BEUDAMED
    7 results · 31ms · 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.
    Filters FDA Adverse Event ×

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS &CABLE SLEEV

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 30, 2016

    IMP CBL DIA2 SS & CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·July 20, 2016

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·February 25, 2013

    VENTRIO MESH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·January 25, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014