Akunah - BEUDAMED

BEUDAMED

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

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FDA 510(k) 1 FDA registration 1 + More Filters

Country

Australia 2 + More Countries

Classification

FDA Class 2 1 + More Classifications

FDA FEI Number

1000109969 1 1000115748 1 1000116130 1 1000116912 1 1000117423 1 1000122772 1 1000132370 1 1000139922 1 1000185293 1 1000207287 1 1000207387 1 1000220733 1 1000284313 1 1000306093 1 1000306340 1 1000314502 1 1000511585 1 1000514697 1 1000517638 1 1000525271 1 + More FDA FEI Numbers

Regulation

Us FDA 2 + More Regulations

FDA Registration Number

1000207387 1 1000314502 1 1032347 1 1043653 1 1045254 1 1047843 1 1054415 1 1056553 1 1057946 1 1061158 1 1063008 1 1064396 1 1064588 1 1064812 1 1066019 1 1066247 1 1125622 1 1220246 1 1226003 1 1226188 1 + More FDA Registration Numbers

Reflect

FDA registration

AKUNAH·1 product·🇦🇺 Australia

Akunah REFLECT

FDA Class 2 ·Radiology

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU MDR

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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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