KIE - BEUDAMED

BEUDAMED

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1,341 results · 23ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 1k FDA classification 207 FDA Pre-Market Approval 83 + More Filters

Country

United States 830 Ireland 385 China 32 United Kingdom 23 Canada 22 Germany 12 Japan 11 Taiwan 7 Switzerland 4 France 3 Australia 2 Israel 2 Italy 2 South Korea 2 Jordan 1 Kenya 1 South Africa 1 Türkiye 1 + More Countries

Classification

FDA Class 2 1k + More Classifications

FDA FEI Number

3001236905 602 1643817 493 1928237 437 3009888344 412 1043214 407 3005011024 391 1000512168 384 1000112877 368 1000112968 366 2011171 355 1721676 343 3015550354 334 3010131137 333 3005747797 324 1000138054 319 3035642068 318 1000306617 312 3000206435 302 1018470 288 3013557562 285 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

1423537 602 1643817 493 1928237 437 3009888344 412 1043214 407 3005011024 391 1061124 384 1054241 368 1055236 366 2011171 355 1721676 343 3015550354 334 3010131137 333 3011137372 324 1319639 319 3035642068 318 2029372 312 2030624 302 1018470 288 3013557562 285 + 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

<1 …64 65 66 67 68 >

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

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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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