IVDR (In Vitro Diagnostics Regulation). IVDR is the regulatory basis for placing on the market, making available and putting into service in vitro diagnostic medical devices on the European market.

MDR (Medical Device Regulation) is a set of regulations that govern the clinical investigation, production and distribution of medical devices in Europe.

The certifications of IVDR and MDR products are available below to view and download.

If you need additional assistance on IVDR or MDR certificates, please contact Corporate_Quality_Regulatory@thermofisher.com

Legal EntitySite AddressCertificationExpiration DateScope StatementDocument
Phadia ABRapsgatan 7P
PO. Box 6460 751 37
Uppsala Sweden		(EU) 2017/746October 6, 2027In Vitro Diagnostic medical devices including reagents indended to be used for the confirmation/determination of allergies and asthmaEU QUALITY MANAGEMENT SYSTEM CERTIFICATE 39148
Phadia ABRapsgatan 7P
PO. Box 6460 751 37
Uppsala Sweden		(EU) 2017/746April 13, 2027In Vitro Diagnostic medical devices inlcuding reagents, calibrators, control materials and software, intended to be used for the confirmation/determination of allergies and asthma.EU QUALITY MANAGEMENT SYSTEM CERTIFICATE 38952
Phadia ABRapsgatan 7P
PO. Box 6460 751 37
Uppsala Sweden		(EU) 2017/746April 13, 2027In Vitro Diagnostic medical devices including reagents, calibrators and control materials, intended to be used for the determination of physiological markers for autoimmune diseases EU QUALITY MANAGEMENT SYSTEM CERTIFICATE 38953
Oxoid LimitedWade Road
Basingstoke, Hampshire, RG24 8PW
United Kingdom		 (EU) 2017/746November 28, 2027In Vitro Diagnostic medical devices intended for the determination of antimicrobial agent susceptibility and/or the qualative identification of infectious agents. EU QUALITY MANAGEMENT SYSTEM CERTIFICATE 742163 R000
Oxoid Deutschland GmBHAm Lippeglacis 4-8
Wesel 46483
Germany		(EU) 2017/746November 09, 2027Qualitative Selective media for the identification of bacterial infections. EU QUALITY MANAGEMENT SYSTEM CERTIFICATE 741817 R000
Thermo Electron LED GmbH Zweigniederlassung OsterodeAm Kalkberg, 37520 Osterode am Harz, Germany (EU) 2017/745November 19, 2028Device Group: B99 – Haematology and Haemotransfusion devices.  This centrifuge is intended for separation of blood into blood components using blood bags.  The blood components are intended to be used for human blood transfusion.  Clinical facilities and institutions are responsible for the process of human blood transfusion.  This intended use is limited to the associated rotors and components.TUV 713279377
Microgenics Corporation46500 Kato Road Fremont, CA 94538 USA(EU) 2017/746December 11, 2028Devices intended to be used for monitoring of levels of medicinal products, substances or biological components. Products of Class B and Class C.EU QMS HX 1061883-1
Nalge Nunc International Corporation, a part of Thermo Fisher Scientific Inc.75 Panorama Creek Drive Rochester, NY 14625 USA(EU) 2017/746January 16, 2029Class A Sterile devices, IVR 0803 Sterile specimen receptacles.BSI US-MF-000026915
Remel Europe LimitedRemel House Clipper Boulevard West Crossways Dartford Kent DA2 6PT United Kingdom(EU) 2017/746January 9, 2028Agglutination tests intended to be used to detect the presence of, or exposure to an infectious agent.BSI GB-MF-000016733
The Binding Site Group Ltd8 Calthorpe Road Edgbaston Birmingham B15 1QT United Kingdom(EU) 2017/746May 3, 2028Class D, C and B devices. Class C devices: Immunochemistry (Immunology) devices for in vitro detection of proteins as an aid in diagnosis and monitoring of monoclonal gammopathies, inflammatory conditions, kidney disease and haematological malignancies. Class B devices: Immunochemistry (Immunology) devices intended to be used for screening, determination or monitoring of physiological markers.BSI Single Registration Number Not Available