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 ×

    3D DENTAL DIAMOND ROTARY INSTRUMENTS

    FDA 510(k)
    FDA Class 1 ·Dental

    HORIZON ECG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMITH & NEPHEW TWINFIX ULTRA HA SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M2A MAGNUM MODULAR HD COCR 42MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 25, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 2, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 1, 2010