BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    BOTTLE DECANTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704284942·GELPI RETRACTOR 4 1/2" SHARP POINTS

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704921062·

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209111367·KIT, TORK - CUSTOM

    TRACOE Cuff Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    THERMAGE THERMACOOL SKIN MARKETING

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

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 30, 2012

    COMPACT PORTABLE PATIENT MONITOR WITH WIRELESS ALARM

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·September 27, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015