BEUDAMED
    6 results · 18ms · 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.

    TRYPTIC SOY AGAR W/10% SHEEP BLOOD

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AART CHIN IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    XMCP, HALLUX, TARSX, EXTREMITY MEDICAL SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 25, 2014

    ULTRACISION * SURG DEV, BLADES 5MM, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 6, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP·Product code MVK·August 25, 2010