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BEUDAMED

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2,061 results · 19ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 2k FDA 510(k) 266 FDA classification 13 + More Filters

Country

United States 2k Netherlands 3 Israel 1 + More Countries

Classification

FDA Class 3 2k + More Classifications

FDA FEI Number

1721676 797 2011171 638 3002807314 630 1450662 557 1818910 545 3009380063 538 3004748528 536 3002807310 513 3007963827 513 3013055499 513 1526534 485 1220477 457 3010132111 453 3002808269 451 1218882 447 1000220733 439 3002807036 439 1828464 438 3002854251 438 3005061536 438 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

1721676 797 2011171 638 3002807314 630 1450662 557 1818910 545 3009380063 538 3004748528 536 3002807310 513 3007963827 513 3013055499 513 1526534 485 1220477 457 3010132111 453 8043792 451 1218882 447 1822565 439 3010173425 439 1828464 438 3005061536 438 3006356043 438 + More FDA Registration Numbers

FAST-PATCH

FDA Class 3 ·Cardiovascular

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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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