BEUDAMED
    6 results · 23ms · 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.

    HEEL OR ELBOW PROTECTOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Velofix™ TLIF Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVANTIV SAFETY I.V. CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNKNOWN DEPUY ASR ADAPTER SLEEVE

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 4, 2012

    KNIFE

    FDA Adverse Event
    Malfunction ·ALCON MANUFACTURING, LTD.·Product code HNN·December 18, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NPZ·July 23, 2010