Division 3.1 The manufacturer shall lodge an application for assessment of his quality system with the notified body of his choice.

The application shall include:

1. (a)

   the name and address of the manufacturer and, if the application is lodged by the authorised representative, his name and address as well;

2. (b)

   a written declaration that the same application has not been lodged with any F1other approved body;

3. (c)

   all relevant information for the subsystems or safety components approved under module B;

4. (d)

   the documentation concerning the quality system;

5. (e)

   the technical documentation of the approved type and a copy of F2the type examination certificate(s);

6. (f)

   details of the premises where the subsystem or the safety component is manufactured.