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WAREHOUSE
BSI
This photo is from the organization's website.
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.
