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BEUDAMED

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5,721 results · 62ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 5k FDA Pre-Market Approval 332 FDA classification 162 + More Filters

Country

United States 4k China 433 Taiwan 203 Germany 83 Canada 74 Switzerland 65 Norway 48 Australia 45 United Kingdom 45 New Zealand 44 South Korea 36 Japan 33 Italy 31 France 27 Israel 24 Hong Kong 16 Ireland 15 India 10 Denmark 9 Finland 8 + More Countries

Classification

FDA Class 2 6k + More Classifications

FDA FEI Number

3000126629 2k 3001236277 2k 2011171 2k 1417592 2k 3013557562 2k 3009973336 2k 3020460367 2k 3018783526 2k 3023272766 2k 1000306431 2k 3003319165 2k 1216677 2k 3007603826 2k 3002807167 2k 3009156722 2k 2221819 2k 3001084824 2k 3004727093 2k 3012494290 2k 1220477 2k + More FDA FEI Numbers

Regulation

Us FDA 6k + More Regulations

FDA Registration Number

3000126629 2k 1649518 2k 2011171 2k 1417592 2k 3013557562 2k 3009973336 2k 3020460367 2k 3018783526 2k 3023272766 2k 2029275 2k 8043316 2k 1216677 2k 3007603826 2k 9610816 2k 3009156722 2k 2221819 2k 9680215 2k 3004727093 2k 3012494290 2k 1220477 2k + More FDA Registration Numbers

FDA K Number

Den000002 1 Den070001 1 Den070014 1 Den080006 1 Den080011 1 Den090008 1 Den130012 1 Den130016 1 Den140017 1 Den150005 1 Den150048 1 Den160047 1 Den160056 1 Den170072 1 Den180014 1 Den180032 1 Den180047 1 Den180057 1 Den180065 1 Den190026 1 + More FDA K Numbers

On-Body Injector

FDA classification

FDA Class 2 ·On-Body Injector

<1 …283 284 285 286 287 >

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

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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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