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BEUDAMED

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1,221 results · 22ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 865 FDA classification 206 FDA Pre-Market Approval 150 + More Filters

Country

United States 1k China 28 United Kingdom 26 Canada 13 Germany 12 Hungary 5 Switzerland 5 Ireland 4 Israel 4 France 3 Australia 2 Cayman Islands 2 South Korea 2 Türkiye 2 Denmark 1 Italy 1 Jordan 1 Taiwan 1 + More Countries

Classification

FDA Class 2 1k + More Classifications

FDA FEI Number

3001236905 585 1643817 430 1928237 418 3009888344 398 1043214 380 3005011024 372 3015550354 368 1000112877 347 1000112968 345 1000512168 337 1000306617 317 3010131137 312 3035642068 309 2011171 304 3005747797 288 1030451 281 2246703 273 1000138054 272 2433012 268 3006191977 260 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

1423537 585 1643817 430 1928237 418 3009888344 398 1043214 380 3005011024 372 3015550354 368 1054241 347 1055236 345 1061124 337 2029372 317 3010131137 312 3035642068 309 2011171 304 3011137372 288 1030451 281 2246703 273 1319639 272 2433012 268 3006191977 260 + More FDA Registration Numbers

FDA K Number

Den050007 1 Den130010 1 Den160025 1 Den160032 1 Den220090 1 Den240025 1 K001129 1 K001587 1 K001879 1 K001940 1 K002049 1 K002803 1 K003873 1 K010288 1 K010420 1 K011015 1 K011055 1 K011323 1 K011551 1 K011576 1 + More FDA K Numbers

Radiographic Contrast Tray

FDA classification

FDA Class 2 ·Radiographic Contrast Tray

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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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