K032809 - BEUDAMED

BEUDAMED

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101 results · 20ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 97 FDA classification 4 + More Filters

Country

United States 88 Italy 3 South Korea 3 Switzerland 3 France 2 Germany 2 + More Countries

Classification

FDA Class 2 101 + More Classifications

FDA FEI Number

1000120613 99 1000219637 99 1317628 99 2020601 97 3000206435 97 3004106598 97 3004169154 97 3008717566 97 3009420598 97 1000125147 58 3018094310 58 1000118360 56 1000125732 56 1000518699 56 1000655158 56 1045254 55 1047843 55 1118193 55 1220246 55 2022994 55 + More FDA FEI Numbers

Regulation

Us FDA 101 + More Regulations

FDA Registration Number

1058584 99 1222928 99 1313525 99 2020601 97 2030624 97 2032809 97 3008717566 97 3009420598 97 3011423170 97 2028523 58 3018094310 58 1000655158 56 1045254 56 1047843 56 1118193 56 1220246 55 1645337 55 2022994 55 2027804 55 2030580 55 + More FDA Registration Numbers

FDA K Number

K000060 1 K000543 1 K000608 1 K001137 1 K001803 1 K001807 1 K001895 1 K002153 1 K002543 1 K002831 1 K003022 1 K003169 1 K003277 1 K003344 1 K003522 1 K004005 1 K010311 1 K010666 1 K010680 1 K012006 1 + More FDA K Numbers

Staple, Implantable

FDA classification

FDA Class 2 ·Staple, Implantable

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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