K010916 - BEUDAMED

BEUDAMED

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4,461 results · 56ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 4k FDA classification 26 FDA registration 25 FDA Pre-Market Approval 13 FDA UDI 12 + More Filters

Country

United States 4k Germany 95 France 88 Switzerland 78 Taiwan 61 Italy 48 Canada 45 South Korea 43 Ireland 36 Israel 33 Australia 21 Belgium 18 China 17 India 13 United Kingdom 8 Brazil 6 Sweden 4 Austria 2 Malaysia 2 Denmark 1 + More Countries

Classification

FDA Class 2 4k FDA Class 1 209 + More Classifications

FDA FEI Number

3003569173 4k 1526534 4k 1818910 4k 1828464 4k 3004889950 4k 1450662 4k 3005061536 4k 3012217062 4k 3000215273 4k 3001049282 4k 3003128516 4k 1000306340 4k 3003015552 4k 3008868758 4k 3002808269 4k 3009888740 4k 3002907620 4k 3006017180 4k 3002807113 4k 1828288 4k + More FDA FEI Numbers

Regulation

Us FDA 4k + More Regulations

FDA Registration Number

8010916 4k 1526534 4k 1818910 4k 1828464 4k 3004889950 4k 3005061536 4k 1450662 4k 3012217062 4k 1423662 4k 2249615 4k 1226544 4k 1834331 4k 1424263 4k 3008868758 4k 8043792 4k 3009888740 4k 3002907620 4k 3006017180 4k 9681465 4k 1828288 4k + More FDA Registration Numbers

FDA K Number

K000083 1 K000091 1 K000113 1 K000172 1 K000207 1 K000209 1 K000232 1 K000246 1 K000254 1 K000306 1 K000319 1 K000321 1 K000334 1 K000335 1 K000521 1 K000538 1 K000575 1 K000590 1 K000666 1 K000682 1 + More FDA K Numbers

Orthopedic Manual Surgical Instrument

FDA classification

FDA Class 1 ·Orthopedic Manual Surgical Instrument

<1 …220 221 222 223 224 >

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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