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BEUDAMED

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361 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 327 FDA Pre-Market Approval 31 FDA classification 3 + More Filters

Country

United States 332 United Kingdom 9 Netherlands 7 Canada 6 China 5 Australia 1 Brazil 1 + More Countries

Classification

FDA Class 2 361 + More Classifications

FDA FEI Number

2432235 309 3006198300 309 1000136573 307 2517506 307 3002806559 307 1827821 282 2050012 282 1000305841 280 1220972 280 2050010 280 2250051 280 3000215862 280 3000308930 280 2020952 279 3002642396 276 3005333358 276 3010939897 276 3012963943 276 3002806560 275 3003610499 275 + More FDA FEI Numbers

Regulation

Us FDA 361 + More Regulations

FDA Registration Number

2432235 309 3006198300 309 1319681 307 2517506 307 9610126 307 1827821 282 2050012 282 1220972 280 1319808 280 2030861 280 2050010 280 2020952 279 2250051 276 3000308930 276 3002642396 276 3005333358 276 3010939897 276 3012963943 276 3003610499 275 3003795116 275 + More FDA Registration Numbers

FDA K Number

K000131 1 K000461 1 K001126 1 K001567 1 K002263 1 K002375 1 K003557 1 K010001 1 K010138 1 K010921 1 K011112 1 K011300 1 K011813 1 K012109 1 K012390 1 K012541 1 K013247 1 K014066 1 K014193 1 K020769 1 + More FDA K Numbers

Calibrators, Drug Specific

FDA classification

FDA Class 2 ·Calibrators, Drug Specific

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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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