BEUDAMED
    3 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·June 23, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 2, 2013

    HBO VENT, MODEL HV-500A

    FDA Adverse Event
    Malfunction ·SECHRIST INDUSTRIES, INC.·Product code CBK·December 3, 2010