# 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 3.1

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

The manufacturer shall lodge an application for assessment of his quality system 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)the address of the manufacturer's premises where the audits can be carried out;
(c)a written declaration that the same application has not been lodged with any other approved body;
(d)the identification of the PPE concerned;
(e)the documentation concerning the quality system.
Where the chosen body is not the body that has carried out the ... type-examination, the application shall also include the following:
(a)the technical documentation of the PPE described in Annex III;
(b)a copy of the ... type-examination certificate.

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Source: https://www.legislation.gov.uk/eur/2016/425/annex/VIII/division/CONFORMITY/division/3/division/3.1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2016-425/annex-VIII/division-CONFORMITY/division-3/division-3.1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.