K023316 - BEUDAMED

BEUDAMED

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1,201 results · 40ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 1k FDA registration 19 FDA classification 13 + More Filters

Country

United States 990 China 72 United Kingdom 24 South Korea 17 Belgium 15 Israel 12 Japan 10 Sweden 10 Canada 8 Switzerland 8 Taiwan 8 Italy 6 Poland 6 Germany 5 Netherlands 3 France 2 Philippines 2 Costa Rica 1 Mexico 1 Slovakia 1 + More Countries

Classification

FDA Class 2 888 FDA Class 1 177 FDA Unclassified 117 + More Classifications

FDA FEI Number

3023316 1k 1417592 1k 1220477 1k 3004111573 1k 1043214 1k 3001236905 1k 3005011024 1k 3002750084 1k 1721676 1k 3005747797 1k 3010041511 1k 1625425 996 3003058448 996 1000112877 993 1000112968 993 3003040625 993 1000123222 977 1047843 974 3003737899 972 2183744 958 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3023316 1k 1417592 1k 1220477 1k 3004111573 1k 1043214 1k 1423537 1k 3005011024 1k 1836161 1k 1721676 1k 3011137372 1k 3010041511 1k 1625425 996 2032098 996 1054241 993 1055236 993 2320762 993 1123071 977 1047843 974 9680794 972 2183744 958 + More FDA Registration Numbers

FDA K Number

K000085 1 K000098 1 K000369 1 K000387 1 K000392 1 K000432 1 K000441 1 K000455 1 K000657 1 K000704 1 K000714 1 K001098 1 K001175 1 K001449 1 K001572 1 K001690 1 K001853 1 K001965 1 K002180 1 K002213 1 + More FDA K Numbers

Dressing, Wound, Occlusive

FDA classification

FDA Class 1 ·Dressing, Wound, Occlusive

<1 …57 58 59 60 61 >

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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