K030973 - BEUDAMED

BEUDAMED

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261 results · 40ms · Sources: EU EUDAMED, US FDA

Filter by

FDA 510(k) 242 FDA registration 12 FDA classification 7 + More Filters

Country

United States 250 Switzerland 4 New Zealand 2 United Kingdom 2 Brazil 1 Germany 1 India 1 + More Countries

Classification

FDA Class 1 243 FDA Class 2 6 + More Classifications

FDA FEI Number

1417592 247 3005747797 245 1000112877 243 1000112968 243 1000115048 243 1000124817 243 1000136191 243 1000160162 243 1000307733 243 1000405819 243 1000508235 243 1000525271 243 1032347 243 1043214 243 1421101 243 1527821 243 1720747 243 1926681 243 1928237 243 2434839 243 + More FDA FEI Numbers

Regulation

Us FDA 261 + More Regulations

FDA Registration Number

1417592 247 3011137372 245 1032347 243 1043214 243 1054241 243 1055236 243 1057946 243 1058726 243 1421101 243 1421879 243 1527821 243 1646747 243 1720747 243 1836161 243 1926681 243 1928237 243 2084346 243 2431166 243 2434839 243 2529846 243 + More FDA Registration Numbers

FDA K Number

K000053 1 K000126 1 K000401 1 K000794 1 K000814 1 K000831 1 K000973 1 K001064 1 K001067 1 K001085 1 K001213 1 K001308 1 K001688 1 K001708 1 K001770 1 K001842 1 K001930 1 K001995 1 K002036 1 K002080 1 + More FDA K Numbers

Forceps

FDA classification

FDA Class 1 ·Forceps

<1 …10 11 12 13 14 >

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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