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

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    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    2520274-2013-01319

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·March 6, 2013

    O-F 4000 PLUS

    FDA Adverse Event
    Injury ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 10, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    UNKNOWN OPSITE FLEXIGRID

    FDA Adverse Event
    Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·January 8, 2023

    BACTIGRAS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code FRO·January 8, 2023

    INFLATOR KIT 18INFKIT BALLOON

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRC·August 15, 2014