K010908 - BEUDAMED

BEUDAMED

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4,361 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 4k FDA registration 145 FDA classification 44 FDA UDI 4 + More Filters

Country

United States 3k Germany 408 South Korea 117 China 65 Canada 36 Japan 36 Taiwan 36 Netherlands 34 Italy 29 Switzerland 25 United Kingdom 22 Brazil 18 Australia 14 Israel 14 Liechtenstein 13 France 10 India 9 Sweden 9 Greece 8 Türkiye 7 + More Countries

Classification

FDA Class 2 4k FDA Class 1 353 FDA Unclassified 103 + More Classifications

FDA FEI Number

3002718942 4k 3012421607 4k 3006066614 4k 3026297922 4k 3012187973 4k 2515379 4k 1410097 4k 2024312 4k 3002808289 4k 3012494290 4k 2183301 4k 1718912 4k 3008822460 4k 3009496224 4k 3004966444 4k 3000719964 3k 3008912871 3k 3003667632 3k 2411797 3k 3002807050 3k + More FDA FEI Numbers

Regulation

Us FDA 4k + More Regulations

FDA Registration Number

8010908 4k 3012421607 4k 3006066614 4k 3026297922 4k 3012187973 4k 2515379 4k 1410097 4k 2024312 4k 9612300 4k 3012494290 4k 2183301 4k 1718912 4k 3008822460 4k 3009496224 4k 3004966444 4k 2086043 3k 3008912871 3k 9681210 3k 2411797 3k 3002807050 3k + More FDA Registration Numbers

FDA K Number

K000078 1 K000169 1 K000173 1 K000189 1 K000211 1 K000213 1 K000269 1 K000311 1 K000346 1 K000357 1 K000376 1 K000384 1 K000393 1 K000426 1 K000436 1 K000439 1 K000529 1 K000530 1 K000588 1 K000591 1 + More FDA K Numbers

Accessories, Implant, Dental, Endosseous

FDA classification

FDA Class 1 ·Accessories, Implant, Dental, Endosseous

<1 …215 216 217 218 219 >

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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