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BEUDAMED

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41 results · 17ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 39 FDA classification 2 + More Filters

Country

United States 39 Canada 1 Hong Kong 1 + More Countries

Classification

FDA Class 1 41 + More Classifications

FDA FEI Number

1417592 35 3007289408 34 1000118260 32 1000227792 32 1038963 32 3001084824 32 3001644142 32 3001751372 32 3002948288 32 3003154916 32 3003255844 32 3003340795 32 3003473196 32 3003965134 32 3004753358 32 3005273623 32 3005621808 32 3005869201 32 3006076154 32 3006513362 32 + More FDA FEI Numbers

Regulation

Us FDA 41 + More Regulations

FDA Registration Number

1417592 35 3007289408 34 3010131137 33 1038963 32 1062671 32 1424774 32 1932015 32 3003965134 32 3004753358 32 3005273623 32 3005621808 32 3005869201 32 3006513362 32 3006897996 32 3006943846 32 3007084590 32 3007865243 32 3008044484 32 3008852306 32 3009119999 32 + More FDA Registration Numbers

FDA K Number

K043526 1 K780283 1 K803141 1 K810110 1 K812904 1 K822059 1 K823394 1 K823819 1 K833084 1 K833406 1 K840617 1 K843780 1 K854341 1 K854554 1 K861073 1 K861074 1 K861075 1 K864092 1 K864966 1 K870404 1 + More FDA K Numbers

Radioimmunoassay, Estrone

FDA classification

FDA Class 1 ·Radioimmunoassay, Estrone

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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