BEUDAMED
    8 results · 35ms · Sources: EU EUDAMED, US FDA

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    WIRE DRIVER & FIXATION DRILL

    FDA Adverse Event
    Malfunction ·LINVATEC CORP.·Product code HTW·December 22, 2005

    DELTA CERAMIC FEM HD 36/-3MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·July 31, 2017

    TPRLC 133 FP TYPE1 BM SO 10.0

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 31, 2017

    G7 BONEMASTER LTD ACET SHL 52E

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 31, 2017

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 25, 2013

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·March 9, 2011

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·March 27, 2008

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015