The Paul-Ehrlich-Institut publishes notifications made in accordance with Article 84 of the EU Regulation on In Vitro Diagnostics (IVDR) on this page.
Customer information contains details such as information from manufacturers about independently performed recalls of medical devices.
Current customer information (measures taken by manufacturers) can also be accessed via subscription to our RSS feed.
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Note: The customer information available on this page has been compiled by manufacturers, their authorised representatives, or medical device importers. The specified companies are responsible for the content of the customer information.
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