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BEUDAMED

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541 results · 23ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 536 FDA Pre-Market Approval 3 FDA classification 2 + More Filters

Country

Taiwan 354 United States 126 Canada 26 China 21 Netherlands 6 France 2 Finland 1 India 1 Ireland 1 Israel 1 Japan 1 United Kingdom 1 + More Countries

Classification

FDA Class 2 541 + More Classifications

FDA FEI Number

3009617712 222 1000306431 156 3012421607 146 3014279513 142 3002806559 141 3000126629 136 3026408938 136 3013298431 134 3011191255 128 3004009431 125 3012494290 125 1417592 124 3009077524 122 3003076831 121 3012104670 121 3015997711 121 3011989923 118 3012725363 117 3018094310 117 3018940143 116 + More FDA FEI Numbers

Regulation

Us FDA 541 + More Regulations

FDA Registration Number

3009617712 223 2029275 156 3012421607 146 3014279513 143 9610126 140 3000126629 136 3026408938 136 3013298431 134 3011191255 128 3004009431 125 3012494290 125 1417592 124 3009077524 122 2032112 121 3012104670 121 3015997711 121 3011989923 119 3012725363 117 3018094310 117 3018940143 116 + More FDA Registration Numbers

FDA K Number

K020548 1 K030329 1 K053531 1 K070708 1 K073604 1 K080167 1 K083373 1 K121951 1 K123379 1 K131244 1 K132058 1 K132249 1 K140842 1 K140859 1 K152422 1 K173122 1 K173495 1 K181233 1 K182423 1 K220456 1 + More FDA K Numbers

CO2 Laser Machine (Lume)

FDA Class 2 ·General, Plastic Surgery

<1 …24 25 26 27 28 >

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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