BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    GMK-HINGE TIBIAL AUGMENTATION SIZE 5/5MM

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

    COULTER® LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 9, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 19, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 26, 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