KST - BEUDAMED

BEUDAMED

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1,981 results · 29ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 2k FDA classification 213 FDA Pre-Market Approval 104 + More Filters

Country

United States 2k China 104 Taiwan 49 United Kingdom 28 Canada 19 Germany 13 Israel 11 Australia 5 France 5 India 4 Ireland 4 Switzerland 4 South Korea 3 Argentina 2 Denmark 1 Finland 1 Iran 1 Italy 1 Jordan 1 South Africa 1 + More Countries

Classification

FDA Class 2 2k + More Classifications

FDA FEI Number

3001236905 724 1928237 538 2011171 524 1643817 515 1043214 453 3013557562 430 3015550354 430 3009888344 414 3005011024 413 3012307300 411 3012494290 411 1832216 398 1000512168 392 1000112877 391 1000112968 389 3005747797 367 3000206435 345 3010131137 337 3035642068 328 1000138054 324 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

1423537 724 1928237 538 2011171 524 1643817 515 1043214 453 3013557562 430 3015550354 430 3009888344 414 3005011024 413 3012307300 411 3012494290 411 1832216 398 1061124 392 1054241 391 1055236 389 3011137372 367 2030624 345 3010131137 337 3035642068 328 1319639 324 + More FDA Registration Numbers

FDA K Number

Den050007 1 Den130010 1 Den160025 1 Den160032 1 Den220090 1 Den240025 1 K001129 1 K001587 1 K001679 1 K001879 1 K001940 1 K002049 1 K002105 1 K002803 1 K003873 1 K010288 1 K010420 1 K010488 1 K011015 1 K011055 1 + More FDA K Numbers

Radiographic Contrast Tray

FDA classification

FDA Class 2 ·Radiographic Contrast Tray

<1 …96 97 98 99 100 >

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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