Paul-Ehrlich-Institut

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Measures Taken by Manufacturers

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.

RSS Feeds of the Paul-Ehrlich-Institut

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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Date Title
05.02.2015 Referenznummer PEI0005/15 (pdf in Englisch):
Korrektive Maßnahme zum IVD LABScreen Single Antigen Class I – Combi, Fa. One Lambda, Inc.
28.01.2015 Referenznummer PEI0004/15 (pdf in Englisch):
Korrektive Maßnahme zum IVD LABType HD DRB1 Typing Test, Fa. One Lambda, Inc.
14.01.2015 Referenznummer PEI0003/15 (pdf in Englisch):
Korrektive Maßnahme zum IVD Micro SSP DNA Typing Trays, Fa. One Lambda, Inc.
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