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BEUDAMED

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1,841 results · 29ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 2k FDA Pre-Market Approval 139 FDA classification 6 + More Filters

Country

Taiwan 1k United States 320 Germany 20 Canada 9 Denmark 3 Belgium 1 Switzerland 1 United Kingdom 1 + More Countries

Classification

FDA Class 2 2k + More Classifications

FDA FEI Number

1000306431 607 3012421607 596 3026408938 577 3013298431 561 3011191255 558 3012494290 521 3012104670 513 3015997711 513 3003076831 512 1417592 509 3013557562 504 3007134734 503 3004145393 494 3018940143 494 3004009431 489 3015058854 485 3012725363 476 3005798905 466 3003741676 462 1220477 461 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

2029275 607 3012421607 596 3026408938 577 3013298431 561 3011191255 558 3012494290 521 3012104670 513 3015997711 513 2032112 512 1417592 509 3013557562 504 3007134734 503 3004145393 494 3018940143 494 3004009431 489 3015058854 485 3012725363 476 3005798905 466 3003741676 462 1220477 461 + More FDA Registration Numbers

FDA K Number

Den040004 1 K011598 1 K012306 1 K022510 1 K041558 1 K041853 1 K050129 1 K050496 1 K061104 1 K071462 1 K091038 1 K093006 1 K110286 1 K112782 1 K113831 1 K122028 1 K122246 1 K123980 1 K131096 1 K140782 1 + More FDA K Numbers

Wound Cleaner, Ultrasound

FDA classification

FDA Class 2 ·Wound Cleaner, Ultrasound

<1 …89 90 91 92 93 >

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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