BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    SILICONE PUNCTAL PLUG

    FDA 510(k)
    FDA Unclassified ·Unknown

    Hexanium® TLIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF

    FDA 510(k)
    FDA Class 2 ·Neurology

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 30, 2013

    XCEL DILATING TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·February 7, 2011

    UNKNOWN NEUROMODULATION STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·August 5, 2014