Division 3 Application for supervised product checks at random intervals
United Kingdom
Before placing PPE on the market, the manufacturer shall lodge an application for supervised product checks at random intervals with a single F1approved body of his choice.
The application shall include the following:
- (a)
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 approved body;
- (c)
the identification of the PPE concerned.
Where the chosen body is not the body that has carried out the F2... type-examination, the application shall also include the following:
- (a)
the technical documentation described in Annex III;
- (b)
a copy of the ... type-examination certificate.
Annotations
Textual amendments
- F1
Word in Annex 7 para. 3 substituted (31.12.2020) by The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 35 para. 3(50)(b)(i); 2020 c. 1, Sch. 5 para. 1(1)
- F2
Word in Annex 7 para. 3 omitted (31.12.2020) by virtue of The Product Safety and Metrology etc. (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/696), reg. 1, Sch. 35 para. 3(50)(b)(ii); 2020 c. 1, Sch. 5 para. 1(1)