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BEUDAMED

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941 results · 30ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 930 FDA 510(k) 11 + More Filters

Country

United States 937 United Kingdom 2 Israel 1 Japan 1 + More Countries

Classification

FDA Class 3 941 + More Classifications

FDA FEI Number

3002807314 374 1317628 291 3012236936 287 1119279 279 1610287 279 1038833 266 3015456951 266 2183744 253 2124215 251 3002806565 190 1000121056 189 3002807111 187 3002807944 180 2011171 175 3001451463 170 3010155661 168 1119421 167 2648035 167 2648045 167 3001284430 167 + More FDA FEI Numbers

Regulation

Us FDA 941 + More Regulations

FDA Registration Number

3002807314 374 1313525 291 3012236936 287 1119279 279 1610287 279 1038833 266 3015456951 266 2183744 253 2124215 251 9681260 190 1000121056 189 3005941719 187 9681121 180 2011171 175 1225687 170 3010155661 168 1063199 167 1119421 167 2648035 167 2648045 167 + More FDA Registration Numbers

BALL TIP, MODEL #030-185

FDA Class 3 ·Cardiovascular

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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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