IMLOGIX A DIV. OF MICROTERM - BEUDAMED

BEUDAMED

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1 results · 166ms · Sources: EU EUDAMED, US FDA

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United States 1 + More Countries

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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 1 + 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

IMLOGIX 1000 IMAGE DISPLAY SYSTEM

FDA Class 2 ·Radiology

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

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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

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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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