BEUDAMED
    3 results · 27ms · 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 ×

    NATURAL-KNEE II CONGRUENT TIBIAL INSERT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JWH·December 14, 2010

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·January 28, 2013

    LANCET DEVICE SNSRTR CMFRT EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 12, 2014