27/2003 Coll.
REGULATION OF THE GOVERNMENT
of 9 June. December 2002, laying down the technical requirements for
lifts
Change: 127/2004 Sb.
Change: 142/2008 Sb.
The Government ordered pursuant to section 22 of Act No. 22/1997 Coll., on technical
requirements for products and amending and supplementing certain acts, as amended by
Law No 71/2000 Coll. and Act No. 205/2002 Coll. (hereinafter the "Act") to
the implementation of § 11 (1). 2, § 11a paragraph. 2 (a). (c)), section 12 paragraph. 1 and 3 and section 13
paragraph. 2 of the Act:
§ 1
Basic provisions
(1) this regulation in accordance with the law of the European Communities ^ 1)
provides technical requirements for lifts which permanently serve different
altitude levels of buildings and constructions, and on the security components that are
intended for the use of these lifts.
(2) for the purposes of this regulation, the lift shall mean a lifting device
serving various height levels, having a carrier moving between
guides which are rigid and inclined at an angle of more horizontal
than 15 °, intended for the carriage of
and) persons
(b)) of persons and goods,
(c)) goods alone if the carrier is accessible so that it can be used without
difficulties to enter, and it is fitted with the control device on the carrier, or
within easy reach of the person, which is located on it.
For elevators pursuant to this regulation and shall be regarded as lifting devices,
the carrier does not move between fixed guides if they have
the specified path of the movement.
(3) this Regulation shall not apply to
and) lifting equipment, whose speed does not exceed 0.15 m/s,
(b) construction site hoists),
(c)), including the funicular funicular railways,
d) lifts specially designed and constructed for military or police
purposes,
e) lifting equipment intended to make were carried out the work,
f) mining equipment
g) lifting appliances intended for lifting performers
during the performance,
h) lifting equipment in vehicles,
I) lifting appliances connected to machinery and intended exclusively for
ensure access to workstations including maintenance and control of the
the machinery,
j) COG railways,
k) escalators and moving walkways.
(4) for the purposes of this Regulation shall mean:
and the lift manufacturer) natural or legal person who, by sought
the CE marking on the lift, assumes responsibility for the design, manufacture, Assembly,
and placing on the market and which issues the EC declaration of conformity (hereinafter referred to as
"the lift"),
(b) the manufacturer of the safety components) of the natural or legal person,
who is responsible for the design and manufacture of the safety components and
affixes the CE marking on the safety component and that are issued by EC
the Declaration of conformity,
(c) a component part of) the security referred to in the list in annex 4 to
of this regulation,
(d)) of the lift elevator, for which the technical documentation demonstrating
the technical requirements will be met for lifts from the model
the elevator, which uses identical safety components and
Specifies all of the permissible differences between the lift and hoists
derived from the model lift, indicating the maximum and minimum
values. Is allowed to show by calculation or design drawings
the similarity of the type series of lifts, to demonstrate how they have been complied with
the basic safety requirements laid down by this regulation,
(e) the placing on the market), the moment when a vendor passes for the first time
the user to use the elevator,
f) carrier of that part of the elevator, which are carried by persons or cargo
When lifting or lowering.
(5) the technical requirement for elevators, which is completely or partially
contained in another government regulation, this other government regulation.
(6) laid down the products under this regulation within the meaning of section 12, paragraph. 1
(a). and there are lifts and) of the safety components.
§ 2
Conditions for the placing of lifts and safety components on the market and putting into service
(1) on the market and put into service may be listed
and) lifts under the condition that does not cause a risk to the health and safety of persons
or property, provided that they are properly installed, maintained and
used in accordance with the intended purpose,
(b)) of the safety component, provided that the lifts in which they are to be
used does not cause a threat to the health and safety of persons or property, for
provided that they are properly installed, maintained and used in the
accordance with the intended purpose.
(2) Elevators shall comply with the technical requirements relating to the protection of the health
and the security referred to in annex 1 to this Regulation (hereinafter referred to as
"essential requirements").
(3) safety components must meet the basic requirements for
health and safety referred to in annex No. 1 or
enable the lifts in which they are mounted, to meet the essential
the requirements.
(4) the installer of a lift must provide the necessary information to the person responsible
for the construction work on the relevant construction (building) and in conjunction with this
the person take the necessary steps to allow the proper operation and safe
the use of the elevator.
(5) the Lift must not be placed into the shafts, in which are located the pipeline,
electrical installations or facilities which are not necessary for the operation and
safety of the lift.
(6) the lifts or safety components which do not satisfy the requirements of
of this regulation, may be presented or exhibited at trade fairs,
exhibitions or demonstrations only when visible inscription on this
the fact draws attention. These products may not be sold, given the
the market and/or put into service until they have been given a lift by the supplier, or
the manufacturer of the safety component or his authorized representative in the
accordance with this regulation. During the demonstrations must be being
taken the appropriate security measures to ensure the
the protection of persons.
(7) any lift or safety component which meet all
the requirements of this regulation, including the conformity assessment procedures shall be
before being placed on the market after the conformity according to § 3 of the CE marking
and equipped with EC declaration of conformity referred to in annex 2 to this regulation,
taking into account, as appropriate, in the case of safety components
Annex No. 8, 9 or 11 of this regulation and annex No 6 lifts, 10,
12, 13 or 14 of this regulation.
(8) the essential requirements shall be considered satisfied if the elevator or
safety component in conformity
and with the harmonised Czech) technical standards, where appropriate,
foreign technical standards incorporating in the Member States
The European Union harmonised European standards (Section 4a of the Act), or
(b)) in the case that, in the relevant areas of technical standards referred to in point (a))
There are, with specified standards (Section 4a of the Act), including the Czech or
foreign technical standards, which were announced by the Commission for this purpose
Of the European Communities (hereinafter referred to as "the Commission").
§ 3
Conformity assessment procedures
(1) prior to the placing on the market of safety components provided by the manufacturer
the safety components or his authorized representative an assessment
matches any one of the following procedures (article 12, paragraph 4, of the Act) in accordance with its
options
and the type-examination of safety components) under part A of the annex No 5
to this regulation and an assessment of the conformity of the safety components with the
● the type of spot check in accordance with Annex 11 to this
Regulation,
(b)) the type-examination of safety components referred to in part A of the annex No 5
to this regulation and quality assurance procedure security
components referred to in annex 8 to this regulation, or
(c) the comprehensive quality assurance) of the safety components referred to in
Annex 9 to this regulation.
(2) prior to the placing of lifts on the market provides an assessment of the lift
matches any one of the following procedures (article 12, paragraph 4, of the Act) in accordance with its
options
and the same with the lift) lift, which was subjected to an EC type-examination
lift in accordance with part B of annex 5 to this regulation, are in the production stage,
the installation and testing of the lift shall examine the conformity of
1. the final inspection referred to in annex 6 to this regulation,
2. quality assurance referred to in annex 12 to this regulation,
or
3. production quality assurance for lifts specified in annex 14 to this
of the regulation.
The conformity assessment procedures related to how to design and manufacture, so to
installation and testing of the lift may be carried out on the same elevator,
(b)) at the elevator in conformity with the model lift having undergone an EC
type-examination of the lift in accordance with part B of annex 5 to this regulation,
at the stage of manufacture, Assembly and testing of the lift shall examine the conformity of
1. the final inspection referred to in annex 6 to this regulation,
2. quality assurance referred to in annex 12 to this regulation,
or
3. production quality assurance for lifts specified in annex 14 to this
Regulation,
(c)) at the elevator in the same elevator, for which application of the procedure
quality assurance in accordance with annex 13 to this
Regulation supplemented by checking the design, if the design is not entirely in the
accordance with harmonised standards, is at the stage of manufacture, Assembly and
In addition, testing assesses the conformity of the lift
1. the final inspection referred to in annex 6 to this regulation,
2. quality assurance referred to in annex 12 to this regulation,
or
3. production quality assurance for lifts specified in annex 14 to this
Regulation,
(d) the verification of the conformity of each elevator) as defined in annex 10 to this
Regulation, or
(e) a comprehensive quality assurance) in accordance with annex 13 to this
Regulation supplemented by checking the design, if the design is not entirely in the
accordance with harmonised standards.
(3) in the cases referred to in paragraph 2 (a). and (b))) and (c)), the person
responsible for the construction of the disposal of the person responsible for the manufacture,
Assembly and testing of all the documents and information necessary for the implementation of
These activities.
(4) evidence of conformity assessment (section 13 paragraph 7 of the Act) include a copy of the EC
the Declaration of conformity and the documents, which, depending on the procedure
conformity assessment are listed in the corresponding provisions of the annexes to the
of this regulation.
(5) the Commission of the European communities, the Member States of the European Union and
the competent notified person ^ 2) may receive on request from a supplier
Elevator, a copy of the EC declaration of conformity and the report on the tests conducted in
final inspection.
(6) If neither the installer of the lift nor the manufacturer of the safety components,
or his authorised representative fulfils the obligations laid down in paragraphs 1
up to 5, these obligations are met, everyone who places the lift or safety
component on the market. These obligations shall apply to whomsoever manufactures lift
or safety component for their own use.
§ 4
The CE marking and other labelling
(1) the CE marking, whose graphic design provides for special legal
prescription, ^ 3) must be stated clearly in each elevator cage and
visibly in accordance with point 5 of annex 1 to this regulation and all
safety components or, if not possible, on a label
inseparably attached to the safety component. Minimum dimension
marking of 5 mm may be waived for small-scale safety components.
(2) For the CE marking must bear the identification number of the notified
persons involved in the procedures referred to in section 3, paragraph 3. 1 or 2. On
the lift or safety component may be fitted to any other
marking provided that the visibility and legibility of the CE marking, the
will not diminish.
(3) the lift or safety component shall not bear the designation,
that could mislead anyone regarding the CE marking.
(4) the CE marking on the lifts or safety components,
that the product meets the technical requirements laid down in any legal
the provisions which apply to it and that this marking set
or allow, and that was followed in the assessment of its conformity provided for
the procedure. However, if one or several of the legislation after
transitional period, admits to the lift or the manufacturer of the
safety components, to choose which provisions will govern,
CE marking shall indicate conformity only with those laws or
their provisions, which the lift or the manufacturer of the safety
the components used. In this case, it must be in the documentation, notices
or instructions required by the legislation concerned and annexed to the
the relevant products, information on the relevant legislation
Of the European communities or of their provisions, which the supplier
the lift or the manufacturer of the safety components used.
§ 5
Notice of the imposition of protective measures
In the event that it was for the lift or safety component is saved
protective measures under special legislation, ^ 4) shall be in the
notification of the decision on the imposition of a safeguard measure pursuant to § 7 (2). 8
the law, whether the non-compliance was caused by
and satisfy the essential requirements),
(b) incorrect application of technical standards) referred to in section 2 (2). 7,
c) shortcomings in the technical standards referred to in section 2 (2). 7.
§ 6
The conditions of the authorization
(1) the authorization of legal entities under section 11 (2). 2 of the Act
apply the conditions of the authorization referred to in annex 7 to this regulation.
Legal entities which meet the criteria laid down in the relevant
harmonised standards shall be regarded as satisfactory by the competent
conditions.
(2) an authorized person, the procedure laid down in section 11 (1). 7 of the law becomes
by the person.
Transitional and final provisions
section 7 of the
(1) valid certificates or other documents issued on the basis of regulation
No 14/1999 Coll., as amended by regulation of the Government No. 227/1999 Coll. and
Government Regulation No 288/2000 Coll., may be used for the purposes of assessing the
conformity in accordance with this regulation, unless they are cancelled under the conditions
laid down by law.
(2) the person responsible for the activities of conformity assessment pursuant to Regulation
No 14/1999 Coll., as amended by regulation of the Government No. 227/1999 Coll. and
Government Regulation No 288/2000 Coll., shall be deemed to obtain by
of this regulation.
§ 8
Shall be repealed:
1. Government Regulation No. 14/1999 Coll., laying down technical requirements
on the lifts.
2. Government Regulation No. 227/1999 Coll., amending Decree-Law No.
14/1999 Coll., laying down technical requirements for elevators.
3. Government Regulation No 288/2000 Coll., amending Decree-Law No.
14/1999 Coll., laying down technical requirements for elevators in the text of the
Regulation of the Government No. 227/1999 Sb.
§ 9
The effectiveness of the
This Regulation shall enter into force on the date of entry of the Treaty of accession of the Czech
Republic to the European Union.
The President of the Government:
PhDr. Spidla in r.
Minister of industry and trade:
Ing. Samantha r in r.
Annex 1
THE BASIC REQUIREMENTS FOR THE PROTECTION OF HEALTH AND SAFETY, RELATING TO THE
DESIGN AND CONSTRUCTION OF LIFTS AND SAFETY COMPONENTS
INTRODUCTORY PROVISIONS
1. basic requirements to the lifts or safety components
apply only if you use the lift or safety
the components under the conditions specified by the supplier of the lift or the manufacturer
safety components can give rise to the risk that
basic requirements apply. The possibility of the risk of the lift
or the manufacturer of the safety components in advance analyses, evaluates and
ensures production with regard to this analysis.
2. If you cannot achieve at the current state of the art fully the purpose for
which were laid down in the essential requirements, it is necessary to lift
or the manufacturer of the safety components to care to ensure the security of
to the extent the most approaching the essential requirements.
1.
GENERALLY
1.1 the use of the regulation of the Government No. 24/2003 Coll., laying down the technical
requirements for machinery (hereinafter "Decree-Law No 24/2003
SB. ").
If there is a corresponding danger and is not mentioned in this annex,
the requirements for the protection of the health and safety referred to in annex No. 2
to the regulation of the Government No. 24/2003 Coll., Basic requirements of Annex No. 2 point
1.1.2. Regulation of the Government No. 24/2003 Coll. must apply in each
case. The elevators are also covered by the essential requirements referred to in
a special law, which sets out the technical requirements for
building products called CE, ^ 4a) if in this Government Regulation
set are not. As regards aspects relating to the installation of the lifts,
If they are satisfied the requirements laid down by this regulation, shall be deemed
fulfilled the requirements laid down in a special legal regulation, which
technical requirements for construction products called CE ^ 4a)
1.2 carrier
The carrier must be caged. This car must be designed and
so constructed that its space and strength match supplier
be determined by the maximum number of persons and the load capacity of the lift.
If dimensions permit, the car must be in the case of lifts intended for
the transport of persons, designed and constructed so that its construction
features do not obstruct or impede access and use by persons with reduced
mobility, for example, persons in wheelchairs,
and to allow any appropriate adjustments that these persons may
to facilitate its use.
1.3 Suspension and support equipment
Pendant or device, the support car, its fastening and
the connecting parts must be designed and selected to ensure that the
the necessary level of safety and to minimise the risk of falling,
taking into account the conditions of use, the materials used and the production
the conditions.
Where to hang the cages, ropes or chains must be used
at least two independent ropes or chains, each with a separate
fastening. Ropes and chains must not be set if it is not necessary to
for mounting or to create the ok.
1.4. control of loading (including overspeed)
1.4.1. Lifts must be so designed, constructed and installed so that in the
the event exceeded set by the elevator was prevented from
putting them 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 drive
prevents overspeed.
1.4.3. Fast lifts must be equipped with checkers 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 machinery
1.5.1 all passenger lifts must have their own individual lift machinery. This
requirement does not apply to lifts in which the balancing weights
replaced the second cage.
1.5.2. the installer of the lift must ensure that the lift machinery and the
belonging to the device are not accessible except for maintenance and emergency
cases.
1.6 Control
1.6.1. The controls of lifts intended for persons with restricted mobility
motion and orientation must be suitably constructed and fitted.
1.6.2 Function controls must be clearly marked.
1.6.3 the call circuits of a group of lifts may be common or
linked.
1.6.4. Electrical equipment must be installed and connected to
and) was no possible confusion with circuits which do not relate to the elevator;
(b) it was possible to switch off the power) under load;
(c)) was perhaps the only elevator ride in the proper operation of the safety
devices in a separate electrical (control)
safety circuit;
d) fault in the electrical installation was not the cause of the dangerous
the situation.
2.
HAZARDS 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
normal use of the elevator.
2.2. The lift must be designed and constructed so as to prevent the risk of
the grip of the persons, if the car is in one of its extreme positions.
This requirement is met by an open space or escape in the
the area of the end positions.
Whereas, in special cases, in particular in the existing
buildings is not possible, said the solution may 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
the door must have for the intended operating conditions corresponding to the
mechanical resistance.
The 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,
(b)) the opening of a landing door when the car is still moving and outside a
the designated landing zone.
It is, however, permitted to commute with the doors open in a particular zone for
provided that the speed is controlled by the dojížděcí.
3.
THE DANGER FOR PERSONS IN THE CAGE
3.1 lift cars must be completely enclosed by full-length walls, full height
including the floor and ceiling, with the exception of ventilation apertures, and with full-length
the door. These doors must be so designed and installed as to cage
She couldn't move, unless the doors are closed, with the exception of commuting
referred to in the last sentence of paragraph 2.3, and stopped, if the doors are
the open.
The cage door must 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
the elevator the elevator must be equipped with devices to prevent free falling
or uncontrolled upward movements of the cage.
The device to prevent free falling of the cage must not be dependent on hinge
the cage.
This device must be capable of stopping the cage at the load corresponding to the
load and at the maximum speed set by the elevator. When
any load must stop this device to cause dangerous
the slowdown for transported persons.
3.3 between the bottom of the shaft and the floor of the cage must be placed
the 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 the cage due to
the construction of the propulsion system can not get to the free space referred to in
2.2.
3.4. Lifts must be so designed and constructed as to make it possible
set in motion if the device provided for in section 3.2 is not in
stand-by position.
4.
OTHER HAZARDS
4.1 the landing doors and car doors or the two doors together, where
motorized, must have a device to prevent the moving door.
4.2. landing doors are to contribute to the protection of the building against the spread
fire, including its glass parts, must have an appropriate
fire resistance, in terms of their integrity, insulation properties
(containment of flames) and radiation (heat flow density). If the
all landing doors, including those with glass parts, serve to protect the
the building against fire, must be suitably resistant to fire, as regards
their integrity and their properties (resistance to flames) and the
transmission of heat (thermal radiation).
4.3. Counterweights must be so installed as to 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. cars must be fitted with two-way means of
allowing connection to a permanent rescue service.
4.6. Lifts must be so designed and constructed so that they can complete
ride in the event that the temperature in the lift machine exceeding the
the maximum set by the elevator, but that did not respond to other
the commands.
4.7. cars must be designed and constructed so that for
transported the person to ensure sufficient ventilation, and even in the case of
a prolonged stoppage.
4.8. The car should be adequately lit whenever
filled, or a door is opened; the cage must also have emergency
lighting.
4.9. the device 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
the normal power supply. The duration of their function must be long enough
to allow the normal rescue procedure.
4.10 Control circuits of lifts which may be used in case of fire,
(fire or evacuation elevators) must be designed and constructed
to prevent stopping the elevator at set levels and allow
priority management of the lift by rescue teams.
5.
MARKING
5.1 in addition to the minimum information required for all machinery
in accordance with point 1.7.3 of annex 2 to the regulation of the Government No. 24/2003 Coll., shall be
each cage equipped with a clearly visible label clearly show the
load in kilograms and the maximum number of passengers who can
be transported.
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 in
Czech language clearly and visibly placed in the cage.
6.
INSTRUCTIONS FOR USE
6.1 the safety components listed in annex 4 to this regulation,
must be provided with a manual drawn up in the Czech language and, where appropriate,
in a language that the person notified by the manufacturer agrees with the safety
components or his authorised representative to
and Assembly)
(b)),
(c)),
(d)) maintenance
they can be carried out correctly and without danger.
6.2 each lift must be equipped with the documentation drawn up in the Czech,
language and, where appropriate, also in the language of the community which may be determined by the
European Union Member State in which the lift is installed.
The documentation contains at least
and) instructions for use, including the drawings and diagrams necessary for normal
operation of and relating to maintenance, inspection, repair, periodic
checks and the rescue operations referred to in point 2.7;
(b)) a logbook in which repairs are recorded, regular checks
and the like.
Annex 2
1.
CONTENTS OF THE EC DECLARATION OF CONFORMITY FOR SAFETY COMPONENTS
EC declaration of conformity must contain the following information:
and manufacturer identification data) of the safety components,
(b)) the identity of the authorized representative, if established,
(c) a description of the safety component), the designation of type or series and serial
number, if any,
(d)) the safety features of the safety component, if not obvious from the
Description
(e)) the year of manufacture of the safety component,
f) all relevant provisions to which the safety component complies,
g) links to the technical standards referred to in § 2, if used,
h) identification of the notified person, if conducted by EC
type-examination pursuant to § 3 (2). 1,
I) link to the EC type-examination certificate, if issued,
j) identification data notified to the person, if you inspect
production according to § 3 (2). 1,
to obtain identification data) to the person, if the referee system
quality assurance provided by the manufacturer of the safety components
According to § 3 (2). 1,
l) signed by a person authorized to act on behalf of the manufacturer
safety components or of its authorized representatives.
The Declaration of conformity must be written on a typewriter or in block letters in the
the same language as the instruction manual referred to in point 6.1 of Annex No. 1 to the
of this regulation.
2.
THE CONTENTS OF THE DECLARATION OF CONFORMITY FOR INSTALLED LIFTS
The Declaration of conformity must contain the following information:
and the identification of the supplier) of the lift,
(b)), the type description of the lift, or series, serial number and the address where
the lift is fitted,
(c) the year of installation of the lift,)
(d)) all relevant provisions to which the lift conforms,
e) link to the technical standards referred to in § 2, if used,
f) identification of the notified person, if conducted by EC
type-examination of the model of the lift in accordance with § 3 (1). 2,
g) link to the EC type-examination certificate, if issued,
h) identification of the notified person, if carried out verification
the conformity of the lift in accordance with § 3 (1). 2,
I) identification data notified to the person, if carried out the final
inspection of the lift in accordance with § 3 (1). 2,
j) identification data notified to the person, if the referee system
quality assurance provided by the supplier according to § 3 (2). 2,
signed to) data on the person authorized to act on behalf of or on behalf of
the lift.
The Declaration of conformity must be written on a typewriter or in block letters in the
the same language as the instruction manual referred to in section 6.2 of Annex No. 1 to the
of this regulation.
Annex 3
THE CE MARKING
The graphic form of the CE marking is laid down specific legal
Regulation ^ 3), unless otherwise specified.
The minimum dimension of 5 mm may be waived for small-scale safety
components.
For the CE conformity marking shown identification number of the notified
the person who deals with
and procedures set out in section) 3 (3). 1,
(b) the procedures referred to in section) 3 (3). 2.
Annex 4
THE LIST OF SAFETY COMPONENTS
1. Devices for locking landing doors.
2. the device referred to in point 3.2 of annex 1 to this regulation, which
prevent you from falling or unchecked upward movements.
3. the device to prevent excessive speed.
4A. the energy-accumulating shock absorbers
-either non-linear,
-or with damping of the return movement.
4B. the energy-dissipating shock absorbers.
5. Safety devices hydraulic cylinder hydraulic
the circuit used as devices to prevent falls.
6. Electric safety devices the safety represented by the
switches with electronic components.
Annex 5
EC TYPE-EXAMINATION
(Conformity assessment procedure (B))
And the.
EC TYPE-EXAMINATION OF SAFETY COMPONENTS
1. EC type-examination (hereinafter referred to as "type-examination") security
the component is the procedure whereby a notified body ascertains and certifies
a sample of the safety component allows the lift, in which the
safety component correctly correctly fitted to satisfy the essential
the requirements.
2. the manufacturer of the safety component or his authorized representative
provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the details of the place of manufacture of the safety component,
(b)) a written declaration that the Treaty was not to carry out type-examination
negotiated with the other certification,
(c)) the technical documentation that will allow the assessment of conformity and assessment
the suitability of the safety component, so that the lift to which it is
correctly fitted to conform with the provisions of this regulation. For the purpose of assessing the
conformity is necessary to make the technical documentation included
1. General description of the safety component, including the intended area of use
(in particular any speed limit, load and power) and conditions
(in particular, atmospheres, effects of climate conditions),
2. Design and manufacturing drawings or diagrams,
3. the basic requirement (requirements) and the measures adopted for its
(their) meet (for example, by reference to the use of harmonised the Czech
technical standards),
4. the results of any tests or calculations carried out by the manufacturer of the safety
or specified components (in this case, information about the person who
tests or calculations carried out),
5. instructions for installation of the safety components,
6. Description of the measures carried out at the production stage to ensure that series-
manufactured safety components were identical to the tested sample
the safety components,
d) sample of the safety component or the exact location where can
be tested. Notified body may request further samples.
3. the notified provides
1. the assessment of the technical documentation that meets the intended purpose,
2. type-examination of safety components to verify that corresponds to the
the technical documentation,
3. the necessary examinations and tests to be carried out, or have carried out, in order to
check whether the solutions adopted by the manufacturer of the safety component meet the
requirements and allow to fulfil its function of the safety component,
If it is correctly fitted on a lift.
4. If the sample of the safety component meet the essential requirements,
notified shall issue the EC type-examination certificate (hereinafter referred to as
"the type-examination certificate"). The certificate contains the identification data
about the manufacturer of the safety component, conclusions of the examination, the conditions of
the validity of the certificate and the data needed for identification of the certified
the type of safety components.
If the notified person refuses the manufacturer of the safety component
issue a type-examination certificate must include detailed reasons for
This refusal. At the same time must be given for the opposition procedure.
5. the manufacturer of the safety component or his authorized representative
inform the person of any change to the certification, which was carried out
or plans to make to certified safety component,
including changes or adjustments that were not specified in the original technical
the documentation. Notified will assess the changes and notify the applicant about the
whether the original type-examination certificate shall also apply for the safety
the component with the changes or whether it is necessary to perform a new
the type of certification, where appropriate, the original type certificate. ^ 5)
6. each notified body shall notify the Member States of the European
the Union of the necessary information, concerning
and the type-examination certificates issued);
(b)) taken from type-examination certificates.
Each notified body must also give the note to the other
the competent notified persons necessary information relating to the
type-examination certificates withdrawn.
7. the type-examination certificate, the documentation and correspondence related
to the course of type-examination shall be drawn up in the Czech language and
also, where applicable, in the language, which notified the manufacturer agrees with
the safety components or his authorized representative.
8. the manufacturer of the safety component or his authorized representative must
keep a copy of the type-examination certificate and its additions, together
with the technical documentation for a period of 10 years from the time when it was made
the last safety component.
If the manufacturer of the safety components or his authorized representative
registered office in the community, shall be responsible for keeping the necessary
the technical documentation shall specify the person that the safety component on the
the Community market.
(B).
TYPE-EXAMINATION OF LIFTS
1. Type-examination is the procedure whereby a notified body ascertains and
certifies that a model lift, or such a lift, for which have been made
any changes or modifications, complies with the requirements of this regulation of the Government.
2. the installer of the lift provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the details of the place of manufacture of the lift,
(b)) a written declaration that the Treaty was not to carry out type-examination
agreed with another person, by
(c)) the technical documentation that will allow assessment of the conformity of the lift with the
the provisions of this regulation and to the understanding of the construction and operation of the lift.
In this context, it is necessary that for the purposes of assessing the conformity of the technical
the documentation contained
1. General description of the representative type of the lift; technical documentation has
clearly establish all the permissible adjustments
2. Design and manufacturing drawings or diagrams,
3. basic requirements and considered the measures taken to meet them
(e.g. reference to harmonised the Czech technical standard),
4. a copy of the Declaration of conformity of the safety components used in the
the manufacture of the lift,
5. the results of any tests or calculations carried out or supplied
the supplier of the lift,
6. specimen of the instructions for use of the lift,
7. measures carried out during the Assembly to ensure that the series-
produced by the elevators, complied with the provisions of this regulation.
(d)) of the place where the information can be typed representative of the elevator.
The lift is the type representative checked in the final implementation, and must
to be able to operate at least three stations (top, middle and bottom).
3. the notified provides
and the assessment of technical documentation) that performs the desired aims,
(b) the type-examination of a representative of the lift) to verify whether it was produced
in accordance with the technical documentation,
(c)), the necessary checks and tests to be carried out, or have carried out for
Verify whether the solutions adopted by the installer of a lift with the essential
requirements and allow them to be matched.
4. If the type representative lift provisions of this regulation,
that are applicable to it, has notified the EC certificate
type examination (hereinafter referred to as "the type-examination certificate"). Certificate
contains identifying information about the suppliers of the lift, the conclusions of the examinations,
the conditions of validity of the certificate and the data necessary to identify the
certified elevator type.
The Commission, the Member States of the European Union and other relevant notified
persons may receive a copy of the type-examination certificate and to the
the basis of a reasoned request, a copy of the technical documentation,
carried out the tests, calculations and tests.
If the notified body refuses to issue a lift
type-examination certificate must include detailed reasons for this
the refusal. At the same time must be given for the opposition procedure.
5. The lift must inform the person of any change to the certification
or edit that was made or plans to make to the
a certified type of lift, including new extensions or variants not
specified in the original technical dossier. Notified body shall assess the
the changes and inform the applicant whether the type-examination certificate shall also apply
for the elevator with the changes or whether it is necessary to perform a new
the type of certification, where appropriate, the original type-examination certificate
make up. ^ 6)
6. each notified body shall notify the Member States of the European
the Union of the necessary information, concerning
and the type-examination certificates issued);
(b)) taken from type-examination certificates.
Each notified body must also give the note to the other
the competent notified persons information regarding the collected
type-examination certificates.
7. the type-examination certificate, the documentation and correspondence, related
to the course of type-examination shall be drawn up in the Czech language and
also, where applicable, in the language, which notified the supplier shall agree with the
the elevator.
8. the installer of the lift must keep with the technical documentation copies of the
type-examination certificates and their additions for a period of 10 years from the time
When it was made the same as the last elevator lift.
Annex 6
FINAL INSPECTION
1. Final inspection is the procedure whereby the installer of a lift that meets the
the provisions of point 2, and declares that the lift which shows the
market, complies with the essential requirements. The lift is placing the CE marking
in the cage each elevator and issued a declaration of conformity.
2. the installer of the lift shall carry out any measures to lift, which lists the
the market coincided with the certified elevator type as described in the certificate
type-examination and meet the basic requirements, which
apply.
3. the installer of the lift shall keep for 10 years from the date when the lift is placed on the
the market, a copy of the Declaration of conformity and the final inspection certificate,
referred to in point 6.
4. the notified body chosen by the supplier of the lift carries out or causes
perform on the elevator, which is to be placed on the market, the appropriate tests and
control, defined in the respective Czech technical standards (section 2)
or equivalent tests, which shall verify compliance with the essential requirements.
These checks and tests shall cover in particular
and an assessment of the findings of the documentation) that the lift conforms with the type
representative of the elevator, which was released in the type-examination certificate
accordance with part B of annex 5 to this regulation,
(b)) functional testing of empty and loaded up the elevator to
Verify the correct installation and function of the safety devices (end
switches, locking devices and the like),
-functional test of the elevator at maximum load and no load for
Verify the correct operation of the safety devices in the event of a power failure
the stream;
-static test with a load equal to 1.25 times nominal
the load, which corresponds to point 5.1 of annex 1 to this regulation.
After performing these tests verify that the notified person not to
no distortion or damage that could endanger the use of the elevator.
5. Lift passes notified the person of the following documentation:
and the drawing of the complete lift report),
(b)) the drawings and diagrams necessary for final inspection, in particular schemes
the control circuit
(c) instructions for use of the lift) according to point 6.2 of annex 1 to this
of the regulation.
Notified may not require detailed plans or detailed
information that is not necessary for verifying the conformity of the lift, and which shall be
placed on the market, with the type as described in the certificate of elevator representative
type-examination.
6. If the lift satisfies the provisions of this regulation, notified
a person joins or leaves the vendor connect to CE mark its
the identification number in accordance with section 4 and shall issue a certificate of final
inspection, indicating the tests carried out and checks.
Notified person fills in the relevant information in the logbook referred to in point 6.2.
Annex 1 to this regulation.
If the notified body refuses to issue a certificate of final
inspection must include detailed reasons for the refusal and to propose a way to
How to achieve approval. If the lift again applies for
final inspection, must apply for the same notified persons.
7. The final inspection certificate, dossiers and
correspondence relating to the conformity assessment shall be drawn up in
the Czech language and, where appropriate, also in a language that the person notified
agree with the supplier of the elevator.
Annex 7
THE CONDITIONS FOR THE AUTHORIZATION OF
1. The Director of the authorized persons and its staff responsible for
inspections and tests shall not be the designer, designer,
the supplier or manufacturer of safety components or the supplier of the lifts,
which carries out inspection, nor the authorised representative of any of the
These parties. The Director of the authorized persons and its staff
responsible for the assessment procedures of quality assurance systems for the assessment of
conformity in accordance with section 3 shall not be the designer, designer, contractor or
the manufacturer of the safety components or the supplier of the lifts, for which
carries out inspection, nor the authorised representative of any of these parties.
The Director of the authorized persons and its employees shall not be
involved directly or as authorized representatives in the design, manufacture,
marketing service or safety components or on delivery of the lift.
This does not preclude the possibility of exchanges of technical information in the middle of the manufacturer
of the safety components or the supplier of the lift and the authorized
person.
2. the Authorized person and its personnel must carry out the inspection
and tests with the highest degree of professional integrity and technical
eligibility and shall not operate any pressures and inducements, in particular
financial, which might influence their judgement or the results of the
the inspection, especially from persons or groups of persons that are interested in
on the scan results.
3. the Authorised person shall have the necessary staff and
possess the necessary facilities to enable it to perform properly the administrative
and technical tasks connected with the inspection and tests; must also have access
to the equipment required for special verification.
4. The staff responsible for inspection must have
and) good technical and professional training;
(b) satisfactory knowledge of the requirements) of the trials and the corresponding
experience with these tests;
(c) the ability to draw up certificates), records and reports required to
proof testing.
5. Must be guaranteed the impartiality of the employees carrying out the inspection.
The remuneration of employees shall not depend on the number of tests carried out or on the
the results of these tests.
6. the Authorised person shall conclude a liability insurance.
7. Confidentiality of employees (section 20a of Act).
Annex 8
QUALITY ASSURANCE OF SAFETY COMPONENTS
(Conformity assessment procedure (E))
1. the safety components of the quality assurance is the procedure whereby the
the manufacturer of the safety component for fulfilling the point 2 and convinces
hereby declares that the safety components are identical with the type as described in the
type-examination certificate and satisfy the requirements of this regulation, which
apply to them, and that a properly fitted safety component
allow the lift to meet basic requirements.
The manufacturer of the safety component or his authorized representative shall be placed
for each matching safety component of the CE marking and shall
the Declaration of conformity. The CE marking shall complete the identification number
obtain from the person responsible for the surveillance as specified in point 4.
2. the manufacturer of the safety component applies the system of quality assurance
quality for the final inspection of the safety components and testing
referred to in point 3 and is subject to surveillance as specified in point 4.
3. Quality assurance system
3.1. The manufacturer of the safety component must lodge an application for assessment of his
the quality assurance system for safety components in
notified the person of their choice.
The manufacturer of the safety components or his authorized representative
provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the details of the place of manufacture of the safety component,
(b)) all relevant information on safety components,
(c)) the quality assurance system documentation,
(d)) the technical documentation relating to the safety components and a copy of the
type-examination certificates.
3.2. Under the quality assurance system must be any security
component testing and the test must be carried out as laid down in
the respective Czech technical standards referred to in section 2 (2). 8 or
equivalent tests, in order to be verified by compliance with the essential requirements.
All system elements, requirements and provisions adopted by the manufacturer
the safety components must be systematically and properly in writing
documented in the form of instructions, procedures and instructions. This documentation
the quality assurance system must permit a uniform interpretation of
programmes, plans, manuals and quality records.
The documentation includes in particular an adequate description of the
and) the quality objectives,
(b)) the organizational structure, responsibilities and powers of the management in relation to the
the quality of the safety components,
(c)) tests that will be carried out after manufacture,
(d) funding for the verification of effective) functioning of the system
the quality,
e) quality records, such as inspection reports, test results,
data, calibration data, qualification reports of the personnel concerned and so
further.
3.3 the notified body assesses the quality assurance system, to
determine whether it satisfies the requirements referred to in point 3.2. Presumption of conformity with the
These requirements on quality assurance systems is fulfilled for systems
the quality that correspond to the respective Czech technical harmonised
standard. ' ^ 7)
In the Group conducting the assessment must be at least one Member
experience in elevator technology assessment. Assessment procedure must
include a visit to the manufacturer of the safety components.
The results of the assessment are reported in writing by the manufacturer of the safety
components. The communication must contain the conclusions of the examination and the justification
its decision on the assessment.
3.4. the manufacturer of the safety components ensures fulfilment of obligations
arising out of the quality assurance system posouzeného and keeps it
so that was still reasonable and effective.
The manufacturer of the safety components or his authorized representative
shall be kept informed by the person who assessed the system
quality assurance of any intended change of the system.
Notified body shall evaluate the proposed modifications and decide whether the amended
the quality assurance system will still satisfy the requirements of
referred to in point 3.2 or whether to carry out a new assessment.
The result of assessment shall inform the manufacturer or his authorised representative.
The communication contains the conclusions of the assessment, including the justification of its decision to
the assessment.
4. supervision by the person
4.1. The purpose of surveillance is to ensure that the manufacturer of the safety component
duly fulfils the obligations arising out of the quality assurance system.
4.2 for the purposes of supervision, the manufacturer of the safety components allows you to
the notified person entrance into the sampling, testing and storage
space and provide the necessary supporting documents, in particular,
and the quality assurance system documentation),
(b)) the technical documentation,
(c)) the quality records, such as reports on the inspections and test results,
data, calibration data, qualification reports of the personnel concerned.
4.3 the notified body carries out periodic monitoring, to be assured that the
the manufacturer of the safety components maintains and applies the quality assurance system
quality and provide the manufacturer of the safety component on the results
supervision.
4.4 in addition, the notified body may carry out the manufacturer of the safety
unannounced surveillance components.
When an unsolicited supervision can notified, if necessary,
perform or specify tests to verify the correct function
the quality assurance system. The manufacturer of the safety components passes
notified on the results of the surveillance, and in the case of the implementation of
test and report on the results of the test.
Report on the results of the surveillance, where appropriate, tests shall draw up in the Czech language
and, where appropriate, also in a language that the person notified by the manufacturer agrees with
the safety components.
5. the manufacturer of the safety components or his authorized representative
must over a period of ten years from the last date of manufacture of the safety component,
keep available for the national authorities:
and) the documentation referred to in point 3.1. (d),
(b)), the updating referred to in second paragraph of 3.4;
(c)) decision and notified the persons referred to in the last paragraph of
section 3.4, and in 4.3 and 4.4.
6. each notified body must give the other competent
sighted people relevant information on issued and revoked
approvals of quality assurance systems.
Annex 9
COMPREHENSIVE QUALITY ASSURANCE OF SAFETY COMPONENTS
(Conformity assessment procedure (H))
1. Full quality assurance is the procedure of safety components
by the manufacturer of the safety component fulfils the obligations referred to in
point 2 is convincing and declares that the safety components satisfy the
the basic requirements and that the safety component will enable a lift to
which it is correctly fitted to satisfy the essential requirements. The manufacturer of the
of the safety component or his authorized representative shall be placed on
each complying with the safety component of the CE marking and issue a statement
of conformity. The CE marking shall complete the identification number of the notified persons
responsible for the surveillance as specified in point 4.
2. the manufacturer of the safety component applies the quality assurance system
quality for the design, manufacture and final inspection of the safety
components and testing as specified in point 3 and is subject to surveillance as specified in point 4.
3. Quality assurance system
3.1. The manufacturer of the safety component must lodge an application for assessment of his
the quality assurance system by the notified person of their choice.
The manufacturer of the safety components or his authorized representative
provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the details of the place of manufacture of the safety component;
(b)) all relevant information on safety components;
(c) the quality assurance system documentation).
3.2. the quality system must ensure that the safety
the components meet the essential requirements and to enable to lift
which they are mounted, these basic requirements.
All system elements, requirements and provisions adopted by the manufacturer
the safety components must be systematically and properly in writing
documented in the form of instructions, procedures and instructions. This documentation
the quality assurance system must permit a uniform interpretation of
programmes, plans, manuals and quality records.
The documentation includes in particular an adequate description of the
and) the quality objectives and the organisational structure, responsibilities and powers of the
leadership in relation to the design and quality of the safety components,
(b)) the technical design specifications including used Czech technical
standards, and if they are not fully used the Czech technical standards referred to in section 2 of the
paragraph. 8, the resources used for security and meet the essential
requirements that apply to the safety components,
(c)) and checks the authentication methods of the structure, processes and systematic
the activities, which will be used when designing security
components,
(d) the respective production processes used), quality control, and
quality assurance and systematic activities,
(e)) carried out the examination and tests used in pre-production,
production and post-production phase and periodicity with which they are carried out,
(f)) quality records, such as reports on the monitoring and test results,
calibration data, records of the qualifications of the personnel concerned and so
further,
(g)) the means by which you can monitor whether they have achieved the required quality
the design and the product and the effective functioning of the quality assurance system
the quality.
3.3 the notified body assesses the quality assurance system, to
determine whether it satisfies the requirements referred to in point 3.2. Presumption of conformity with the
These requirements on quality assurance systems is fulfilled for systems
the quality that correspond to the respective Czech technical standard. ' ^ 8)
In the Group conducting the assessment must be at least one Member
experience in elevator technology assessment. Assessment procedure must
include a visit to the manufacturer of the safety components.
The results of the assessment are reported in writing by the manufacturer of the safety
components. The communication must contain the conclusions of the examination and the justification
its decision on the assessment.
3.4. the manufacturer of the safety components ensures fulfilment of obligations
arising out of the quality assurance system posouzeného and keeps it
so that was still reasonable and effective.
The manufacturer of the safety components or his authorized representative
shall be kept informed by the person who assessed the system
quality assurance of any intended change of the system.
Notified body shall assess the proposed changes and decide whether the amended
the quality assurance system will still satisfy the requirements referred to in
section 3.2, or whether to carry out a new assessment.
The result of assessment shall inform the manufacturer or his authorised representative.
The communication contains the conclusions of the assessment, including the justification of its decision to
the assessment.
4. supervision by the person
4.1. The purpose of surveillance is to ensure that the manufacturer of the safety components
properly fulfils its obligations arising from the quality assurance system
the quality.
4.2 for the purposes of supervision, the manufacturer of the safety components allows you to
notified the person access to the design, production, inspection,
testing and storage premises and provide the necessary supporting documents,
in particular, the
and the quality assurance system documentation),
(b)) the quality records provided by the project of the system
quality assurance, e.g.. the results of analyses, calculations, tests, and so
further,
(c)) the quality records, provided in the production part of the system
quality assurance, e.g.. inspection reports, test data,
calibration data, qualification reports of the staff, and so on.
4.3 the notified body carries out periodic monitoring, to be assured that the
the manufacturer of the safety components maintains and applies the quality assurance system
quality, and provide the manufacturer of the safety components on the results
supervision.
4.4 in addition, the notified body may carry out the manufacturer of the safety
unannounced surveillance components.
When an unsolicited supervision can notified, if necessary,
perform or specify tests to verify the correct function
the quality assurance system. The manufacturer of the safety components passes
notified on the results of the surveillance, and in the case of the implementation of
test and report on the results of the test.
5. the manufacturer of the safety components or his authorized representative
After a period of ten years from the date of manufacture of the last security
store the components available to the national authorities
and) the documentation referred to in point 3.1. (b),
(b)), the updating referred to in second paragraph of 3.4;
(c)) decision and notified the persons referred to in the last paragraph of
section 3.4, and in 4.3 and 4.4.
If the manufacturer of the safety components or his authorized representative
registered office in the community, the obligation to keep available the technical
documentation on the person responsible for placing the safety components on
the Community market.
6. each notified body must give the other competent
sighted people relevant information on issued and revoked
approvals of quality assurance systems.
7. Documentation and correspondence relating to the procedures of the comprehensive
quality assurance shall be drawn up in the Czech language and, where appropriate,
also in a language that the person notified by the manufacturer agrees with security
component or his authorized representative.
Annex 10
VERIFICATION OF THE CONFORMITY OF EACH ELEVATOR
(Conformity assessment procedure (G))
1. Verification of compliance of each elevator certification is the procedure by which
the installer of the lift and convinces declares that the lift which is being placed
on the market and has received the certificate of conformity referred to in section 4., meets the requirements of
This regulation, which is applicable to it. The lift places
CE marking in the cage elevator, and issued a declaration of conformity.
2. the installer of the lift shall request verification of conformity of individual elevators for
notified the person of their choice.
A lift provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the data on the place of production of the lift;
(b)) a written declaration that the same application has not been lodged with any other
notified of the person;
(c)) the technical documentation.
3. the aim of the technical documentation is to enable conformity assessment of the lift
the requirements of this regulation and the understanding of the design, installation and operation
the elevator.
If it is necessary for the assessment of conformity, the technical documentation
contains
and a general description of the lift,)
(b) the) drawings and diagrams relating to the design and production,
(c)), the relevant essential requirements and the solutions adopted for the purpose of their
meet (for example, a reference to the use of harmonised the Czech technical
the standards),
d) test results or calculations carried out or supplied by the supplier
the elevator,
(e) the instructions for use of the lift),
(f) a copy of the type-examination certificates) used the safety
components.
4. the notified body shall examine the technical documentation, and carry out
appropriate tests of the lift prescribed in the relevant Czech technical
standards referred to in section 2 of this regulation, or equivalent tests, in order to
found its conformity with the requirements of this regulation.
If the lift satisfies the provisions of this regulation, notified
joins or leaves to join their identification number in accordance with § 4 and
According to tests carried out shall issue a certificate of conformity.
Notified relevant parties will fill in the book of the lift in accordance with section 6.2 of the
Annex 1 to this regulation.
If the notified body refuses to issue a certificate of conformity, it shall indicate in a
the report detailed the reasons for the refusal and will propose a way to achieve
axle. New verification of conformity with the type certified ensures vendor
the elevator in the same notified persons.
5. The certificate of conformity and the dossiers and correspondence relating to the processes of
authentication of individual products must be drawn up in the Czech language and
also, where applicable, in the language, which notified the supplier shall agree with the
the elevator.
6. the installer of the lift shall keep the technical documentation and a copy of the certificate
of conformity for a period of 10 years from the time when the lift is placed on the market.
Annex 11
ASSESSMENT OF THE CONFORMITY OF THE SAFETY COMPONENTS WITH THE TYPE ●
(Conformity assessment procedure (C))
1. assessment of the conformity of the safety components with the type ●
random control is the procedure whereby the manufacturer of the safety
components or his authorized representative convinces and declares that the
safety components are identical with the type as described in the certificate
type-examination and satisfy the requirements of this regulation, the
cover, and allow any lift to which they are correctly
fitted to satisfy the essential requirements of this regulation.
The manufacturer of the safety components or his authorized representative
affix the CE marking to each safety component and draw up a declaration
of conformity. The manufacturer of the safety components or his authorized
shortcut indicates the safety component identification number
notified persons already during the manufacturing process.
2. the manufacturer of the safety components ensures all necessary measures
to ensure that the manufacturing process ensures compliance of the manufactured safety
components with the type as described in the type-examination certificate and with the requirements of
This regulation, which will apply to them.
3. the manufacturer of the safety components or his authorized representative
must keep a copy of the Declaration of conformity for a period of ten years from the date of
the last production of the safety components.
If the manufacturer of the safety components or his authorized representative
registered office in the community, the obligation to keep available the technical
documentation of the person responsible for placing on the market of the safety component,
The community.
4. the notified body chosen by the manufacturer of the safety components, the person performs
or have it perform in random intervals a sample check
the safety components. Examines a sample made
the safety components on the spot taken by the person and the
performs to verify the conformity of the product with the relevant requirements of this
Regulation of the appropriate tests defined in the relevant Czech
the technical standards according to § 2 (2). 8 or equivalent tests.
If one or more of the controlled safety components
are not identical to the certified type, passes about notified
the report of the manufacturer of the safety component or the authorised representative,
to avoid putting these safety components on the market.
The aspects that must be taken into account in the monitoring of safety
components, will be determined by mutual agreement of all the notified persons
dealing with this procedure, taking into account the basic
the parameters of the safety components listed in annex 4 to this
of the regulation.
5. The dossiers and correspondence relating to the random checks pursuant to
point 4 shall be drawn up in the Czech language and also, where applicable, in the language of that
notified body shall agree with the manufacturer of the safety components or the
his authorised representative.
Annex 12
PRODUCT QUALITY ASSURANCE
(Conformity assessment procedure (E))
1. Product quality assurance is the procedure whereby the installer of a lift
complying with the provisions of point 2 convinces and declares that mounted
the elevators are in conformity with the type as described in the type-examination certificate and
meet the requirements of this regulation which apply to it.
The lift shall affix to each matching elevator of the CE marking and shall
the Declaration of conformity. The CE marking must be accompanied by the identification number of the
notified persons conducting surveillance as specified in point 4.
2. The lift installer applies the quality assurance system for
final inspection and testing of lifts according to point 3, and is subject to
surveillance as specified in point 4.
3. Quality assurance system
3.1. the installer of a lift must lodge an application for assessment of your system
quality assurance for lifts for persons notified in accordance with its
the selection.
A lift provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the details of the place of manufacture of the lift,
(b)) all necessary information for the lifts,
(c)) the quality assurance system documentation,
(d)) and a copy of the technical documentation of the lifts, type-examination certificates.
3.2. Under the quality assurance system, each lift must be
examined, and that was verified its conformity with the requirements of this regulation,
which apply to it, appropriate tests shall be carried out as laid down in
the respective Czech technical standards according to § 2 (2). 8 or the test
equivalent.
All system elements, requirements and provisions adopted by the installer of a lift
must be systematically and properly documented in writing in the form of instructions,
procedures and instructions. This quality assurance system documentation must
allow the Simp
otnou interpretation programmes, plans, manuals and quality records.
The documentation includes in particular an adequate description of the
and) the quality objectives,
(b)) the organizational structure, responsibilities and powers of the management in relation to the
the quality of the lifts,
(c)) and checking tests that will be carried out before placing on the market,
containing mainly the tests referred to in annex 6 to this regulation,
(d) the means of verifying the effective functioning of the) assurance system
the quality,
e) quality records, such as. the inspection report and test results,
data, calibration data, qualification reports of the personnel concerned and so
further.
3.3 the notified body assesses the quality assurance system, to
determine whether it satisfies the requirements referred to in point 3.2. Presumption of conformity with the
These requirements on quality assurance systems is fulfilled for systems
the quality that correspond to the respective Czech technical standard. ' ^ 9)
In the Group conducting the assessment must be at least one Member
experience in elevator technology assessment. The assessment procedure includes
surveillance in the workplace of the lift and the installation of a lift.
The results of the assessment are communicated to the supplier in writing. Notification
contains the conclusions of the examination and the assessment's conclusion justified.
3.4. the installer of the lift shall ensure the execution of the obligations arising from the
posouzeného quality assurance system and maintain it so that it was
remains adequate and efficient.
The lift shall be kept informed by the person that
assess the quality assurance system informed of any intended change
the quality assurance system.
Notified body shall assess the proposed changes and decide whether the amended
the quality assurance system will still satisfy the requirements of
referred to in point 3.2 or whether a reassessment is required to perform.
The decision to announce the lift. The notification shall contain the conclusions of the
checking and justified the conclusion of the assessment.
4. supervision by the person
4.1. The purpose of surveillance is to ensure that the installer of a lift duly fulfils the
the obligations arising from the quality assurance system.
4.2 For the purposes of supervision of the lift allows you to obtain from the person
entry to the control and test area and provides the necessary
supporting documents, in particular the
and the quality assurance system documentation),
(b)) the technical documentation,
(c)) the quality records, such as. reports on inspections and test results,
data, calibration data, qualification reports of the personnel concerned and so
further.
4.3 the notified body carries out periodic monitoring, to be assured that the
of a lift maintains and applies the quality assurance system and
lift passes, a report on the results of supervision.
4.4 in addition, the notified body may make unannounced supervision on the spot
the installation of the elevator.
When an unsolicited supervision can notified, if necessary,
perform or specify tests to verify the correct function
the quality assurance system. Notified to the supplier provides
the elevator on the results of supervision, and in the case of a test and
report on the results of the tests.
5. the installer of a lift must, for a period of ten years from the date of production of the last
an elevator, keep available for the national authorities:
and) the documentation referred to in point 3.1. (c)),
(b)) changes referred to in the second paragraph of point 3.4;
(c)) decision and notified the persons referred to in the last paragraph of
section 3.4, and in 4.3 and 4.4.
6. each notified body provides other relevant notified
persons with the relevant information on issued and revoked approvals systems
quality assurance.
7. Documentation and correspondence relating to the process of securing
the quality of the lifts shall be drawn up in the Czech language and, where appropriate, in
language, which notified the supplier shall agree with the elevator.
Annex 13
COMPREHENSIVE QUALITY ASSURANCE FOR LIFTS
(Conformity assessment procedure (H))
1. Full quality assurance is the procedure whereby a supplier
an elevator complying with the provisions of section 2, persuades and declares that the
lifts comply with the essential requirements of this regulation, the
apply.
The lift connects the CE marking to each lift and draw up a
the Declaration of conformity. The CE marking must be accompanied by the identification number of the
notified persons conducting surveillance as specified in point 4.
2. The lift installer applies the quality assurance system for
design, manufacture, Assembly, mounting internal and external final
inspection of the lift in accordance with point 3, and is subject to surveillance as specified in point 4.
3. Quality assurance system
3.1. the installer of a lift must lodge an application for assessment of his quality system for the
the elevators at the notified person of their choice.
A lift provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the data on the place of production of the lift.
(b)) all relevant information on the lifts, in particular information which
contribute to the understanding of the relationship between the construction and operation of the lift and allows
the assessment of conformity with the requirements of this regulation;
(c) the quality assurance system documentation).
3.2. The quality assurance system must ensure compliance of the lifts with the
the essential requirements of this regulation which apply to them.
All system elements, requirements and provisions adopted by the installer of a lift
must be systematically and properly documented in writing in the form of instructions,
procedures and instructions. This quality assurance system documentation must
allow uniform interpretation programmes, plans, manuals and records
the quality.
The documentation includes in particular an adequate description of the
and) the quality objectives and the organisational structure, responsibilities and powers of the
leadership in relation to the design and quality of the lifts,
(b) the technical construction specifications including) used the Czech
technical standards and, if not fully used the Czech technical standards
listed in section 2 of this regulation, the funds used for security
compliance with the essential requirements of this regulation relating to lifts
(c)) and checks the authentication methods of the structure, processes and systematic
the activities, which will be used when designing the lifts,
(d)) tests that will be carried out in the přejímkách of materials, components and
sub-assemblies,
(e)) of the corresponding methods in the production installation, Assembly, quality control,
processes and systematic actions that will be used,
f) tests that will be carried out before (inspection of installation
conditions: shaft, housing of machinery and so on), during and after installation
(including in particular the tests given in annex 6 to this Regulation),
(g)) the quality records, such as reports and test results, information on the
calibration, qualification reports of the personnel concerned and so on,
h) means that you can watch, whether you have reached the required quality
construction and Assembly, and the effective functioning of the quality assurance system
the quality.
3.3 assessment of design documentation
If the design documentation is not entirely in accordance with harmonized
Czech technical standards, notified to determine whether
design documentation corresponds to the provisions of this regulation and, if
This is the case, shall issue a certificate of assessment of the lift EC design
the documentation shall indicate the conditions of validity of the certificate and details for
identify this assessed the design documentation.
3.4 assessment of the quality assurance system
Notified body assesses the quality assurance system to determine
whether it satisfies the requirements referred to in point 3.2. Presumption of conformity with the following
the requirements for quality assurance systems is met by the quality system,
that correspond to the respective Czech technical standard. ' ^ 10)
In the Group conducting the assessment must be at least one Member
experience in elevator technology assessment. The assessment procedure includes
surveillance in the workplace and on-the-spot Assembly supplier of the lift.
The results of the assessment are communicated to the supplier in writing. Notification
It contains the findings of the tests and justified the conclusion of the assessment.
3.5 lift ensures fulfilment of obligations arising from the
posouzeného quality assurance system, and maintain it so that it was
remains adequate and efficient.
The lift shall be kept informed by the person who
assess the quality assurance system informed of any intended change
the quality assurance system.
Notified person shall examine the proposed changes and decide whether the amended
the quality assurance system will still satisfy the requirements of
referred to in point 3.2 or whether a reassessment is required.
The results of the assessment indicates the lift installer. The notice contains
the conclusions of the assessment, including the justification of its decision on the assessment.
4. supervision by the person
4.1. The purpose of surveillance is to ensure that the installer of a lift duly fulfils the
the obligations arising from the quality assurance system.
4.2 For the purposes of supervision of the lift allows you to obtain from the person
input into the design, production, Assembly, inspection, test
and storage space and provide the necessary supporting documents, in particular the
and the quality assurance system documentation);
(b)) quality records relating to the components of the system
quality assurance, such as results of analyses, calculations, tests, and
so on;
(c) quality records) in the part of the quality system relating to
the final deliveries, installation, for example, reports on the inspections and the results
and test data, calibration data, qualification reports of the personnel concerned,
and so on.
4.3 the notified body carries out periodic monitoring, to be assured that the
of a lift maintains and applies the quality assurance system, and
lift passes on the results of supervision.
4.4 in addition, the notified body may make unannounced surveillance
the workplace of the lift and the installation of a lift. When
an unsolicited supervision may be notified, if necessary,
perform or specify tests to verify the correct function
the quality assurance system. About an unsolicited monitoring relays
notified person lift and test
and report on the results of the tests.
5. the installer of a lift must, for a period of ten years from the placing on the market
keep available for the national authorities
and) the documentation referred to in point 3.1. (c),
(b)), the updating referred to in second paragraph of point 3.5;
(c)) decision and notified the persons referred to in the last paragraph of
section 3.5 and in sections 4.3 and 4.4.
If the supplier does not have a lift seat in the European Union, the obligation to
by the person.
6. each notified body shall give the other competent person notified
persons with the relevant information on issued and revoked certificates
quality assurance systems.
7. Documentation and correspondence relating to the procedures of the comprehensive
quality assurance shall be drawn up in the Czech language and, where appropriate,
also in a language that the person notified by the supplier shall agree with the elevator.
Annex 14
PRODUCTION QUALITY ASSURANCE FOR LIFTS
(Conformity assessment procedure (D))
1. Production quality assurance is the procedure whereby the installer of a lift
complying with the provisions of section 2, persuades and declares that the lifts
comply with the requirements of this regulation, the Governments that apply to them.
The lift connects the CE marking on each lift and draw up a written
the Declaration of conformity. The CE marking must be accompanied by the identification number of the
notified of the person who is responsible for the surveillance as specified in point 4.
2. the installer of the lift system for quality assurance in production,
installation, final inspection and testing as specified in point 3 and must be subject to
surveillance as specified in point 4.
3. Quality assurance system
3.1. the installer of a lift must lodge an application for assessment of your system
quality assurance for notified the person of their choice.
A lift provides the notified person
and your identifying information) (for a natural person name and surname and the Permanent
residence or place of business, in the case of a legal person the name or business name
and its headquarters) and the data on the place of production of the lift.
(b)) all relevant information on the lifts,
(c)) the quality assurance system documentation,
(d) the technical documentation of the approved type) and a copy of the certificate
type-examination.
3.2. the quality system must ensure that the lifts satisfy
the requirements of this regulation which apply to them.
All system elements, requirements and provisions adopted by the installer of a lift
must be systematically and properly documented in writing in the form of instructions,
procedures and instructions. This quality assurance system documentation must
allow uniform interpretation programmes, plans, manuals and records
the quality.
The documentation includes in particular an adequate description of the
and) the quality objectives and the organisational structure, responsibilities and powers of the
leadership in relation to the quality of the lifts,
(b)), production processes, quality assurance and inspection methods, procedures and
systematic actions that will be used,
(c)) the examination and tests carried out before, during and after
Assembly, which shall include at least the tests in accordance with point 4 (b) of annex 6 to the
of this regulation,
d) quality records, such as inspection reports and test results,
data, calibration data, qualification reports of the personnel concerned and so
further,
(e)) the means by which you can monitor whether they have achieved the required quality
the elevator and the effective operation of the quality system.
3.3 the notified body assesses the quality assurance system, to
determine whether it satisfies the requirements referred to in point 3.2. Presumption of conformity with the
These quality systems requirements is fulfilled with quality systems, which
correspond to the respective Czech technical standard. ' ^ 11)
In the Group conducting the assessment must be at least one Member
experience in elevator technology assessment. The assessment procedure includes
surveillance in the workplace of the lift.
The results of the assessment are communicated to the supplier in writing. Notification
It contains the findings of the tests and justified the conclusion of the assessment.
3.4. the installer of the lift shall ensure the execution of the obligations arising from the system
quality assurance, and maintains it was still reasonable and
effective.
The lift shall be kept informed by the person who
assess the quality assurance system informed of any intended change
the quality assurance system.
Notified person shall examine the proposed changes and decide whether the amended
the quality assurance system will still satisfy the requirements of
referred to in point 3.2 or whether a reassessment is to be made.
The result of the assessment indicates the lift installer. The notification must contain
the conclusions of the assessment, including the preamble.
4. supervision by the person
4.1. The purpose of surveillance is to ensure that the installer of a lift duly fulfils the
the obligations arising from the quality assurance system.
4.2 For the purposes of supervision of the lift allows you to obtain from the person
access to production, Assembly, inspection, testing and storage
space, and provide all necessary information, in particular
and the quality assurance system documentation),
(b)) the quality records, such as inspection reports and test results,
data, calibration data, qualification reports of the personnel concerned and so
further.
4.3 the notified body carries out regular oversight to be assured that the
of a lift maintains and applies the quality assurance system, and
lift passes on the results of supervision.
4.4 in addition, the notified body may make unannounced monitoring in
the lift. This surveillance may an unsolicited notified
person, if necessary, carry out or provide for the conduct of tests
verification of the correct operation of the quality assurance system. For an unsolicited
the surveillance passes notified lift and
test, and report on the results of the tests.
5. the installer of a lift must, for a period of at least ten years from the date of manufacture
the last lift to keep available for the national authorities.
and) the documentation referred to in point 3.1,
(b)), the updating referred to in second paragraph of point 3.4,
(c)) decision and notified the persons referred to in the last paragraph of
section 3.4, and in 4.3 and 4.4.
6. each notified body must give the other competent
sighted people relevant information on issued and revoked
approvals of quality assurance systems.
7. Documentation and correspondence relating to the assurance procedures
the quality of the production shall be drawn up in the Czech language and, where appropriate, also in the language,
who notified the supplier shall agree with the elevator.
1) European Parliament and Council Directive 95/16/EC of 29. June 1995 on the
approximation of the laws of the Member States relating to lifts.
2 § 2 (b)). I) of Act No. 22/1997 Coll., as amended by Act No. 204/2002 Sb.
3) Government Regulation No. 291/2000 Coll., laying down the graphic form of the
the CE marking.
4 for example, Section 7a of the paragraph). 1 (a). and a and b) of the Act) No. 64/1986 Coll., on Czech
commercial inspection, as amended by Act No. 22/1997 Coll. and Act No. 204/2002
SB.
4A) Government Regulation No. 190/2002 Coll., laying down the technical
the requirements for construction products CE known, as amended by Decree-Law No.
251/2003 Coll. and regulation of the Government No. 128/2004 Sb.
5) if it considers it necessary, the notified body may either issue an addition
to the original type-examination certificate, or request the submission of a new
the application of the exposing.
6) if it considers it necessary, the notified body may either issue an addition
to the original type-examination certificate, or request the submission of a new
the application of the exposing.
7) harmonised standard ČSN EN ISO 9003 is supplemented, if it is
necessary, of the special features of safety components.
8) the harmonised standard EN ISO 9001 is supplemented, if
necessary, of the special features of safety components.
9) the harmonised standard EN ISO 9003 is supplemented, if
necessary, the specificities related to the elevators.
10) the harmonised standard EN ISO 9001 is supplemented, if
necessary, of the special features of the lifts.
11) the harmonised standard EN ISO 9002 is supplemented, if
necessary, of the special features of the lifts.