BEUDAMED
    8 results · 20ms · 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 ×

    DUPONT SALICYLATE CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Hex Screwdriver

    FDA UDI
    Biomet Orthopedics, LLC·00887868567520·

    HEX SCREWDRIVER

    FDA UDI
    Biomet Orthopedics, LLC·00880304405523·

    PASSAGE AIRWAY SPLINT

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    KARE CHAIR I

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ACCESSORY DRAIN BAG

    FDA Adverse Event
    Malfunction ·GAMBRO·Product code KDI·November 14, 2010

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 4, 2012