BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    ILLUMINATOR III

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR

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

    TMD SAFETY SYRINGE (FA12 SERIES 3ML/FA13 SERIES 5ML)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    19CM STRAIGHT HEMOSPLIT MI KIT WITH AIRGUARD

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD)·Product code MSD·January 11, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·February 5, 2014

    REVEAL DX

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·December 13, 2010

    PAIN MANAGEMENT PORTEX EPIDURAL CONTINUOUS TRAYS

    FDA Adverse Event
    Injury ·Product code CAZ·July 13, 2020