BEUDAMED
    8 results · 14ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall × Status: Open, Classified × Clear all

    The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.

    FDA Recall
    Open, Classified ·FUJIFILM Healthcare Americas Corporation·Product code IZL·November 23, 2023

    SQ40S Blood Transfusion Filter

    FDA Recall
    Open, Classified ·GVS TM, Inc·Product code CAK·November 3, 2025

    Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025

    Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025

    Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025

    Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025

    Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025

    Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code FOS·May 2, 2025