EIT - BEUDAMED

BEUDAMED

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1,121 results · 26ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 1k FDA Pre-Market Approval 83 FDA classification 4 + More Filters

Country

Italy 784 United States 233 Israel 51 Ireland 23 Germany 7 Canada 5 China 4 Australia 3 France 3 Argentina 2 Austria 2 Finland 1 Hong Kong 1 Iran 1 United Kingdom 1 + More Countries

Classification

FDA Class 2 1k + More Classifications

FDA FEI Number

1220477 325 3000215273 320 2183744 309 3002808269 309 3003015552 307 2011171 305 3018094310 297 2528981 274 1721676 270 1000138054 268 3001236277 265 1000136269 262 1018470 262 1928237 261 3013557562 260 1000219637 257 3002806603 256 3003477135 247 1000114111 245 3002807111 242 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

1220477 325 1423662 320 2183744 309 8043792 309 1424263 307 2011171 305 3018094310 297 2528981 274 1721676 270 1319639 268 1649518 265 1018470 262 2244478 262 1928237 261 3013557562 260 1058584 257 3002806603 256 3003477135 247 1054713 245 3005941719 242 + More FDA Registration Numbers

FDA K Number

Den070014 1 K001679 1 K010488 1 K013145 1 K013698 1 K023551 1 K060318 1 K071211 1 K071525 1 K071580 1 K080485 1 K093883 1 K760010 1 K760193 1 K770318 1 K771153 1 K772029 1 K780013 1 K780039 1 K780103 1 + More FDA K Numbers

Galaxy UNYCO System

FDA Class 2 ·Orthopedic

<1 …53 54 55 56 57 >

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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BEUDAMED

Rationale
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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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