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BSI

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Het is nu tijd voor je MDR aanvraag

Medical device manufacturing is one of the most regulated components in which important quality systems and product requirements must be met. The regulatory requirements are intended to ensure consistent design, manufacture and marketing of medical devices that are safe and fit for the recommended purpose.

CE marking

BSI Netherlands is a Notified Body (identification number 2797). BSI assesses and certifies products for CE marking to ensure they meet the requirements of European directives and regulations. The European NANDO database contains all notified bodies designated by the EU Member States.

BSI

John M. Keynesplein 9
1066 EP
Amsterdam

Contact

+31 (0)20 346 07 81

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