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EU TYPE EXAMINATION CERTIFICATE PRODUCTION TYPE This is to certify that Lloyd\'s Register Nederland B.V., a Notified Body under the terms of: The Pressure Equipment Directive 2014/68/EU, did (in accordance
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How to fill out a notified body under

01
Contact a notified body in your country or region.
02
Submit the necessary documentation and information required by the notified body.
03
Participate in the conformity assessment process conducted by the notified body.
04
Address any non-conformities raised by the notified body.
05
Obtain the relevant certification or approval issued by the notified body.

Who needs a notified body under?

01
Manufacturers of certain products such as medical devices, machinery, personal protective equipment, and toys may need a notified body to assess their compliance with applicable regulations.
02
Organizations seeking to export products to countries within the European Union typically require a notified body to certify their products before market access.
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A notified body is an organization designated by a member state to assess the conformity of certain products before being placed on the market.
Manufacturers or their authorized representatives who want to market products that fall under specific directives are required to file with a notified body.
To fill out a notified body registration, manufacturers need to complete the relevant application forms provided by the notified body, including details about their product, quality management systems, and compliance with applicable standards.
The purpose of a notified body is to ensure that products comply with regulatory requirements and standards, thereby enhancing product safety and reliability.
Information required includes product specifications, technical documentation, evidence of compliance with relevant directives, and quality management processes.
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