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BEUDAMED

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1,101 results · 29ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 880 FDA Pre-Market Approval 147 FDA classification 74 + More Filters

Country

United States 656 China 299 Norway 48 Sweden 12 Türkiye 12 United Kingdom 10 Hong Kong 8 India 8 Taiwan 8 Germany 7 Ireland 6 Saudi Arabia 6 Japan 5 Switzerland 4 New Zealand 3 France 2 Australia 1 Belgium 1 Brazil 1 Denmark 1 + More Countries

Classification

FDA Class 2 1k + More Classifications

FDA FEI Number

3013557562 398 3012494290 350 3000126629 336 3012307300 334 3003076831 326 3001236905 302 3010605677 300 3013298431 300 3012636179 289 2011171 284 3005747797 279 1000138054 272 3009077524 265 1000219637 263 1928237 260 3016678045 257 3012104670 255 3015997711 255 3014579161 252 1721676 248 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3013557562 398 3012494290 350 3000126629 336 3012307300 334 2032112 326 1423537 302 3010605677 300 3013298431 300 3012636179 289 2011171 284 3011137372 279 1319639 272 3009077524 265 1058584 263 1928237 260 3016678045 257 3012104670 255 3015997711 255 3014579161 252 1721676 248 + More FDA Registration Numbers

FDA K Number

Den050001 1 Den090007 1 Den150049 1 Den160062 1 Den170064 1 Den180058 1 Den180062 1 Den190038 1 Den190043 1 Den190055 1 Den200010 1 Den200016 1 Den230025 1 Den230064 1 Den240048 1 K000646 1 K000697 1 K001069 1 K001146 1 K001714 1 + More FDA K Numbers

Radiology-Diagnostic Kit

FDA classification

FDA Class 2 ·Radiology-Diagnostic Kit

<1 …52 53 54 55 56 >

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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