BEUDAMED
    7 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.

    KENDALL TRU-CLOSE INFECTION CONTROL EVACUATOR

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

    FDP - SLIDEX DIRECT

    FDA 510(k)
    FDA Class 2 ·Hematology

    SURGICAL INSTRUMENT KIT, DISPOSABLE

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

    EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·July 18, 2018

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 23, 2013

    MAXIMO II VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014