# Regulation (EU) 2016/425 of the European Parliament and of the Council of 9 March 2016 on personal protective equipment and repealing Council Directive 89/686/EEC (Text with EEA relevance), Division 3: Application for ... type-examination

Extent: E+W+S+N.I.

The manufacturer shall lodge an application for ... type-examination with a single approved body of his choice.
The application shall include:
(a)the name and address of the manufacturer and, if the application is lodged by the authorised representative, his name and address as well;
(b)a written declaration that the same application has not been lodged with any other approved body;
(c)the technical documentation described in Annex III;
(d)the specimen(s) of the PPE representative of the production envisaged. The approved body may request further specimens if needed for carrying out the test programme. For PPE produced in series where each item is adapted to fit an individual user, specimens shall be provided that are representative of the range of different users, and for PPE produced as a single unit to accommodate the special needs of an individual user, a basic model shall be provided.

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Source: https://www.legislation.gov.uk/eur/2016/425/annex/V/division/EU/division/3 (the official version)
Page: https://openlegislation.uk/eu-regulation-2016-425/annex-V/division-EU/division-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.