BEUDAMED
    8 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

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 9, 2013

    PENUMBRA SYSTEM SEPARATOR FLEX 032

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·April 12, 2011

    GMK-REVISION TIBIAL WEDGE SIZE 4/10MM

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

    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

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024