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BEUDAMED

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162 results · 22ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 161 FDA classification 1 + More Filters

Country

United States 64 France 40 Israel 14 Italy 12 Netherlands 12 Spain 8 Germany 3 China 2 South Korea 2 Canada 1 Finland 1 Ireland 1 Sweden 1 Switzerland 1 + More Countries

Classification

FDA Class 2 162 + More Classifications

FDA FEI Number

3002808227 76 3003258642 75 1000120578 74 1000244733 74 3001319476 74 3001431138 74 3002900199 74 3005028741 74 3005154439 74 3005695724 74 3006153348 74 3006515340 74 3006807694 74 3006850277 74 3007421149 74 3007491751 74 3007544634 74 3007712511 74 3008085016 74 3008108972 74 + More FDA FEI Numbers

Regulation

Us FDA 162 + More Regulations

FDA Registration Number

3002808227 76 1725006 75 1222993 74 2954354 74 3001431138 74 3004940677 74 3005028741 74 3005695724 74 3006153348 74 3006515340 74 3006807694 74 3006850277 74 3007421149 74 3007491751 74 3007544634 74 3007712511 74 3008085016 74 3008915316 74 3008929787 74 3009736547 74 + More FDA Registration Numbers

FDA K Number

K122389 1 K132949 1 K133739 1 K143040 1 K143554 1 K150035 1 K150720 1 K151296 1 K153568 1 K160329 1 K161043 1 K161199 1 K161458 1 K161551 1 K162512 1 K162828 1 K163176 1 K170637 1 K171052 1 K172004 1 + More FDA K Numbers

CAAS A-VALVE

FDA Class 2 ·Radiology

CAAS QCA 3D

FDA Class 2 ·Radiology

<1 …5 6 7 8 9 >

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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