MIV - BEUDAMED

BEUDAMED

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581 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA classification 581 + More Filters

Country

United States 581 + More Countries

Classification

FDA Class 2 275 FDA Class 1 255 FDA Not Classified 27 FDA Class 3 19 FDA Unclassified 5 + More Classifications

FDA FEI Number

3015550354 142 1119779 86 1000306617 85 3003750284 60 3022178699 56 1924669 55 3005670738 52 1524213 42 3006224287 42 2023365 36 3002806559 36 3003952975 35 2242436 34 2243471 33 1000122536 30 2245285 29 1318354 27 2022807 26 3002800697 25 3004530258 25 + More FDA FEI Numbers

Regulation

Us FDA 581 + More Regulations

FDA Registration Number

3015550354 142 1119779 86 2029372 85 3003750284 60 3022178699 56 1924669 55 3005360469 52 1524213 42 8010096 42 2023365 36 9610126 36 2032682 35 2242436 34 2243471 33 1528450 30 2245285 29 1318354 27 2022807 26 3002800697 25 3004530258 25 + More FDA Registration Numbers

FDA K Number

Den030002 1 Den030004 1 Den040003 1 Den060007 1 Den060008 1 Den070001 1 Den070004 1 Den070006 1 Den070013 1 Den100020 1 Den110001 1 Den110012 1 Den120008 1 Den120012 1 Den120013 1 Den120014 1 Den130003 1 Den130013 1 Den130032 1 Den130049 1 + More FDA K Numbers

Anti-Phospholipase A2 Receptor

FDA classification

FDA Class 2 ·Anti-Phospholipase A2 Receptor

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Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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