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EC TYPE EXAMINATION (MODULE B) No. MED141323CS/001This is to certify, that RINA, specified as Notified Body N 0474 by the Italian \"Ministero delle Infrastrutture e dei Trasporti Direzione Generale
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Manufacturers of certain categories of products that fall under the scope of EU regulations may need to undergo Annex V EU Type-Examination to ensure compliance with safety and performance requirements.
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Annex V EU type-examination is a procedure that evaluates the conformity of a product to the relevant European Union legislation, ensuring that it meets the required health, safety, and environmental protection standards before being placed on the market.
Manufacturers or their authorized representatives who intend to market products covered by EU directives are required to file Annex V EU type-examination.
To fill out Annex V EU type-examination, the applicant must provide detailed information about the product, including its technical specifications, design, manufacturing processes, and relevant test reports to demonstrate compliance with applicable standards.
The purpose of Annex V EU type-examination is to ensure that products are assessed for compliance with EU regulations, thus protecting consumers, public safety, and the environment by preventing non-compliant products from entering the market.
The information that must be reported on Annex V EU type-examination includes product identification, manufacturer details, technical documentation, test results, and declarations of conformity.
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