BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 29, 2010

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 11, 2013

    ENDOTAK C

    FDA Adverse Event
    Injury ·HISTORICAL CPI ST. PAUL·Product code LWS·July 3, 2014

    MLRY-HD POR FMRL 12X165MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 1, 2018

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 1, 2018

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LQM·June 21, 2018

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LQM·June 21, 2018

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LQM·June 22, 2018

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 1, 2018

    M2A-MAGNUM 42-50MM TPR INSRT-6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 1, 2018