K220423 - BEUDAMED

BEUDAMED

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141 results · 44ms · Sources: EU EUDAMED, US FDA

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FDA Pre-Market Approval 125 FDA registration 8 FDA classification 4 FDA 510(k) 3 FDA UDI 1 + More Filters

Country

United States 135 South Korea 4 China 2 + More Countries

Classification

FDA Class 3 126 FDA Class 2 6 + More Classifications

FDA FEI Number

1220477 128 1220423 127 3010605677 127 1000359047 126 1219930 126 1416980 126 2210968 126 2648623 126 2648650 126 3002545766 125 3002808269 125 3003702646 125 3004474407 125 3004661493 125 3007093114 125 3017102971 125 405 125 3012421607 4 1000113657 2 1000114111 2 + More FDA FEI Numbers

Regulation

Us FDA 141 + More Regulations

FDA Registration Number

1220477 128 1220423 127 3010605677 127 1000359047 126 1219930 126 1416980 126 2031637 126 2210968 125 2648623 125 2648650 125 3001980567 125 3003702646 125 3004661493 125 3007093114 125 3017102971 125 8043792 125 9610725 125 3012421607 4 1000113657 2 1000115322 2 + More FDA Registration Numbers

FDA K Number

K000204 1 K000454 1 K000678 1 K000739 1 K000796 1 K001439 1 K001491 1 K001777 1 K001923 1 K001928 1 K001970 1 K002157 1 K002425 1 K002580 1 K002983 1 K003449 1 K010011 1 K010039 1 K010075 1 K010364 1 + More FDA K Numbers

Wheelchair, Powered

FDA classification

FDA Class 2 ·Wheelchair, Powered

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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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