BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    SENSICARE GLOVE, SIZE 8-9

    FDA Adverse Event
    BECTON DICKINSON AND CO.·Product code KGO·April 25, 1994

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·September 13, 2018

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·September 10, 2013

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 10, 2013

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·March 11, 2013

    MICROLET2 LANCING DEVICE

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE LLC·Product code NBW·February 22, 2011

    PLUM A+PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·February 19, 2008

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·July 16, 2019

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 22, 2011

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 22, 2011