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BEUDAMED

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241 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 240 FDA classification 1 + More Filters

Country

United States 197 Sweden 9 Taiwan 9 China 5 Israel 4 Netherlands 4 Canada 3 Germany 3 United Kingdom 3 Thailand 2 France 1 Japan 1 + More Countries

Classification

FDA Class 2 241 + More Classifications

FDA FEI Number

1417592 213 3010131137 205 1000306431 203 1043214 203 1000112877 202 1000112968 202 1000208624 202 3008770252 202 1000123222 201 1000136478 201 1220477 201 3000206435 201 3001236905 201 3003040625 201 1000114185 200 1000115048 200 1000117748 200 1000123971 200 1000127185 200 1000132370 200 + More FDA FEI Numbers

Regulation

Us FDA 241 + More Regulations

FDA Registration Number

1417592 213 3010131137 205 1043214 203 1054241 202 1055236 202 1060680 202 1423537 202 2029275 202 3008770252 202 1123071 201 1220477 201 1319660 201 2030624 201 2320762 201 1016427 200 1032347 200 1054811 200 1056350 200 1056553 200 1061927 200 + More FDA Registration Numbers

FDA K Number

K000098 1 K002767 1 K002915 1 K010117 1 K010694 1 K010727 1 K010785 1 K011078 1 K011208 1 K011863 1 K012041 1 K014277 1 K021608 1 K022754 1 K022880 1 K023154 1 K023682 1 K024107 1 K031812 1 K032125 1 + More FDA K Numbers

Clamp, Vascular

FDA classification

FDA Class 2 ·Clamp, Vascular

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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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