The new IVDR, and resulting recommendations from leading European Life Science Organizations, provide more clarity on product types that may be classified as in-vitro diagnostic medical devices, which has led to some changes in our IVD product portfolio.Įppendorf continues to offer centrifuges in two versions: An EU-IVD compliant version for diagnostic applications (affixed with the CE IVD mark according to the EU In Vitro Diagnostics Regulation (IVDR) 2017/746), and a General Lab Product version for research applications.Įppendorf pipettes, pipette tips and tubes affixed with the CE IVD mark are discontinued in May 2022.
Since May 2022, the EU IVD Regulation (IVDR) 2017/746 replaces the IVD Directive 98/79/EC under which a variety of Eppendorf products were registered as IVD products.
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