- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Directive 2014/34/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to equipment and protective systems intended for use in potentially explosive atmospheres (recast) (Text with EEA relevance)
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CRITERIA DETERMINING THE CLASSIFICATION OF EQUIPMENT-GROUPS INTO CATEGORIES
1. Common requirements for Equipment and protective systems
1.5. Requirements in respect of safety-related devices
1.5.1. Safety devices must function independently of any measurement and/or control...
1.5.2. In the event of a safety device failure, equipment and/or...
1.5.3. Emergency stop controls of safety devices must, as far as...
1.5.5. Requirements in respect of devices with a measuring function for...
1.5.6. Where necessary, it must be possible to check the reading...
1.5.7. The design of devices with a measuring function must incorporate...
1.6. Integration of safety requirements relating to the system
2. Supplementary requirements in respect of equipment
2.0. Requirements applicable to equipment in equipment-group I
2.1. Requirements applicable to equipment category 1 of equipment-group II
2.2. Requirements applicable to equipment category 2 of equipment-group II
2.2.1. Explosive atmospheres caused by gases, vapours or mists
2.2.2. Explosive atmospheres caused by air/dust mixtures
2.2.2.1. Equipment must be designed and constructed so that ignition of...
2.2.2.2. With regard to surface temperatures, requirement 2.1.2.3 applies.
2.2.2.3. With regard to protection against dust, requirement 2.1.2.2 applies.
2.2.2.4. With regard to the safe opening of equipment parts, requirement...
2.3. Requirements applicable to equipment category 3 of equipment-group II
3. Supplementary requirements in respect of protective systems
3.1.2. Protective systems designed to resist or contain explosions must be...
3.1.3. Accessories connected to protective systems must be capable of withstanding...
3.1.4. The reactions caused by pressure in peripheral equipment and connected...
3.1.8. Protective systems must be capable of being integrated into a...
1. EU-type examination is the part of a conformity assessment procedure...
2. EU-type examination shall be carried out with the examination of...
3. The manufacturer shall lodge an application for EU-type examination with...
5. The notified body shall draw up an evaluation report that...
6. Where the type meets the requirements of this Directive that...
7. The notified body shall keep itself apprised of any changes...
8. Each notified body shall inform its notifying authority concerning the...
9. The manufacturer shall keep a copy of the EU-type examination...
10. The manufacturer’s authorised representative may lodge the application referred to...
MODULE D: CONFORMITY TO TYPE BASED ON QUALITY ASSURANCE OF THE PRODUCTION PROCESS
1. Conformity to type based on quality assurance of the production...
3.1. The manufacturer shall lodge an application for assessment of his...
3.2. The quality system shall ensure that the products are in...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
4. Surveillance under the responsibility of the notified body
5. CE marking, EU declaration of conformity and attestation of conformity...
6. The manufacturer shall, for a period ending 10 years after...
7. Each notified body shall inform its notifying authority of quality...
MODULE E: CONFORMITY TO TYPE BASED ON PRODUCT QUALITY ASSURANCE
1. Conformity to type based on product quality assurance is that...
3.1. The manufacturer shall lodge an application for assessment of his...
3.2. The quality system shall ensure compliance of the products with...
3.3. The notified body shall assess the quality system to determine...
3.4. The manufacturer shall undertake to fulfil the obligations arising out...
3.5. The manufacturer shall keep the notified body that has approved...
4. Surveillance under the responsibility of the notified body
5. CE marking, EU declaration of conformity and attestation of conformity...
6. The manufacturer shall, for a period ending 10 years after...
7. Each notified body shall inform its notifying authority of quality...
EU DECLARATION OF CONFORMITY (No XXXX)
1. Product model/product (product, type, batch or serial number):
2. Name and address of the manufacturer and, where applicable, his...
3. This declaration of conformity is issued under the sole responsibility...
4. Object of the declaration (identification of product allowing traceability; it...
5. The object of the declaration described above is in conformity...
6. References to the relevant harmonised standards used or references to...
7. Where applicable, the notified body … (name, number) performed …...
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