations carried out by or for the

the vendor,



h) test reports,



(I) a copy of the instructions) according to section 6.2 of annex 1 to this regulation and



j) measures carried out in the installation stage to ensure that series-

produced by elevators meet the essential technical requirements.



4. the notified body



a) examine the technical documentation and supporting evidence to assess the

the adequacy of the technical design of the model lift or elevator, which


There is no provision for an extension or renewal,



b) agree with the supplier, at which point they will review and

tests carried out,



(c) examine the sample lift with) in order to verify that it has been manufactured in accordance with

the technical documentation and identify the elements which have been designed in accordance with the

the applicable provisions of the relevant harmonised standards and elements

which have been designed in accordance with other relevant technical

specifications,



(d)) carries out or causes perform appropriate examinations and tests in order to check

whether in the case where a supplier has chosen to apply the relevant specifications

harmonised standards, these have been applied correctly, the



e) carries out or causes perform appropriate examinations and tests in order to check

whether, where the appropriate specifications have not been applied

harmonised standards, supplier of solutions applied under other

relevant technical specifications meet the relevant basic

technical requirements.



5. the notified body shall draw up an evaluation report that records the

examinations, checks and tests and their results. Without prejudice to the

without prejudice to the obligations of the notified body to the authority, the notified body

contents of this report shall be published, in full or in part, only with the

the agreement of the supplier.



6. Where the type meets the basic technical requirements that apply to

the elevator, the notified body shall issue a certificate to the supplier of the EU

type-examination. This certificate must contain the name and address of the

the vendor, the conclusions of the EU type-examination, conditions for its validity

and the necessary data for identification of the approved type.



The EU type-examination certificate may be accompanied by 1 or more

attachments.



The EU type-examination certificate and its annexes shall contain all

information necessary to enable it to be at the final inspection

conformity of the lifts with the approved type.



If the type does not satisfy the basic technical requirements, the notified body

refuses to issue EU type-examination certificate and shall inform the

the vendor, with the refusal of the refusal.



The notified body shall keep a copy of the EU type-examination certificate, its

annexes and additions, as well as technical documentation and evaluation report after

period of 15 years from the date of issue of this certificate.



7. the notified body shall ensure that it is kept informed of any changes

the generally acknowledged State of the art which indicate that the approved

type may no longer comply with the basic technical requirements, and

shall determine whether such changes require further investigation. If the investigation

require, the notified body shall inform the supplier.



8. the supplier shall inform the notified body of any modifications to the approved type,

including adjustments not listed in the original technical dossier, which may

affect the conformity of the lift with the essential technical requirements or conditions

the EU type-examination certificate validity.



The notified body shall examine the change and shall inform the supplier about whether

the EU type-examination certificate remains valid, or whether they are

need for additional review, verification or examination. The notified body

may be issued by the appendix to the original EU type-examination certificate; in

other cases, the manufacturer or his authorised representative shall proceed

referred to in point 2. This part of the annex.



9. each notified body shall inform the authority of the EU type-examination certificates

type and any additions thereto which it has issued or withdrawn, and shall, periodically or on

request, make available to the authority the list of certificates and/or additions thereto which it

refused, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

the EU type-examination certificates and/or any additions thereto which it has refused,

withdrawn, suspended or otherwise restricted, and, upon request, about the certificates and

additions thereto which it has issued.



10. the European Commission, European Union Member States and the other notified

bodies may request a copy of the certificate, the notified body for the EU

type-examination or additions to them. The European Commission and the Member States

The European Union may apply to the notified body for a copy of the technical

documentation and reports on the examinations and tests carried out by him, the verifications

carried out.



11. the supplier shall keep with the technical documentation a copy of certificates

The EU type-examination certificate, its annexes and additions, including the disposal of the body

supervision for a period of 10 years after the lift on the market.



12. Authorized Representative



The authorized representative of the vendor may lodge the application referred to in point 2 and

carry out the activities provided for in paragraphs 8 and 11, if that producer in credentials

authorised representative established.



Č. 5



FINAL INSPECTION OF THE LIFTS



1. final inspection is the part of a conformity assessment procedure, which

a notified body ascertains and certifies that a lift which is the subject of

the EU type-examination certificate, or which is designed and manufactured according to the

the approved quality system, meets the basic technical requirements.



2. the activities of the SUPPLIER



The contractor shall take all necessary measures to ensure that the lift which is

installed to satisfy the relevant basic technical requirements and one of the

the following requirements:



a) is in accordance with the approved type described in the certificate of the EU

type-examination certificate, or



(b)) is designed and manufactured in accordance with a quality system in accordance with Annex No.

11 to this regulation and the EU design examination certificate, if

is not wholly in accordance with the harmonized standards.



3. final inspection



A notified body chosen by the supplier will carry out the final inspection

the lift about to be placed on the market in order to verify the conformity of the lift with the

the relevant essential requirements.



3.1 the supplier shall submit a request for final inspection with a single notified

body of his choice, and the notified body shall provide the

documents:



and the drawing of the complete lift sestavný),



(b)) the drawings and diagrams necessary for final inspection, in particular schemes

control circuit,



c) instructions referred to in point 6.2 of annex 1 to this regulation and



(d)) a written declaration that the same application has not been lodged with any other

of the notified body.



The notified body may not require detailed plans or precise

information that is not necessary for verifying the conformity of the lift.



Must be performed the appropriate examinations and tests as set out in the

the relevant harmonised standard (s) or equivalent tests, in order to

ensure to check the conformity of the lift with the relevant essential

technical requirements.



3.2 the review must include at least 1 of the following:



and review of documents) referred to in point 3.1 in order to verify whether the

the lift conforms with the approved type as described in the EU type-examination certificate

referred to in part B of annex 4 to this regulation,



(b)) review of documents referred to in point 3.1 in order to verify whether the

the lift conforms with the lift, designed and manufactured in accordance with the approved

quality system in accordance with Annex 11 of this regulation and with the certificate

The EU review of the design, if the design is not entirely in accordance with the

the harmonized standards.



3.3. The test must include at least the following steps:



and operation of the lift both empty and at maximum) of a loaded lift in order to verify

correct installation and operation of the safety devices (for example, end

switches, locking devices),



(b) the operation of the elevator) at maximum load and no load to verify the

the correct operation of the safety devices in the event of a power failure,



(c) static load test) equal to 25 times the nominal

load.



Rated load conforms to section 5 of annex 1 to this regulation.



After these tests, the notified body shall check that there is no

deformation or damage that could impair the use of the lift.



4. If the lift satisfies the basic technical requirements, the notified

body shall affix, or cause to be positioned next to the CE marking of your identification

number in accordance with § 14 and shall draw up a final inspection certificate, in

the examinations and tests shall be carried out.



The notified body shall fill in the corresponding pages of the logbook referred to in section 6.2.

Annex 1 to this regulation.



If the notified body refuses to issue the final inspection certificate, this

detailed reasons for refusal, indicating the necessary corrective measures, which

to be taken. If the supplier again applies for final inspection,

must apply to the same notified body.



5. the CE marking and EU Declaration of conformity



5.1 Contractor placed in a cage of each lift, which meets the basic

the technical requirements of the CE marking, and placed next to the CE marking in the cage

each lift the identification number of the notified body referred to in point

3.1.



5.2 the supplier shall draw up a written EU Declaration of conformity for each elevator and

a copy of the EU Declaration of conformity and the final inspection certificate stores

the disposal of the supervisory authorities for 10 years after the lift on the market.

A copy of the EU Declaration of conformity on request provide the supervisory authority.



6. the European Commission and the Member States of the European Union may apply to the notified

the body of the copy of the certificate of final inspection.



7. Authorized Representative



Supplier's activities set out in points 3.1 and 5 may be on his behalf and

under his responsibility fulfilled by his authorised representative, if


the manufacturer's authorised representative established in the mandate.



Č. 6



CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTS IN TERMS OF

SAFETY COMPONENTS FOR LIFTS



(module E)



1. conformity to type based on quality assurance of the products in terms of

safety components for lifts, is the part of a conformity assessment procedure

the notified body assesses the quality system of the manufacturer in order to

to ensure that safety components for lifts are manufactured and

monitored so that they are in conformity with the type as described in the certificate of the EU

type-examination, comply with the relevant requirements of annex 1 to this

Regulation and, in order to satisfy those requirements lift to which they are

properly built.



2. the activities of the manufacturer



The manufacturer must operate an approved quality system for final inspection and

the examination of safety components for lifts specified in point 3 and shall be subject to

surveillance as specified in point 4.



3. quality system



3.1. the manufacturer lodges an application for the safety components for lifts with a single

notified body of his choice, the request for an assessment of your system

the quality.



The application must include



and) 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 any other

a notified body,



c) address space, where he performs final inspection and tests

safety components for lifts



d) all relevant information on safety components for

elevators, which are to be manufactured,



(e)) the documentation concerning the quality system, and



f) technical documentation for the approved safety components

lifts and a copy of the EU type-examination certificate.



3.2. Under the quality system, each safety component must be for

lifts must be examined and appropriate tests as set out in made

relevant harmonised standards, or equivalent tests, to

ensure to comply with the conditions referred to in paragraph 1. All the elements,

requirements and provisions adopted by the manufacturer must be systematically and

orderly manner in the form of written measures, procedures and instructions.

This quality system documentation must permit a consistent interpretation

programmes, plans, manuals and records relating to quality.



This quality system documentation shall contain in particular an adequate description of the



and) the objectives in terms of quality,



(b)) the organizational structure, responsibilities and powers of the management with regard to

the quality of products,



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



(d)) the means of monitoring the efficient operation of the system

the quality and



(e)) the quality records, such as inspection reports and records of the

tests carried out, records of calibration reports

the qualifications of the personnel concerned, etc.



3.3 the notified body shall assess the quality system to determine whether it satisfies

the requirements referred to in 3.2. The elements of the quality system that conform to the

the relevant specifications of the relevant harmonised standards, compliance with these

the requirements of the standard.



Persons who, on behalf of the notified body shall carry out an assessment of the system

quality, (hereinafter referred to as "audit team") must have experience with systems

quality control and at least one Member must have experience with

assessment of the technology of lifts and knowledge of basic technical

requirements.



The audit includes an assessment visit to the manufacturer's premises.



Auditing team shall review the technical documentation referred to in point 3.1.

(a). (f)), to verify the manufacturer's ability to identify the relevant requirements of

laid down in this regulation and to carry out the necessary examinations in order to ensure

the compliance of the safety components for lifts with these requirements.



The conclusions of the audit, including the reasons therefor shall be notified to the manufacturer.



3.4. the manufacturer must undertake to fulfil the obligations arising from the

the quality system as approved and to maintain it so that it

remains adequate and efficient.



3.5. The manufacturer or his authorised representative shall keep the notified body,

that has approved the quality system informed of any intended change of the quality system.



The notified body must assess the changes proposed and decide whether the modified

the quality system will still satisfy the requirements referred to in point 3.2,

or whether a re-assessment is required.



The notified body shall notify the manufacturer, the conclusions of his review, including their

justification.



4. supervision of the notified body



4.1. The purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations

arising out of the approved quality system.



4.2. the manufacturer must allow the notified body in order to assess access to

the space where the final inspection is carried out, testing and storage, and

provide it with all necessary information, in particular



and quality system documentation)



(b)) the technical documentation, and



(c)) the quality records, such as inspection reports and records from the

tests carried out, records of the performed calibration,

the qualifications of the staff concerned.



4.3. the notified body must periodically carry out audits to make sure that

manufacturer maintains and applies the quality system and shall provide the manufacturer detail about

audit.



4.4. Additionally, the notified body may make unannounced inspection

visits at the premises of the manufacturer, where he performs a final inspection and

the examination of safety components for lifts.



During such visits the notified body may, if necessary,

or have carried out tests to verify that the quality system is functioning correctly.

The notified body must provide the manufacturer with a visit report and the Protocol on

the tests have been carried out.



5. the CE marking and EU Declaration of conformity



5.1 the manufacturer shall affix the CE marking and the identification number of the notified

body referred to in point 3.1, on each individual safety component

for lifts, which satisfies the conditions referred to in point 1.



5.2. the manufacturer shall draw up for each safety component for lifts

EU Declaration of conformity in writing and a copy of it must, for organ

supervision for a period of 10 years after the safety components for lifts on

the market. The EU Declaration of conformity shall identify the safety component

for lifts, for which it has been drawn up.



6. The manufacturer shall keep at the disposal of the supervisory authority for a period of 10 years after the

safety components for lifts on the market



and) the technical documentation referred to in point 3.1 (b). (f)),



(b)) the documentation referred to in point 3.1 (b). (e)),



c) information about the change referred to in point 3.5 and the



(d)) the conclusions and reports of the notified body which are referred to in

points 3.5, 4.3 and 4.4.



7. each notified body shall inform the authority about the certifications of the approval

quality system issued or withdrawn, and shall, periodically or upon request,

the Office shall make available a list of the approval certificate, which it has refused

, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

certificates of quality system approvals which it has refused

suspended or withdrawn, and, on request, about certificates of approval

It has issued.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of quality system approval

It has issued.



8. Authorized Representative



The manufacturer's activities set out in points 3.1, 3.5, 5 and 6 may be

behalf and under his responsibility fulfilled by his authorised representative,

If the manufacturer's authorised representative established in the mandate.



Č. 7



CONFORMITY BASED ON FULL QUALITY ASSURANCE, AS REGARDS THE

SAFETY COMPONENTS FOR LIFTS



(module H)



1. conformity based on full quality assurance, as regards the

safety components for lifts is the conformity assessment procedure

which the notified body assesses the quality system of the manufacturer in order to

to ensure that safety components for lifts were designed,

manufactured, inspected and tested to comply with the relevant

the requirements of annex 1 to this regulation and to ensure that these

meet the requirements of lift to which they are correctly fitted.



2. the activities of the manufacturer



The manufacturer must operate an approved quality system for design, manufacture,

final inspection and testing of safety components for lifts by

point 3 and shall be subject to surveillance as specified in point 4.



3. quality system



3.1. The manufacturer lodges an a single notified body of his choice,

application for assessment of his quality system. The application must include



and the name and address of the manufacturer), and if the application is lodged by the authorised representative,

his name and address,



(b)) address space, where there are safety components for lifts

designed, manufactured, inspected and tested,



(c)) all relevant information on safety components for

elevators, which are to be manufactured,



(d) the technical documentation described in section), and point 3 of annex 4 to this

Regulation for one model of each category of safety components for

elevators, which is to be produced,



(e) quality and system documentation)



(f)) a written declaration that the same application has not been lodged with any other

of the notified body.



3.2. the quality system shall ensure compliance of the safety components

for lifts with the conditions referred to in point 1. All the elements, requirements

and provisions adopted by the manufacturer must be systematic and orderly

documented in the form of written measures, procedures and instructions. This


the quality system documentation must permit a consistent interpretation of the programs,

plans, manuals and records relating to the quality.



Production quality assurance system documentation must include in particular the

an adequate description



and) the objectives in terms of quality and the organisational structure, responsibilities and

powers of the management with regard to design and product quality,



(b)) the technical design specifications, including standards, that will be used, and

in the case that the relevant harmonised standards shall not be used or

not apply in full, the means, including other relevant

technical specifications, that will be used to ensure

compliance with the conditions referred to in paragraph 1,



c) inspection and design verification techniques, processes and systematic

the activities that will be used when designing the safety components for

elevators,



(d)) of the respective techniques, processes and systematic actions that are

used in the manufacture, control and quality assurance,



(e)) of the examination and tests that will be carried out before, during

and after manufacture, the frequency with which,



(f)) the quality records, such as inspection reports and records of the

tests carried out, records of calibration reports

the qualifications of the personnel concerned, and



g) the means of monitoring the achievement of the required quality

the design and the product and the efficient operation of the quality system.



3.3 the notified body shall assess the quality system to determine whether it satisfies

the requirements referred to in 3.2. The elements of the quality system that conform to the

the relevant specifications of the relevant harmonised standards, compliance with these

the requirements of the standard.



The auditing team must have experience in quality management systems and at least

one Member must have experience of assessments of the technology concerned

lift the techniques and knowledge of the basic technical requirements. Audit

shall include an assessment visit to the manufacturer's premises.



Auditing team shall review the technical documentation referred to in point 3.1.

(a). (d)), to verify the manufacturer's ability to identify the relevant essential

technical requirements and carry out the necessary review to ensure

the compliance of the safety components for lifts with these requirements.



The notified body shall inform the manufacturer or his authorised representative

the conclusions of the audit, including the reasons therefor.



3.4. the manufacturer must undertake to fulfil the obligations arising from the

the quality system as approved and to maintain it so that it

remains adequate and efficient.



3.5. The manufacturer shall inform the notified body that has approved the quality system,

of any intended change of the quality system.



The notified body must assess the changes proposed and decide whether the modified

the quality system will still satisfy the requirements referred to in point 3.2,

or whether a re-assessment is necessary.



The notified body shall notify the manufacturer, the conclusions of its assessment, including their

justification.



4. supervision of the notified body



4.1. The purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations

arising out of the approved quality system.



4.2. the manufacturer must allow the notified body in order to assess access to

the places of design, manufacture, inspection and testing, and

storage and must provide it with all necessary information, in particular



and quality system documentation)



(b)) the quality records provided for in part of the quality system relating to

the design, such as results of analyses, calculations, tests,



(c)) the technical documentation relating to the manufactured safety

components for lifts and



(d)) the quality records provided for in the manufacturing part of the quality system,

for example, the reports of the inspections, the records of the tests carried out,

records of the performed calibration, reports on the qualifications of the relevant

workers, etc.



4.3. the notified body shall carry out periodic audits to make sure that

manufacturer maintains and applies the quality system and shall provide the manufacturer detail about

audit.



4.4 in addition, the notified body may pay the manufacturer unannounced

visits. During such visits the notified body may

If necessary, carry out or have carried out tests to verify that the

the quality system is functioning correctly. The notified body must provide the manufacturer detail

about your visit and log on the tests, if tests have been carried out.



5. the CE marking and EU Declaration of conformity



5.1 the manufacturer shall affix the CE marking and the identification number of the notified

body referred to in point 3.1, on each individual safety component

for lifts, which satisfies the conditions referred to in point 1.



5.2. the manufacturer shall draw up for each safety component for lifts

EU Declaration of conformity in writing and a copy of it must, for organ

supervision for a period of 10 years after the safety components for lifts on

the market. The EU Declaration of conformity shall identify the safety component

for lifts, for which it has been drawn up.



6. The manufacturer shall keep at the disposal of the supervisory authority for a period of 10 years after the

safety components for lifts on the market



and the documentation referred to in point), 3.1 (b). (e)),



(b)) the technical documentation referred to in point 3.1 (b). (d)),



c) information about the change referred to in point 3.5 and the



(d)) the conclusions and reports of the notified body referred to in points 3.5,

4.3 and 4.4.



7. each notified body shall inform the authority about the certifications of the approval

quality system issued or withdrawn, and shall, periodically or upon request,

the Office shall make available a list of the approval certificate, which it has refused

, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

certificates of quality system approvals which it has refused

suspended or withdrawn, and, on request, about certificates of approval

It has issued.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of quality system approval

It has issued.



The notified body shall keep a copy of the approval certificate, which it has issued,

its annexes and additions, as well as the technical documentation for a period of

15 years from the date of their issue.



8. Authorized Representative



The manufacturer's activities set out in points 3.1, 3.5, 5 and 6 may be

behalf and under his responsibility fulfilled by his authorised representative,

If the manufacturer's authorised representative established in the mandate.



Č. 8



CONFORMITY BASED ON UNIT VERIFICATION AS TO THE

LIFTS



(module G)



1. conformity based on unit verification is the procedure

conformity assessment, whereby a notified body assesses whether the lift complies with the

the basic technical requirements.



2. the activities of the supplier



2.1 the contractor shall take all necessary measures to ensure that the manufacturing process and

its monitoring ensure conformity of the lift with the relevant essential

technical requirements.



2.2 the contractor shall submit with a single notified body of his choice,

application for a unit verification.



The application must include



and the name and address of the supplier), and if the application is lodged by the authorized

Representative, his name and address,



b) details of the place where the lift is installed,



c) a written declaration that a similar application has not been lodged with any other

the notified body, and



(d) the technical documentation).



3. the technical documentation must enable the conformity of the lift with the

the relevant essential requirements.



The technical documentation shall contain at least the following information



description of the lift, and)



b) conceptual design and manufacturing drawings and schemes of components,



c) explanations necessary for the understanding of said drawings and schemes and the

operation of the lift,



(d) a list of the measured Basic) technical requirements,



(e)) the list of harmonized standards, references to which have been published in the

The official journal of the European Union and which have been applied in full

or in part, and descriptions of the solutions adopted to meet the essential technical

the requirements laid down in this regulation, where those harmonised standards

have not been applied, and a list of other relevant technical specifications,

that were used. In the event of partly applied harmonised standards

the technical documentation shall specify the parts which have been applied,



f) copy of the EU type-examination certificate of safety components for

the elevators in the elevator,



g) results of design calculations carried out by or for the

the vendor,



h) test reports and



(I) a copy of the lift instruction manual) referred to in section 6.2 of annex 1 to this regulation.



4. verification of the



A notified body chosen by the supplier to examine the technical documentation and

lift and carry out the appropriate tests as set out in the relevant harmonised

standard (s) or equivalent tests, to ensure the review

conformity of the lift with the relevant essential requirements. Tests

must include at least the tests referred to in point 3.3 of annex 5 to this

of the regulation.



If the lift meets the basic technical requirements, the notified body

shall draw up a certificate of conformity relating to the tests carried out.



The notified body shall fill in the corresponding pages of the logbook referred to in section 6.2.

Annex 1 to this regulation.



If the notified body refuses to issue a certificate of conformity, this fact

refusal, indicating the necessary corrective measures to be

taken. If the supplier once again asks for unit verification


the product shall apply to the same notified body.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of compliance.



5. the CE marking and EU Declaration of conformity



5.1 Contractor placed in a cage of each lift, which meets the basic

the technical requirements of the CE marking, and placed next to the CE marking in the cage

each lift the identification number of the notified body referred to in point 2.2.



5.2 the supplier shall draw up a written EU Declaration of conformity for each elevator and

a copy of the EU Declaration of conformity shall keep at the disposal of the supervisory authority for

10 years after the lift on the market. A copy of the EU Declaration of conformity

the request shall provide the supervisory authority.



6. the supplier shall keep the technical documentation and a copy of the certificate of conformity

the disposal of the supervisory authority for a period of 10 years from the date on which the lift is placed

on the market.



7. Authorized Representative



Supplier's activities set out in points 2.2 and 6 may be on his behalf and

under his responsibility fulfilled by his authorised representative, if

the manufacturer's authorised representative established in the mandate.



Č. 9



CONFORMITY TO TYPE WITH RANDOM CHECKING BY SELECTING AS REGARDS SAFETY

COMPONENTS FOR LIFTS



(module 2)



1. conformity to type with random Checking by selecting the part of the assessment process

the conformity of the notified body carries out checks on safety

components for lifts in order to ensure that they are in conformity with the approved

type as described in the EU type-examination certificate, comply with the relevant

the requirements of annex 1 to this regulation and to ensure that these

meet the requirements of lift to which they are correctly fitted.



2. production



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

monitoring ensure that the manufactured safety components for lifts

meet the conditions laid down in paragraph 1.



3. the manufacturer lodges an application with a single notified body of his choice, the request

about the random control.



The application must include



and the name and address of the manufacturer), and if the application is lodged by the authorised representative,

his name and address,



(b)) a written declaration that the same application has not been lodged with any other

a notified body,



(c)) all relevant information on the manufactured safety components

for elevators and



d) information about the premises where the sample may be removed for safety

components for lifts.



4. the notified body shall carry out or have carried out checks on safety

components for lifts at random intervals. The notified body

Removes the on the spot an adequate sample of the finished safety

components for lifts, which must be examined and subjected to

appropriate tests set out in the relevant harmonised standards

or equivalent tests laid down in other relevant technical

specifications in order to verify whether the security component for lifts

satisfies the conditions laid down in paragraph 1. In the event that one or more of the

under the safety components for lifts is not in conformity,

the notified body shall take appropriate measures.



Aspects that should be taken into account when checking security

components for lifts, will be fixed by common agreement of all

notified bodies dealing with this procedure, taking in the

account of the basic parameters of safety components for lifts.



The notified body shall issue a certificate of conformity with the type having regard to carried out

examinations and tests.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of compliance type.



5. the CE marking and EU Declaration of conformity



5.1 the manufacturer shall affix the CE marking and the identification number of the notified

body referred to in point 3 to each individual safety component for

elevators, which satisfies the conditions referred to in point 1.



5.2. the manufacturer shall draw up for each safety component for lifts

EU Declaration of conformity in writing and a copy of it must, for organ

supervision for a period of 10 years after the safety components for lifts on

the market. The EU Declaration of conformity is given a safety component for

lifts, for which it has been drawn up.



6. Authorized Representative



The activities of the manufacturer can be on his behalf and under his responsibility fulfilled

his authorised representative, if this manufacturer in the mandate

authorised representative established. The authorized representative may not fulfil the

the activities of the manufacturer referred to in point 2.



Č. 10



CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTS IN TERMS OF

LIFTS



(module E)



1. conformity to type based on quality assurance of the products is part of the

conformity assessment procedure whereby a notified body assesses the system

the quality of the vendor's product in order to ensure that the lifts were in line

with the approved type as described in the EU type-examination certificate, or

an elevator designed and made in the context of a complete system of quality

approved in accordance with Annex 11 to this regulation and comply with the

the basic technical requirements.



2. the activities of the supplier



The supplier shall operate an approved quality system for final inspection and

testing of lifts according to point 3 and shall be subject to surveillance as specified in point 4.



3. quality system



3.1 the supplier shall submit with a single notified body of his choice,

application for assessment of his quality system for the lifts.



The application must include



and the name and address of the supplier), and if the application is lodged by the authorized

Representative, his name and address,



(b)) all relevant information on the lifts, which are to be

installed,



(c) quality system documentation)



(d)) the technical documentation of lifts which are to be installed, and



e) a written declaration that the same application has not been lodged with any other

of the notified body.



3.2. Under the quality system, each lift must be examined and must

be made to the appropriate tests as set out in the relevant harmonised

standards, or equivalent tests, to ensure its conformity with the

the relevant essential requirements.



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

a systematic and orderly manner in the form of written policies,

procedures and instructions. This quality system documentation must permit a

uniform interpretation programmes, plans, manuals and records relating to the

the quality.



This quality system documentation shall contain in particular an adequate description of the



and) the objectives in terms of quality,



(b)) the organizational structure, responsibilities and powers of the management with regard to

the quality of products,



(c)) the examination and tests that will be carried out before placing on the market,

at least including the tests referred to in point 3.3 of annex 5 to this

Regulation,



(d)) the means of monitoring the efficient operation of the system

the quality and



(e)) the quality records, such as inspection reports and records of the

tests carried out, records of calibration reports

the qualifications of the staff concerned.



3.3 the notified body shall assess the quality system to determine whether it satisfies

the requirements referred to in 3.2. The elements of the quality system that conform to the

the relevant specifications of the relevant harmonised standards, compliance with these

the requirements of the standard.



In the auditing team must have at least one member with experience of

the elevator technology assessment techniques and knowledge of the basic

technical requirements. The audit includes an assessment visit to the premises of the

the premises of the supplier and on the place of installation of the lift.



The conclusions of the audit, including the reasons therefor shall be notified to the supplier.



3.4 the supplier shall undertake to fulfil the obligations arising from the

the quality system as approved and to maintain it so that it

remains adequate and efficient.



3.4.1. The contractor shall inform the notified body that has approved the system

the quality of any intended change to the system.



3.4.2. The notified body must assess the changes proposed and decide whether the modified

the quality system will still satisfy the requirements referred to in point 3.2,

or whether a re-assessment is necessary.



The notified body shall notify the supplier of the conclusions of its review, including

their justification.



The notified body shall affix, or cause to be positioned next to the CE marking of your

identification number in accordance with § 14.



4. supervision of the notified body



4.1. The purpose of surveillance is to make sure that the installer duly fulfils the obligations

arising out of the approved quality system.



4.2 the supplier shall allow the notified body in order to assess access to

the space intended for the installation, inspection and testing locations and provide it

all necessary information, in particular



and quality system documentation)



(b)) the technical documentation, and



(c)) the quality records, such as inspection reports and records from the

tests carried out, records of the performed calibration,

the qualifications of the personnel concerned, etc.



4.3. the notified body shall carry out periodic audits to make sure that

the installer maintains and applies the quality system and shall provide the installer

an audit report.



4.4. Additionally, the notified body may make unannounced inspection

visit to the place of installation of the lift.



During such visits the notified body may, if necessary,

or have carried out tests to verify that the quality system and the lift properly

they work. The notified body shall provide the supplier with a visit report and

the Protocol, if they have been carried out.




5. the supplier shall keep at the disposal of the supervisory authority for a period of 10 years from the

the last of the lift on the market



and the documentation referred to in point), 3.1 (b). (c)),



(b)) the technical documentation referred to in point 3.1 (b). (d)),



c) information about the change referred to in point 3.4.1 and



(d)) the conclusions and reports of the notified body which are referred to in

3.4.2, points 4.3 and 4.4.



6. each notified body shall inform the authority of certificates of approval

quality system issued or withdrawn, and shall, periodically or upon request,

the Office shall make available a list of the approval certificate, which it has refused

, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

certificates of quality system approvals which it has refused

suspended or withdrawn, and, on request, about certificates of approval

It has issued.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of quality system approval

It has issued.



7. CE marking and EU Declaration of conformity



7.1 the supplier shall affix in a cage of each lift, which meets the basic

the technical requirements of the CE marking, and placed next to the CE marking in the cage

each lift the identification number of the notified body referred to in point 3.1.



7.2 the supplier shall draw up a written EU Declaration of conformity for each elevator and

a copy of the EU Declaration of conformity shall keep at the disposal of the supervisory authority for

10 years after the lift on the market. A copy of the EU Declaration of conformity

the request shall provide the supervisory authority.



8. Authorized Representative



Supplier's activities set out in points 3.1, 3.4.1, 5 and 7 may be his

behalf and under his responsibility fulfilled by his authorised representative,

If the manufacturer's authorised representative established in the mandate.



Č. 11



CONFORMITY BASED ON FULL QUALITY ASSURANCE PLUS DESIGN EXAMINATION

WHEN IT COMES TO ELEVATORS



(module H1)



1. conformity based on full quality assurance plus design examination

in terms of lifts, it is the conformity assessment procedure whereby a notified

It assesses the quality system of the supplier and, where appropriate, a proposal from the lifts with the

to ensure that the lifts comply with the relevant technical background

requirements.



2. the activities of the supplier



The supplier shall operate an approved quality system for design, manufacture,

mounting, installation, final lift inspection and testing as specified in point 3 and

shall be subject to surveillance as specified in point 4. The adequacy of the technical design of the lifts

must be reviewed in accordance with section 3.3.



3. quality system



3.1 the supplier shall submit with a single notified body of his choice,

application for assessment of his quality system.



The application must include



and the name and address of the supplier), and if the application is lodged by the authorized

Representative, his name and address,



(b)) all relevant information on the lifts, which are to be

installed, in particular information which makes for an understanding of the relationship

between the design and operation of the lift,



(c) quality system documentation)



(d)) the technical documentation described in point 3 of part B of the annex No 4 to

of this regulation and



e) a written declaration that the same application has not been lodged with any other

of the notified body.



3.2. The quality system shall ensure compliance of the lifts with the relevant

basic technical requirements. All the elements, requirements, and

provisions adopted by the installer must be systematic and orderly

documented in the form of written measures, procedures and instructions. This

the quality system documentation must permit a consistent interpretation of the procedures,

for example, programmes, plans, manuals and records relating to quality.



This quality system documentation shall contain in particular an adequate description of the



and) the objectives in terms of quality and the organisational structure, responsibilities and

powers of the management with regard to design and product quality,



(b)) the technical design specifications, including standards, that will be used, and

in the case that the relevant harmonised standards shall not be used in full

the scope, the means, including other relevant technical

specifications, that will be used to ensure that the

the essential technical requirements,



c) inspection and design verification techniques, processes and systematic

the activities that will be used when designing the lifts,



(d)) the examinations and tests that will be carried out when taking delivery

materials, components and sub-assemblies,



(e)) of the respective techniques, processes and systematic actions that are

be used for the Assembly, installation, inspection and quality assurance techniques,



f) examinations and tests that will be carried out before installation

(for example, inspection of installation conditions: shaft, housing of machinery), during

installation and after installation (including at least the tests referred to in point 3.3.

Annex 5 to this Regulation),



(g)) the quality records, such as inspection reports and records of the

tests carried out, records of calibration reports

the qualifications of the staff concerned, and



h) the means of monitoring the achievement of the required quality

the design and the product and the efficient operation of the quality system.



3.3 design review



3.3.1 if the design is not entirely in accordance with harmonized standards,

a notified body finds that the design meets the basic technical

requirements, and if so, issues a certificate to the supplier of the EU

examination of the design with the indication of the limits of validity of the certificate and the data

necessary for identification of the approved design.



3.3.2 If the design does not satisfy the relevant technical requirements,

the notified body refuses to issue EU design examination certificate and

It shall inform the supplier, with the refusal of the refusal.



The notified body shall ensure that it is kept informed of any changes in the generally

acknowledged State of the art which indicate that the approved design no longer

may not be in accordance with the basic technical requirements, and decides

whether such changes require further investigation. If the investigation so require,

the notified body shall inform the supplier.



3.3.3. The contractor shall inform the notified body that has issued certificate of EU

examination of the design of all modifications to the approved design that may have

affect the conformity with the essential requirements or the conditions

the validity of the certificate. Such a change of the notified body which issued the

EU design examination certificate, in the form of an appendix to approve additional

the original EU design examination certificate.



3.3.4. Each notified body shall inform the authority of EU certificates

design review and any additions thereto which it has issued or withdrawn, and

shall, periodically or upon request, make available to the authority the list of EU certificates

design review and any additions thereto which it has refused, suspended or otherwise

restricted.



Each notified body shall inform the other notified bodies of the

EU design examination certificates and/or any additions thereto which it has refused,

withdrawn, suspended or otherwise restricted, and, upon request, about the certificates and

additions thereto which it has issued.



The European Commission and European Union Member States and the other notified

operators may request the notified body for a copy of the certificate of the EU

a review of the proposal and the amendments to them. The European Commission and the Member States

The European Union may apply to the notified body for a copy of the technical

documentation and the results of the review carried out by the notified body.



3.3.5 the vendor keeps a copy of EU design examination certificate, its

annexes and additions together with the technical documentation at the disposal of the authority

supervision for a period of 10 years after the lift on the market.



3.4 Assessment of the quality system



The notified body shall assess the quality system to determine whether it satisfies

the requirements referred to in 3.2. The elements of the quality system that conform to the

the relevant specifications of the relevant harmonised standards, compliance with these

the requirements of the standard.



In the auditing team must have at least one member with experience of

the elevator technology assessment techniques and knowledge of the basic

technical requirements. The audit includes an assessment visit to the premises of the

the premises of the supplier and on the place of installation of the lift.



Auditing team shall review the technical documentation referred to in point 3.1.

(a). (d)), in order to verify that the supplier is able to determine the appropriate base

technical requirements and carry out the necessary review to ensure

compliance with these requirements in respect of the lift.



The conclusions of the audit, including justification shall notify the supplier, or

his authorised representative.



3.5 the supplier undertakes to fulfil the obligations arising out of the

quality system as approved and to maintain it so that it remains

adequate and efficient.



The supplier shall inform the notified body that has approved the quality system,

any intended change to the system.



The notified body must assess the changes proposed and decide whether the modified

the quality system will still satisfy the requirements referred to in point 3.2,

or whether a re-assessment is necessary.



The notified body shall notify the supplier, where applicable, his authorised

the representatives, including its assessment of the conclusions of their justification.



The notified body shall affix, or cause to be positioned next to the CE marking of your

identification number in accordance with § 14.



4. supervision of the notified body



4.1. The purpose of surveillance is to make sure that the installer duly fulfils the obligations

arising out of the approved quality system.



4.2 the supplier shall allow the notified body in order to assess access to


the places of design, manufacture, Assembly, installation, inspection and

testing and storage and shall provide it with all necessary information, in particular



and quality system documentation)



(b)) the quality records provided for in part of the quality system relating to

the design, such as results of analyses, calculations, tests, and



(c)) the quality records provided for in part of the quality system relating to

taking delivery and installation, for example, reports of inspections,

the records of the tests carried out, records of the performed calibration, news

about the qualifications of the staff concerned.



4.3. the notified body shall carry out periodic audits to make sure that

the installer maintains and applies the quality system and shall provide the installer

an audit report.



4.4. Additionally, the notified body may make unannounced inspection

visit the supplier's premises or at the place of installation

the elevator. During such visits the notified body may, if necessary,

carry out or have carried out tests to verify that the quality system is properly

works. The notified body shall provide the supplier with a visit report and

the Protocol, if they have been carried out.



5. the supplier shall keep at the disposal of the supervisory authority for a period of 10 years from the

placing on the market



and the documentation referred to in point), 3.1 (b). (c)),



(b)) the technical documentation referred to in point 3.1 (b). (d)),



c) information about the change referred to in point 3.5 and the



(d)) the conclusions and reports of the notified body referred to in points 3.5,

4.3 and 4.4.



6. each notified body shall inform the authority of certificates of approval

quality system issued or withdrawn, and shall, periodically or upon request,

the Office shall make available a list of certificate of quality system approval

refused, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

certificates of quality system approvals which it has refused

suspended or withdrawn, and, on request, about certificates of approval system

the quality which it has issued.



The notified body shall keep a copy of the approval certificate, which it has issued,

its annexes and additions, as well as the technical documentation for a period of

15 years from the date of their issue.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of quality system approval

It has issued.



7. CE marking and EU Declaration of conformity



7.1 the supplier shall affix in a cage of each lift, which meets the basic

the technical requirements of the CE marking, and placed next to the CE marking in the cage

each lift the identification number of the notified body referred to in point 3.1.



7.2 the supplier shall draw up a written EU Declaration of conformity for each elevator and

a copy of the EU Declaration of conformity shall keep at the disposal of the supervisory authority for

10 years after the lift on the market. A copy of the EU Declaration of conformity

the request shall provide the supervisory authority.



8. Authorized Representative



Supplier's activities set out in points 3.1, 3.3.5, 3.3.3, 5 and 7 may

be on his behalf and under his responsibility fulfilled by his authorised

Representative, if the authorised representative of the manufacturer in the credential

It has specified.



Č. 12



CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTION, AS REGARDS

LIFTS



(module D)



1. conformity to type based on quality assurance of the production, as regards

lifts, is the part of a conformity assessment procedure, the notified body

assesses the quality of the production system supplier with the aim to ensure that

the lifts were installed in conformity with the approved type as described in the

the EU type-examination certificate or with an elevator designed and manufactured in

part of the quality system approved in accordance with Annex 11 to this

Regulation and comply with the relevant basic technical requirements.



2. the activities of the supplier



The supplier shall operate an approved quality system for production, installation,

installation, final lift inspection and testing as specified in point 3 and shall be subject to

surveillance as specified in point 4.



3. quality system



3.1 the supplier shall submit with a single notified body of his choice,

application for assessment of his quality system.



The application must include



and the name and address of the supplier), and if the application is lodged by the authorized

Representative, his name and address,



(b)) all relevant information on the lifts, which are to be

installed,



(c) quality system documentation)



(d)) the technical documentation of lifts which are to be installed, and



e) a written declaration that the same application has not been lodged with any other

of the notified body.



3.2. The quality system shall ensure compliance of the lifts with the relevant

basic technical requirements.



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

a systematic and orderly manner in the form of written policies,

procedures and instructions. This quality system documentation must permit a consistent

interpretation programmes, plans, manuals and records relating to quality.



Production quality system documentation shall contain in particular an adequate

Description



and) the objectives in terms of quality and the organisational structure, responsibilities and

powers of the management with regard to product quality,



(b)) techniques, processes and systematic actions that will be used when

production, control and quality assurance,



(c)) the examination and tests that will be carried out before the installation, during the

installation and after installation,



d) quality records, such as inspection reports and records of the

tests carried out, records of calibration reports

the qualifications of the personnel concerned, and



(e)) the means of monitoring the achievement of the required quality

products and the efficient operation of the quality system.



3.3 the notified body shall assess the quality system to determine whether it satisfies

the requirements referred to in 3.2. The elements of the quality system that conform to the

the relevant specifications of the relevant harmonised standards, compliance with these

the requirements of the standard.



In the auditing team must have at least one member with experience of

the elevator technology assessment techniques and knowledge of the basic

technical requirements.



The audit includes an assessment visit to the premises of the supplier and

on the place of installation of the lift.



The conclusions of the audit, including the reasons therefor shall be notified to the supplier.



3.4 the supplier shall undertake to fulfil the obligations arising from the

the quality system as approved and to maintain it so that it

remains adequate and efficient.



3.4.1. The contractor shall inform the notified body that has approved the system

the quality of any intended change to the system.



3.4.2. The notified body must assess the changes proposed and decide whether the modified

the quality system will still satisfy the requirements referred to in point 3.2,

or whether a re-assessment is necessary.



The notified body shall notify the supplier of the conclusions of its assessment, including their

justification.



The notified body shall affix, or cause to be positioned next to the CE marking of your

identification number in accordance with § 14.



4. supervision of the notified body



4.1. The purpose of surveillance is to make sure that the installer duly fulfils the obligations

arising out of the approved quality system.



4.2 the supplier shall allow the notified body in order to assess access to

the space intended for the manufacture, Assembly, installation, inspection, testing and

storage and must provide it with all necessary information, in particular



and quality system documentation)



(b)) the technical documentation, and



(c)) the quality records, such as inspection reports and records from the

tests carried out, records of the performed calibration,

the qualifications of the staff concerned.



4.3. the notified body shall carry out periodic audits to make sure that

the installer maintains and applies the quality system and shall provide the installer

an audit report.



4.4. Additionally, the notified body may take place at the supplier unannounced

visits. During such visits the notified body may

If necessary, carry out or have carried out tests to verify that the

the quality system is functioning correctly. The notified body shall provide to the supplier

with a visit report and, if tests have been carried out.



5. the supplier shall keep at the disposal of the supervisory authority for a period of 10 years from the

placing on the market



and the documentation referred to in point), 3.1 (b). (c)),



(b)) the technical documentation referred to in point 3.1 (b). (d)),



c) information about the change referred to in point 3.4.1 and



(d)) decisions and reports of the notified body referred to in points

3.4.2, 4.3 and 4.4.



6. each notified body shall inform the authority of certificates of approval

quality system issued or withdrawn, and shall, periodically or upon request,

the Office shall make available a list of certificate of quality system approval

It has refused, suspended or otherwise restricted.



Each notified body shall inform the other notified bodies of the

certificates of quality system approvals which it has refused

suspended or withdrawn, and, on request, about certificates of approval system

the quality which it has issued.



The notified body shall provide to the European Commission and the Member States of the European

the Union at the request of a copy of the certificate of quality system approval

It has issued.



7. CE marking and EU Declaration of conformity



7.1 the supplier shall affix in a cage of each lift, which meets the basic

the technical requirements of the CE marking, and placed next to the CE marking in the cage

each lift the identification number of the notified body referred to in point 3.1.




7.2 the supplier shall draw up a written EU Declaration of conformity for each elevator and

a copy of the EU Declaration of conformity shall keep at the disposal of the supervisory authority for

10 years after the lift on the market. A copy of the EU Declaration of conformity

the request shall provide the supervisory authority.



8. Authorized Representative



Supplier's activities set out in points 3.1, 3.4.1, 5 and 7 may be his

behalf and under his responsibility fulfilled by his authorised representative,

If the manufacturer's authorised representative established in the mandate.



1) directive of the European Parliament and of the Council of the EU of 33/26. February

2014 on the harmonisation of the laws of the Member States relating to the

lifts and safety components for lifts.