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BEUDAMED

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341 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 212 FDA Pre-Market Approval 127 FDA classification 2 + More Filters

Country

United States 244 Canada 91 Germany 4 Australia 1 Costa Rica 1 + More Countries

Classification

FDA Class 2 341 + More Classifications

FDA FEI Number

1000113348 127 1000114111 127 1000138054 127 1000143606 127 1000158431 127 1000208827 127 1000219637 127 1000284313 127 1000306474 127 1000403400 127 1000517638 127 1000571342 127 1038814 127 1051786 127 1221108 127 1526534 127 1721113 127 1826555 127 1937223 127 2011171 127 + More FDA FEI Numbers

Regulation

Us FDA 341 + More Regulations

FDA Registration Number

1038814 127 1051786 127 1054713 127 1055916 127 1058584 127 1063285 127 1221108 127 1319639 127 1526534 127 1529041 127 1721113 127 1723170 127 1826555 127 1835830 127 1932738 127 1932898 127 1937223 127 2011171 127 2029299 127 2126677 127 + More FDA Registration Numbers

FDA K Number

K022398 1 K102336 1 K121186 1 K843282 1 K930419 1 + More FDA K Numbers

System, Nuclear Magnetic Resonance Imaging

FDA Pre-Market Approval

FDA Class 2 ·MAGNETOM

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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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