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BEUDAMED

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

Filters Classification: FDA Class 2 ×

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FDA 510(k) 819 FDA classification 2 + More Filters

Country

Finland 316 Japan 308 United States 112 Taiwan 37 Israel 17 China 13 South Korea 8 Ireland 3 France 2 Italy 2 Vietnam 2 United Kingdom 1 + More Countries

Classification

FDA Class 2 821 + More Classifications

FDA FEI Number

3009617712 368 3000126629 364 3009077524 314 3005877899 292 3018094310 292 1000114111 286 3004977335 271 3009196578 264 3001236277 259 3010703925 249 3008496839 246 3015276088 239 2011171 237 3010398867 231 3002808382 228 1047843 222 3001722928 213 3012494290 211 1000219637 207 2183744 203 + More FDA FEI Numbers

Regulation

Us FDA 821 + More Regulations

FDA Registration Number

3009617712 368 3000126629 364 3009077524 314 3005877899 292 3018094310 292 1054713 286 3004977335 271 3009196578 264 1649518 259 3010703925 249 3008496839 246 3015276088 239 2011171 237 3010398867 231 9614698 228 1047843 222 3001722928 213 3012494290 211 1058584 207 2183744 203 + More FDA Registration Numbers

FDA K Number

K023245 1 + More FDA K Numbers

PANPAC VAGINAL DILATORS

FDA Class 2 ·Obstetrics/Gynecology

<1 …38 39 40 41 42 >

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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