K953200 - BEUDAMED

BEUDAMED

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5,901 results · 40ms · Sources: EU EUDAMED, US FDA

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FDA Pre-Market Approval 4k FDA 510(k) 2k FDA registration 23 FDA classification 14 FDA UDI 1 + More Filters

Country

United States 6k Japan 52 Ireland 43 China 21 Canada 18 Israel 15 Germany 11 Netherlands 9 Sweden 5 France 4 Denmark 3 Switzerland 3 South Africa 1 Taiwan 1 United Kingdom 1 + More Countries

Classification

FDA Class 3 4k FDA Class 2 2k FDA Class 1 9 + More Classifications

FDA FEI Number

3001452571 6k 3002807314 6k 2011171 6k 1000121056 5k 1820334 4k 3015453963 4k 3016678045 4k 3002806434 4k 3009380063 3k 3000206435 3k 1016427 3k 1000116158 3k 2124215 2k 3001451463 2k 3002095335 2k 3002806565 2k 3010273872 2k 1721676 2k 3006950086 2k 3008114965 2k + More FDA FEI Numbers

Regulation

Us FDA 6k + More Regulations

FDA Registration Number

2953200 6k 3002807314 6k 2011171 6k 1000121056 5k 1225687 5k 1820334 4k 3015453963 4k 3016678045 4k 9612164 4k 3009380063 3k 2030624 3k 1721676 3k 1016427 3k 2184009 3k 2124215 2k 2134265 2k 3010273872 2k 9681260 2k 3006950086 2k 3008114965 2k + More FDA Registration Numbers

FDA K Number

Den100026 1 K000004 1 K000011 1 K000185 1 K000254 1 K000313 1 K000598 1 K000677 1 K000715 1 K000817 1 K000824 1 K000849 1 K001033 1 K001078 1 K001122 1 K001135 1 K001136 1 K001139 1 K001198 1 K001251 1 + More FDA K Numbers

Introducer, Catheter

FDA classification

FDA Class 2 ·Introducer, Catheter

<1 …292 293 294 295 296 >

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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