BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    6.2 VITALLIUM ALLOY CANCELLOUS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STIMTECH SD PATIENT 6089 #78-8050

    FDA 510(k)
    FDA Class 2 ·Neurology

    ECLIPSE 2100(TM), MODIFICATION

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

    FORCEPS CEV134 BIPOLAR 350MM MOUIEL

    FDA Adverse Event
    Malfunction ·INTEGRA MICROFRANCE S.A.S.·Product code GEI·October 23, 2019

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013

    SYMB SET2YSITES W/FI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 6, 2010

    LIGAMAX 5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 18, 2014