BEUDAMED
    6 results · 16ms · 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.

    INSTRUMENT TRAY

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ACUSON P50 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Dynarex Three-Way Stopcock

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAPIOX FX OXYGENATOR W/O RESERVOIR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 2, 2012

    CUSTOM PAK

    FDA Adverse Event
    Malfunction ·ALCON - HOUSTON·Product code KYG·December 19, 2013

    UNK DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·July 22, 2010