CHAPTER 3 CONFORMITY OF EQUIPMENT
1. EU-type examination is the part of a conformity assessment procedure...
2. EU-type examination shall be carried out by assessment of the...
3. The manufacturer shall lodge an application for EU-type examination with...
4. The notified body shall examine the technical documentation to assess...
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...
EU declaration of conformity (No Xxxx)
1. Apparatus model/Product (product, type, batch or serial number):
2. Name and address of the manufacturer or his authorised representative:...
3. This declaration of conformity is issued under the sole responsibility...
4. Object of the declaration (identification of apparatus allowing traceability; it...
5. The object of the declaration described above is in conformity...
6. References to the relevant harmonised standards used, including the date...
7. Where applicable, the notified body … (name, number) performed …...
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