BEUDAMED
    3 results · 26ms · 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 Adverse Event ×

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014

    INQUIRY STEERABLE CATH. 6F, 1110-6-25-L

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, IRVINE·Product code DRF·October 5, 2012

    RUSCH GREENSPEC FO HANDLE SMALL

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·May 18, 2015