BEUDAMED
    9 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARTICUL/EZE M 36MM +5

    FDA Adverse Event
    Injury ·8010379 DEPUY INTERNATIONAL·Product code JDI·February 21, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 27, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 31, 2014

    NEXGEN CRUCIATE RETAINING PEGGED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·September 13, 2017

    NEXGEN CR PEGGED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 5, 2016

    NEXGEN PRECOAT TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·March 14, 2017

    NEXGEN CR-FLEX FEMORAL COMPONENT PRECOAT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·March 14, 2017

    HERAEUS MEDICAL PALACOS R AND G BONE CEMENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·August 23, 2016

    NEXGEN LPS-FLEX FEMORAL COMPONENT SIZE G RIGHT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code NJL·April 5, 2017