Division 2

The application includes:

• the name and address of the manufacturer and the name and address of the authorized representative if the application is lodged by the representative,

• the documentation described in Section 3 needed to assess the conformity of the representative sample of the production in question, hereinafter referred to as the ‘type’, with the requirements of this Directive. The applicant must make a ‘type’ available to the notified body. The notified body may request other samples as necessary,

• a written declaration that no application has been lodged with any other notified body for the same type.