BEUDAMED
    6 results · 23ms · 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.

    MEPITEL NON-ADHERENT SILICONE DRESSING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    REDI-RELEASE ABSORBENT DRESSING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CRANIAL-SCR PLUSDRIVE Ø1.6 SELF-DRILL L4

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code JEY·January 14, 2013

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·December 3, 2010

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 3, 2014