345/2016 Sb.
GOVERNMENT REGULATION
of 5 April 2004. October 2016
of the ship's rigging
Government orders under section 4, § 5 para. 1 and 2, § 6 (1). 2 and 3, § 7, § 8
paragraph. 2 and 4, section 11, section 12 paragraph 1. 1, § 15 para. 2, § 23 para. 3, § 41 para.
1 and § 50 para. 5 of law No. 90/2016 Coll., on conformity assessment provided for
products made available on the market:
§ 1
The subject of the edit
This regulation incorporates the relevant provision of the European Union "^ 1") and modifies the
and) technical requirements for gear
(b) conformity assessment) method of ship's equipment
(c)) the conditions and the rules for drawing up the EU Declaration of conformity and the
placement marks of conformity,
(d)) to the activities of operators details and notified bodies
and
e) formal defects, the neodstranění enables the supervisory authority
decide to adopt the appropriate protective measures.
§ 2
Product designed for conformity assessment
The product, which assesses conformity pursuant to this regulation, is shipping
equipment that is or is to be placed on board the ship and that is
listed in the directly applicable European Union legislation governing
requirements for the design, execution, and the location of the ship's equipment and test
standards for rigging.
§ 3
Technical requirements and conformity assessment
(1) the technical requirements of the gear set out in international agreements,
decisions and other acts of the International Maritime Organization and test standards
(hereinafter referred to as "international"). International regulations that apply to
apply the product, provides a directly applicable regulation in the European Union
governing the requirements for the design, execution, and the location of the ship's equipment and
testing standards for rigging.
(2) the fulfilment of the technical requirements referred to in paragraph 1 shall be determined procedures
According to the test standards and conformity assessment procedures set out in annex
No 1 to this regulation.
§ 4
The retention period for technical documentation
Technical documentation retention period corresponds to the time of the expected
life of the product, however, shall not be less than 10 years from the
the conformity of the product.
§ 5
Information, contact and identification details and safety information
to accompany the product
(1) the information and identification data on the product type number, are
batch or serial number or other indication enabling the unique
identification of the product.
(2) Identification and contact information are the name or registered
trademark and delivery address of the manufacturer or the importer.
(3) part of the instructions and safety information accompanying
the product are also provided for international documents.
§ 6
Time identification of economic operators
The period during which economic operators on request of the competent authorities
surveillance identifies the economic operator who has supplied them with a product or
which the product delivered corresponds to the time of the expected life of the product
specified by the manufacturer but shall not be less than 10 years from the
the conformity of the product.
§ 7
EU Declaration of conformity
(1) the EU Declaration of conformity shall be drawn up and copies thereof shall be attached to the
all the products.
(2) the retention period for EU Declaration of conformity corresponds to the time of the expected
life of the product by the manufacturer, must not be less than 10 years
from the location of the mark of conformity of the product.
§ 8
The rules for the affixing conformity marks
(1) on the product or product with a product that meets the technical
requirements and which has been meeting these requirements is verified according to
testing standards and conformity assessment procedure shall be placed mark of conformity,
the graphic design is reproduced in annex 2 to this regulation.
(2) the mark of conformity shall be included also in the software, if this is
equipment included with the product.
(3) If due to the nature of the product it is not possible to place a mark of conformity
directly to the product or to its data plate, place the mark of conformity on
the packaging of the product and of the documents accompanying it.
(4) for the mark of conformity shall indicate the year in which the mark of conformity on
the product is located.
§ 9
Formal defects
The formal lack of, which allows neodstranění of the supervisory authority
decide to adopt the appropriate protective measures, is the lack of
consisting in the fact that
and) mark of conformity has not been located or placed in contravention of this
by regulation,
(b)) the EU Declaration of conformity has not been drawn up or has not been drawn up
correctly,
(c)) copy of the EU Declaration of conformity has not been provided to the operator of a ship, on the
which is or is to be located, or the product
(d) the technical documentation was drawn up), is unavailable or
is incomplete.
§ 10
Requirements for notified bodies
(1) technical resources and staffing of the notified body
are in accordance with the
and Czech technical standard) EN ISO/IEC 17025 (01 5253) conformity assessment
-General requirements for the competence of testing and calibration
laboratories and
(b)) the Czech technical standard CSN EN ISO/IEC 17065 (01 5256) Assessment
compliance-requirements for bodies certifikující the products, processes and services.
(2) the Czech technical standards referred to in paragraph 1 are accessible at a
the headquarters of the Ministry of transport.
§ 11
Transitional provision
Until the entry into force of the regulation directly applicable in the European Union
governing the requirements for the design, execution, and the location of the ship's equipment and
testing standards for rigging is
and products) under this Regulation shall be considered as marine equipment in accordance with
Government Regulation No. 266/2009 Coll., on technical requirements for maritime
the device, in the version in force before the date of entry into force of this regulation,
and
(b)) for the determination of technical requirements and procedures to demonstrate their
meet pursuant to section 3 of annex 1 to this regulation, shall apply the technical
requirements and procedures to demonstrate their performance referred to in government regulation
No 266/2009 Coll., on technical requirements for marine equipment,
the version in force before the date of entry into force of this regulation.
§ 12
Regulation (EEC)
Shall be repealed:
1. Government Regulation No. 266/2009 Coll., on technical requirements for maritime
device.
2. Government Regulation No. 113/2010 Coll., amending Decree-Law No.
266/2009 Coll., on technical requirements for marine equipment.
3. Government Regulation No. 228/2011 Coll., amending Decree-Law No.
266/2009 Coll., on technical requirements for marine equipment, as amended by
Government Regulation No. 113/2010 Sb.
4. Decree-Law No 335/2012 Coll., amending Decree-Law No.
266/2009 Coll., on technical requirements for marine equipment, as amended by
amended.
section 13 of the
The effectiveness of the
This Regulation shall enter into force on the fifteenth day following its publication.
Prime Minister:
Mgr. Sobotka in r.
Minister of transport:
Ing. Ťok in r.
Č. 1
THE CONFORMITY ASSESSMENT PROCEDURES
A. GENERAL RULES FOR CONFORMITY ASSESSMENT
1. to assess the product's conformity with the technical requirements shall apply
conformity assessment procedures (modules) by directly applicable legislation
The European Union relating to the requirements for the design, execution, and the location of the
the ship's rigging and testing standards for rigging.
2. where the conformity assessment of the product used (EU type-examination (module B)
Type), it shall apply, for each product before it is placed on the market also
module D (conformity to type based on quality assurance of the production
process), module E (conformity to type based on quality assurance
products) or module F (conformity to type based on product verification).
If the product is produced individually or in small quantities, can be used
module G (conformity based on unit verification).
3. the conformity assessment of the individual modules is carried out according to the procedure
laid down in part B of this annex.
B. CONFORMITY ASSESSMENT PROCEDURES ACCORDING TO INDIVIDUAL MODULES
1. the EU type-examination (module B)
1.1 EU type examination is the part of a conformity assessment procedure in which
the notified body shall examine the technical design of the ship's rigging and verifies and
confirm that the technical design meets the appropriate requirements of ship equipment.
1.2 the EU type examination may be carried out by one of the following ways
and the sample of the full examination of the product), which is representative of the
the planned production (production type);
(b) assessment of the adequacy of the technical design) the ship's equipment, on the basis
examination of the technical documentation and supporting evidence referred to in points 1.3 and
1.4 examination of samples of one or more significant part of the essential
parts of the product, representative of the production envisaged (the combination of
the production type and design type).
1.3 the Manufacturer lodges an application with a single notified body of his choice,
the EU type-examination request.
1.4 the request contains
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
the notified body;
(c)) the technical documentation. Technical documentation enables the assessment of the
the conformity of the marine equipment with the relevant requirements of the international and
contains an adequate analysis and assessment of the risk. The technical documentation
Specifies the applicable requirements and to the extent necessary for the assessment by
on the design, manufacture and operation of the ship's rigging. The technical documentation
It contains, where applicable, at least the following particulars
-a general description of the ship's equipment;
-conceptual design and manufacturing drawings and schemes of components, sub-assemblies and
circuits;
-descriptions and explanations necessary for the understanding of said drawings and
schemes and the operation of the ship's equipment;
-the list of requirements and testing standards that are applicable to the
the marine equipment in accordance with this regulation, together with a description
of the solutions adopted to meet these requirements;
-results of design calculations made and examinations and
-test reports;
(d) samples representative of the planned) production. The notified body may
request further samples if the test programme so requires;
e) supporting evidence for the adequacy of the technical design solution. These
supporting evidence refer to any documents that have been applied.
The supporting evidence shall include, if necessary, the results of the tests
carry out appropriate laboratory of the manufacturer, or by another testing laboratory on his
behalf and under his responsibility.
1.5. the notified body shall examine the ship's equipment technical documentation
and supporting evidence to assess the adequacy of the technical design of the boat
equipment.
1.6 the notified body for a sample of
a) verifies that the specimens have been manufactured in conformity with the technical documentation, and
identify the elements which have been designed in accordance with the applicable requirements and
testing standards, as well as the elements which have been designed without
applying the relevant provisions of those standards;
(b)) shall carry out appropriate examinations and tests in accordance with this regulation
or ensure their implementation and
(c)) agree with the manufacturer on the spot where the examinations and tests
performed.
1.7. the notified body shall draw up an evaluation report that records the
the activities carried out under points 1.5 and 1.6, 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 whole or in part, only with the
the consent of the manufacturer.
1.8 if the type meets the requirements of the international special prescription,
that applies to the rigging, the notified body shall issue a
the EU type-examination certificate to the manufacturer. The certificate shall contain the name and
address of the manufacturer, conclusions of the examination, conditions for its validity and the
the necessary data for identification of the approved type. The certificate may be
one or more annexes attached. The certificate and its annexes contain
all relevant information to allow evaluation of whether they are produced
products in accordance with the examined type and perform a check in operation.
1.9 If the type does not satisfy the applicable requirements of the international code,
the notified body shall refuse to issue a certificate of the EU type-examination certificate and shall inform the
the applicant, with the refusal of the refusal. If approved by the
the type is no longer in accordance with the applicable requirements, the notified body
will decide if further tests are needed or a new conformity assessment.
1.10. 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 marine equipment with
the requirements of the international or the conditions for validity of the certificate.
Such modifications require additional approval in the form of a supplement to the original
the EU type-examination certificate.
1.11. the notified body shall inform the Authority of the EU type-examination certificates
type or 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.
The notified body shall inform the other notified bodies of the EU certificates
type-examination or additions thereto which it has refused, withdrawn,
suspended or otherwise restricted, and, upon request, about the certificates or
additions thereto which it has issued.
The notified body shall, on request of the European Commission, the Member States and the
the other notified bodies of the EU type-examination a copy of the certificate or
their additions. Also, on request, shall transmit to the European Commission and the Member
States a copy of the technical documentation and the results of the examinations carried out.
To the expiry of the EU type-examination certificate stores
the notified body must a copy of the certificate, its annexes and additions, as well as
as well as the technical file including the documentation submitted by the manufacturer.
1.12. The manufacturer shall keep at the disposal of public authorities a copy of the
the EU type-examination certificate, its annexes and additions together with the
the technical documentation for the expected life of the concerned boat
equipment, but at least for a period of 10 years after the mark of conformity
located on the final manufactured product.
1.13 the manufacturer's authorised representative may lodge the application referred to in points
1.3 and 1.4 and fulfil the obligations laid down in points 1.9, 1.10 and second sentence
1.12 if the manufacturer's authorised representative established in the mandate.
2. conformity to type BASED on QUALITY ASSURANCE of the PRODUCTION PROCESS
(MODULE D)
2.1. the conformity to type based on quality assurance of the production process
is that part of a conformity assessment procedure, the manufacturer fulfils the obligations
laid down in points 2.2 and 2.5 and on its own responsibility and guarantees
declares that the rigging is in conformity with the type as described in the
the EU type-examination certificate and satisfies the requirements of the international
the regulation that applies to it.
2.2. the manufacturer shall operate an approved quality system for production, final product
inspection and testing of the products concerned as specified in point 2.3 and shall be subject to surveillance
According to section 2.4.
2.3. Quality System
2.3.1. the Manufacturer lodges an application with a notified body of his choice, the request for
assessment of his quality system for the ship's equipment.
2.3.2 request contains
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
the notified body;
(c)) all relevant information on the estimated shipping category
equipment;
(d)) the documentation concerning the quality system, and
e) technical documentation of the approved type and a copy of the certificate of the EU
type-examination.
2.3.3 the quality system ensures conformity of the products with the type as described in the
the EU type-examination certificate and with the requirements of the international code,
that applies to them.
2.3.4. All the elements, requirements and provisions adopted by the manufacturer are
systematically and properly documented in the form of written policies, procedures
and instructions. The quality system documentation allow uniform interpretation
programmes, plans, manuals and records relating to quality.
2.3.5. the quality system documentation shall contain in particular an adequate description of
and) objectives in terms of quality and the organizational structure, responsibilities and
powers of the management with regard to product quality;
(b)) to the respective techniques, processes and systematic actions that are
used in the manufacture, control and quality assurance;
(c)) the examination and tests that will be carried out before, during
and after manufacture, the frequency with which;
d) inspection reports and test data, calibration data,
qualification reports on the personnel concerned, and other quality records
and
(e)) the means of monitoring the achievement of the required quality
products and the effective operation of the quality system.
2.3.6 the notified body shall assess the quality system to determine whether the
satisfies the requirements of items 2.3.3 to 2.3.5. Persons who, on behalf of the
the notified body shall carry out an assessment of the quality system, (hereinafter referred to as
"audit team") must have the necessary experience with systems management
quality and at least one Member must have the necessary experience with the
evaluation in the relevant area of the ship's equipment and technology assessment
the ship's equipment and knowledge of the applicable requirements of the international
prescription. The audit includes an assessment visit to the premises of the
manufacturer. The auditing team shall review the technical documentation referred to in
point 2.3.2 (b). (e)), in order to verify
the manufacturer's ability to identify the relevant requirements of the international
and carry out the necessary examination to ensure compliance of the product with the following
requirements. The conclusions of the audit, including the reasons therefor shall be notified to the manufacturer.
2.3.7 process according to the manufacturer's quality system as approved and to
keep, so that it remains adequate and efficient.
2.3.8. The manufacturer shall inform the notified body that has approved the system
quality, of any intended change of the quality system. The notified body
will examine the proposed changes and decide whether the modified quality system will also
continue to meet the requirements of items 2.3.3 to 2.3.5, or whether it should be
the new assessment. The notified body shall notify the manufacturer, the conclusions of its
the review, including the reasons therefor.
2.4 the Surveillance of the notified body
2.4.1. The purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations
arising out of the approved quality system. For the purpose of assessment will allow
the manufacturer to the notified body access to the places of manufacture,
inspection, testing and storage and must provide it with all necessary
information, in particular
the quality system documentation);
(b) protocols on the checks), test data, calibration data,
qualification reports of the personnel concerned, and other quality records.
2.4.2. The notified body must periodically carry out audits to make sure that the
manufacturer maintains and applies the quality system and shall provide the manufacturer detail about
audit.
2.4.3. In addition, the notified body may pay the manufacturer unannounced
visits, with the exception of cases in which such visits are subject to the
restrictions under other legislation. During such visits the
the notified body must, if necessary, carry out or have carried out tests
products, in order to verify that the quality system is functioning correctly. The notified body
provide the manufacturer with a visit report and, if they were
the tests carried out.
2.5. The manufacturer shall affix the mark of conformity and the identification number of the notified
body referred to in point 2.3.1 on each individual product that is
in conformity with the type as described in the EU type-examination certificate and satisfies the
the relevant requirements of the international code. The manufacturer shall establish for each
product model and a written declaration of conformity for a period of the expected life of the
the concerned ship's rigging, but at least for a period of 10 years after the
conformity mark affixed to the final manufactured product, it must, for
the need for public authorities. In the Declaration of conformity is the listed model
the ship's equipment, for which it has been drawn up. A copy of the Declaration of conformity
at the request of the relevant authorities.
2.6. The manufacturer shall keep available for public authorities for
the expected life of the concerned boat kits, at least for a period of 10
years after it was placed on the conformity mark last manufactured product
and) documentation described in section 2.3.2;
(b)) the amendments approved in accordance with section 2.3.8. and
(c)) the conclusions and reports of the notified body referred to in points 2.3.8,
2.4.2 and 2.4.3.
2.7. the notified body shall inform the Office of quality system approvals,
which it has issued or withdrawn, and shall, periodically or upon request, make available to the authority
the list of quality system approvals refused, suspended or otherwise
restricted. The notified body shall inform the other notified bodies of the
quality system approvals which it has refused, suspended, withdrawn or otherwise
restricted, and, upon the request of quality system approvals which it has issued.
2.8. The manufacturer's obligations set out in sections 2.3.1, 2.3.2, 2.3.8, 2.5 and
2.6 can be on his behalf and under his responsibility fulfilled his
authorised representative, if the producer on behalf of the authorised
a representative of the set.
3. conformity to TYPE BASED on PRODUCT QUALITY ASSURANCE (module E)
3.1 conformity to type based on product quality assurance is the
part of a conformity assessment procedure, the manufacturer fulfils the obligations
laid down in points 3.2 and 3.5, and on its own responsibility and guarantees
declares that the rigging is in conformity with the type as described in the
the EU type-examination certificate and satisfies the requirements of the international
the regulation that applies to it.
3.2. the manufacturer shall operate an approved quality system for final inspection and
testing of the products concerned as specified in point 3.3 and is subject to surveillance as specified in point
3.4.
3.3. Quality System
3.3.1. the manufacturer lodges an application with a notified body of his choice, the request for
assessment of his quality system for the ship's equipment.
3.3.2 application contains
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
the notified body;
(c)) all relevant information on the estimated shipping category
equipment;
(d)) the documentation concerning the quality system, and
e) technical documentation of the approved type and a copy of the certificate of the EU
type-examination.
3.3.3 the quality system ensures conformity of the products with the type as described in the
the EU type-examination certificate and with the applicable requirements of the international
prescription. All the elements, requirements and provisions adopted by the manufacturer are
systematically and properly documented in the form of written policies, procedures
and instructions. The quality system documentation allow uniform interpretation
programmes, plans, manuals and records relating to quality.
3.3.4 quality system documentation shall contain in particular an adequate description of
and) objectives in terms of quality and the organizational structure, responsibilities and
powers of the management with regard to product quality;
(b)) the examination and tests that will be carried out after manufacture;
c) inspection reports and test data, calibration data,
qualification reports on the personnel concerned, and other quality records
and
(d)) the means of monitoring the effective operation of the system
the quality.
3.3.5 the notified body shall assess the quality system to determine whether the
satisfies the requirements referred to in section 3.3.3 and 3.3.4, the auditing team shall have
experience in quality management systems, and at least one Member must have
with experience of evaluation in the relevant areas of the ship's equipment and evaluation
the technology of ship's equipment concerned, and knowledge of the applicable requirements
the international code. The audit includes an assessment visit to the premises of the
the premises of the manufacturer. The auditing team shall review the technical documentation
listed in section 3.3.2 (b). (e)), to verify the manufacturer's ability to identify
the relevant requirements of the international legislation and to make the necessary
examination to ensure compliance of the product with these requirements.
The conclusions of the audit, including the reasons therefor shall be notified to the manufacturer.
3.3.6 shall follow the manufacturer's quality system as approved and to
keep, so that it remains adequate and efficient.
3.3.7 the manufacturer shall inform the notified body that has approved the system
quality, of any intended change of the quality system. The notified body
will examine the proposed changes and decide whether the modified quality system will also
still satisfy the requirements referred to in section 3.3.3 and 3.3.4, or whether it should be
the new assessment. The notified body shall notify the manufacturer, the conclusions of its
the review, including the reasons therefor.
3.4. the Supervision of the notified body
3.4.1. The purpose of surveillance is to make sure that the manufacturer duly fulfils the obligations
arising out of the approved quality system.
3.4.2 in order to allow the manufacturer to the notified body assessment access
to the places of manufacture, inspection, testing and storage, and
provide it with all necessary information, in particular
and quality and system documentation)
(b) protocols on the checks), test data, calibration data,
qualification reports of the personnel concerned, and other quality records.
3.4.3. The notified body must periodically carry out audits to make sure that the
manufacturer maintains and applies the quality system and shall provide the manufacturer detail about
audit.
3.4.4. Furthermore, the notified body may pay the manufacturer unannounced
visits, with the exception of cases in which such visits are subject to the
restrictions under other legislation. During such visits the
the notified body must, if necessary, carry out or have carried out tests
products, in order to verify that the quality system is functioning correctly. The notified body
provide the manufacturer with a visit report and, if they were
the tests carried out.
3.5 conformity marking and Declaration of conformity
3.5.1. The manufacturer shall affix the mark of conformity and the identification number of the notified
body referred to in point 3.3.1 on each individual product that is
in conformity with the type as described in the EU type-examination certificate and satisfies the
the relevant requirements of the international code.
3.5.2. The manufacturer shall establish for each product model a written declaration of
compliance and for the expected life of the concerned boat kits, at least
However, after a period of 10 years after the conformity mark affixed to the last
manufactured product, it shall keep at the disposal of public authorities. In
Declaration of conformity model boat kits is listed, for which it has been
drawn up. A copy of the Declaration of conformity on request to the competent
authorities.
3.6. The manufacturer shall keep available for public authorities for
the expected life of the concerned boat kits, at least for a period of 10
years after it was placed on the conformity mark last manufactured product
and) documentation as described in section 3.3.2;
(b)) approved changes according to section 3.3.7 and
(c)) the conclusions and reports of the notified body referred to in point 3.3.7,
3.4.3 and 3.4.4.
3.7. the notified body shall inform the Office of quality system approvals,
which it has issued or withdrawn, and shall, periodically or upon request, make available to the authority
the list of quality system approvals refused, suspended or otherwise
restricted.
3.8. the notified body shall inform the other notified bodies of the approvals
the quality system which it has refused, suspended or withdrawn, and, upon request,
quality system approvals which it has issued.
3.9. The manufacturer's obligations set out in sections 3.3.1, 3.3.2, 3.3.7, 3.5 and
3.6 can be on his behalf and under his responsibility fulfilled his
authorised representative, if the producer on behalf of the authorised
a representative of the set.
4. Conformity to type based on PRODUCT VERIFICATION (module F)
4.1 conformity to type based on product verification is the part of the procedure
conformity assessment, the manufacturer fulfils the obligations laid down in points
4.2 and 4.7, 4.6.1, and on his own responsibility, ensures and declares
that the products which have been subjected to the provisions of point 4.3 and 4.4,
identical to the type as described in the EU type-examination certificate and satisfy the
the requirements of the international code that applies to them.
4.2. the manufacturer shall take all measures necessary so that the manufacturing process and its
monitoring ensure conformity of the manufactured products with the approved type
as described in the EU type-examination certificate and with the requirements of the international
the legislation that applies to them.
4.3. the notified body chosen by the manufacturer, performs the appropriate
examinations and tests to check the conformity of the products with the approved type
as described in the EU type-examination certificate and with the applicable requirements
the international code.
4.4. the examinations and tests to check the conformity of the products with the appropriate
requirements shall be carried out either according to the manufacturer's choice, examination and testing of
each of the products referred to in point 4.5 or examination and testing of products on a
statistical basis as specified in point 4.6.
4.5 checking the conformity examination and testing of every product
4.5.1 all products shall be individually be in accordance with this
Regulation in order to verify conformity with the approved type as described in the
the EU type-examination certificate and with the applicable requirements of the international
prescription.
4.5.2. the notified body shall issue a certificate of conformity with regard to the carried out
examinations and tests and shall affix to each approved product or have it
affix its identification number.
4.5.3. The manufacturer shall keep the certificates of conformity available for the national authorities
Administration for the expected life of the concerned boat kits, at least
However, after a period of 10 years after the conformity mark affixed to the last
manufactured product.
4.6 statistical verification of conformity
4.6.1 the manufacturer shall take all measures necessary so that the manufacturing process and
its monitoring ensure the homogeneity of each produced the series, and
shall present his products for verification in the form of homogeneous batches.
4.6.2 from each series with the random sample. All products
in the sample shall be individually examined and be in accordance with this
Regulation in order to ensure their conformity with the relevant requirements of the
the international legislation and to determine whether the lot is accepted or
rejected.
4.6.3 If a lot is accepted, all products in the series for
approved, except for those products from the sample which were recorded
the disappointing results of the tests.
4.6.4. the notified body shall issue a certificate of conformity with regard to the carried out
examinations and tests and shall affix to each approved product or have it
affix its identification number.
4.6.5. The manufacturer shall keep the certificates of conformity at the disposal of the national authorities
Administration for the expected life of the concerned boat kits, at least
However, after a period of 10 years after the conformity mark affixed to the last
manufactured product.
4.6.6 If a lot is rejected, the notified body or the competent authority
shall take appropriate measures to prevent the placing on the market of the series. In
the event of frequent rejection of lots the notified body statistics
pause verification and take appropriate measures.
4.7 the conformity marking and Declaration of conformity
4.7.1. The manufacturer shall affix the mark of conformity and the identification number of the notified
body referred to in point 4.3 and 4.4 for each individual product, that
is in conformity with the approved type as described in the EU type-examination certificate
type satisfies the applicable requirements of the international.
4.7.2. The manufacturer shall establish for each product model a written declaration of
compliance and for the expected life of the concerned boat kits, at least
However, after a period of 10 years after the conformity mark affixed to the last
manufactured product, it shall keep at the disposal of public authorities. In
Declaration of conformity model boat kits is listed, for which it has been
drawn up.
4.7.3. A copy of the Declaration of conformity on request to the competent authorities
the State administration.
4.8 if the notified body agrees, the manufacturer of the notified
affix the identification number of the body during the
of the production process.
4.9. The manufacturer's obligations may be on his behalf and under his responsibility,
fulfilled by his authorised representative, if this manufacturer in the mandate
authorised representative established. Authorized representative cannot act
the manufacturer's obligations set out in points 4.2 and 4.6.1.
5. conformity based on UNIT VERIFICATION (module G)
5.1 conformity based on unit verification is
the conformity assessment procedure whereby the manufacturer fulfils the obligations laid down in
sections 5.2, 5.3, 5.4 and 5.8 and on its own responsibility and guarantees
declares that the product has been subjected to the provisions of points up to 5.5
5.7, is in conformity with the requirements of the international code that it
applies.
5.2. the manufacturer shall establish the technical documentation and make it available to
notified body referred to in point 5.5. Documentation allows you to
conformity of the product with the applicable requirements and contains the corresponding
analysis and assessment of risks. Technical documentation specifying its
requirements, and to the extent necessary for the assessment applies to the design, manufacture and
the operation of the product. The technical documentation shall include, if appropriate,
at least the following particulars
and a general description of the product);
b) conceptual design and manufacturing drawings and schemes of components, sub-assemblies and
circuits;
c) descriptions and explanations necessary for the understanding of those drawings and schemes
and operation of the product;
(d) a list of requirements and test) standards which are applicable to
the ship's equipment in accordance with this regulation, together with a description
of the solutions adopted to meet these requirements;
e) results of design calculations made and examinations and
f) test reports.
5.3. The manufacturer shall keep the technical documentation at the disposal of the national authorities
Administration for the expected life of the concerned boat kits, at least
However, after a period of 10 years after the conformity mark affixed to the last
manufactured product.
5.4. the manufacturer shall take all measures necessary so that the manufacturing process and its
monitoring ensure conformity of the manufactured product with the applicable requirements of the
the international code.
5.5. The notified body chosen by the manufacturer, it executes the corresponding
examinations and tests in accordance with this regulation, in order to verify whether the
the product complies with the relevant requirements of the international code.
5.6. the notified body shall issue a certificate of conformity with regard to the carried out
examinations and tests and approved product shall affix, or cause to be allowed
its identification number.
5.7. The manufacturer shall keep the certificates of conformity at the disposal of public authorities
for the expected life of the concerned boat kits, at least
period of 10 years after the mark of conformity affixed to the last made
product.
3.6 conformity marking and Declaration of conformity
5.8.1 the manufacturer shall affix the mark of conformity and the identification number of the notified
body referred to in point 5.5 on each product that satisfies the applicable
the requirements of international law.
5.8.2 the manufacturer shall draw up a written declaration of conformity for a period and the expected
the life of the marine equipment concerned, however, at least for a period of 10 years after the
was conformity mark affixed to the final manufactured product, it keeps
the disposal of the bodies of State administration. The Declaration of conformity is provided
product for which it has been drawn up. A copy of the Declaration of conformity on
request of the competent authorities.
The manufacturer's obligations set out in sections 5.2, 5.3 and 5.8 may be his
behalf and under his responsibility fulfilled by his authorised representative, if
the manufacturer's authorised representative established in the mandate.
Č. 2
MARK OF CONFORMITY
1. the conformity mark has the following form:
2. If the conformity mark is reduced or enlarged, must be preserved
the proportions given in the drawing referred to in paragraph 1. Individual
part of the mark of conformity must have the same vertical dimension, which may not be
less than 5 mm.
1) directive of the European Parliament and of the Council 90/EU of 22. July
2014 to a ship's rigging and repealing Council Directive 96/98/EC.
