BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    GMK-HINGE TIBIAL AUGMENTATION SIZE 5/5MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KRO·August 31, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 30, 2025

    V SERIES MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·May 1, 2013

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 28, 2014

    GMK-REVISION TIBIAL WEDGE SIZE 4/10MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2016

    ACTIVA

    FDA Adverse Event
    Malfunction ·MPRI·Product code MHY·September 24, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·MPRI·Product code MHY·September 24, 2020

    GMK-REVISION TIBIAL AUGMENTATION SIZE 3/10MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KRO·July 19, 2017

    GMK-REVISION OFFSET ADAPTER 5 MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·February 8, 2017

    GMK REVISION OFFSET ADAPTER 5MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·February 16, 2018