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BEUDAMED

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

Filters Classification: FDA Class 2 ×

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FDA 510(k) 166 FDA Pre-Market Approval 12 FDA classification 3 + More Filters

Country

United States 124 Taiwan 26 China 16 Italy 7 South Korea 4 Austria 1 Canada 1 France 1 Switzerland 1 + More Countries

Classification

FDA Class 2 181 + More Classifications

FDA FEI Number

1000306431 77 1000114111 75 3013298431 67 3002808269 64 3004464325 60 3003058448 59 2936485 58 3008812560 57 3009417901 57 3002807305 55 1828288 54 3000270450 54 3002807692 54 3004975279 54 3010287737 54 3008693672 53 3008868758 53 3012636179 53 3015212339 53 3015440604 53 + More FDA FEI Numbers

Regulation

Us FDA 181 + More Regulations

FDA Registration Number

1054713 75 2029275 74 3013298431 67 8043792 63 3004464325 60 2032098 59 2936485 58 3008812560 58 3009417901 57 1828288 54 3000270450 54 3008693672 54 3010287737 54 8030965 54 3006540014 53 3008868758 53 3012636179 53 3015212339 53 3015440604 53 3023852420 53 + More FDA Registration Numbers

FDA K Number

K032117 1 K032607 1 K042434 1 K043408 1 K060270 1 K060274 1 K072030 1 K072146 1 K073678 1 K080220 1 K080761 1 K082532 1 K082649 1 K083569 1 K091227 1 K091252 1 K091331 1 K110881 1 K111290 1 K112188 1 + More FDA K Numbers

Drill, Bone, Powered

FDA classification

FDA Class 2 ·Drill, Bone, Powered

<1 …6 7 8 9 10 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

A better medical device search engine by OpenRegulatory.

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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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