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BEUDAMED

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

Filters Classification: FDA Class 1 ×

Filter by

FDA 510(k) 153 FDA classification 108 + More Filters

Country

United States 232 China 21 Canada 3 Taiwan 3 United Kingdom 2 + More Countries

Classification

FDA Class 1 261 + More Classifications

FDA FEI Number

1417592 122 2648727 112 3013557562 112 3004824601 111 3004134948 110 3007208013 100 1000604079 97 3004365956 97 3005273623 97 3010131137 97 3010220595 96 3012316249 91 3012494290 91 3004727093 90 3014167550 90 3016746538 90 1000374126 89 1314417 89 1824226 89 1832562 89 + More FDA FEI Numbers

Regulation

Us FDA 261 + More Regulations

FDA Registration Number

1417592 122 2648727 112 3013557562 112 3004824601 111 3004134948 110 3007208013 100 1000604079 97 3004365956 97 3005273623 97 3010131137 97 3010220595 96 3012316249 91 3012494290 91 3004727093 90 3014167550 90 3016746538 90 1218704 89 1314417 89 1824226 89 1832562 89 + More FDA Registration Numbers

FDA K Number

K012320 1 K013282 1 K013304 1 K013866 1 K013919 1 K022067 1 K023969 1 K050656 1 K070340 1 K071269 1 K760456 1 K760777 1 K760993 1 K761167 1 K770300 1 K770354 1 K770581 1 K770593 1 K770670 1 K771013 1 + More FDA K Numbers

General Purpose Reagent

FDA classification

FDA Class 1 ·General Purpose Reagent

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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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