BEUDAMED
    6 results · 18ms · 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 Regulation: Us FDA ×

    FLEX-CUP PERCUSSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    API GERM TUBE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GAUZE PADS STERILE SINGLES

    FDA 510(k)
    FDA Unclassified ·Unknown

    HOMECHOICE PRO

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 24, 2014

    ALARIS PUMP MODULE

    FDA Adverse Event
    Other ·CAREFUSION CORP.·Product code FRN·November 3, 2010

    STAMEY SUPRAPUBIC KIT

    FDA Adverse Event
    Malfunction ·COOK MEDICAL·Product code KOB·December 26, 2012