JRA - BEUDAMED

BEUDAMED

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1,261 results · 19ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 1k FDA classification 24 FDA 510(k) 18 + More Filters

Country

United States 1k + More Countries

Classification

FDA Class 3 1k + More Classifications

FDA FEI Number

2124215 664 3009380063 640 1000165971 639 1028232 639 2017865 639 2182208 639 3002806500 639 3002806603 638 3002807576 638 3003120897 638 3003574398 638 3006705815 638 3008159616 638 3008377825 638 3013288201 638 3018094310 638 2648729 637 2649622 636 3004369318 635 3008973940 635 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

2124215 664 3009380063 640 1000165971 639 1028232 639 2017865 639 2032521 639 2182208 639 3002806603 639 3003120897 639 3006705815 638 3008159616 638 3008494315 638 3013288201 638 3018094310 638 9610139 638 9614453 638 2648729 637 2649622 636 3004209178 635 3008973940 635 + More FDA Registration Numbers

FDA K Number

K760999 1 K770678 1 K770986 1 K781916 1 K800491 1 K801553 1 K812701 1 K812799 1 K813547 1 K823041 1 K832731 1 K843124 1 K851034 1 K852950 1 K863736 1 + More FDA K Numbers

Optoacoustic Imaging System

FDA classification

FDA Class 3 ·Optoacoustic Imaging System

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

BEUDAMED

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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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