BEUDAMED
    5 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·January 31, 2019

    CONSTRAINED LINER WITH CONSTRAINING RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·January 31, 2019

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    AED PLUS

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 18, 2014