BEUDAMED
    5 results · 38ms · 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 ×

    ONE TOUCH ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·August 4, 2009

    BIT, DRILL

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HTW·November 14, 2014

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 17, 2011

    EASYPUMP II ST 250-1, 5-S

    FDA Adverse Event
    Malfunction ·B. BRAUN PRODUCTION LTD.·Product code MEB·July 24, 2013

    BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN 83 UNITS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 16, 2026