BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    TIBIAL ARTICULAR SURFACE PROVISIONAL RIGHT SIZE GH

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·June 5, 2018

    PS TIBIAL ARTICULAR SURFACE PROVISIONAL RIGHT SIZE 10-12 GH TOP

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·June 5, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL RIGHT SIZE GH

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·June 5, 2018

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·April 2, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 9, 2011

    POLYFLUX LR CAPILLARY DIALYZER

    FDA Adverse Event
    Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code MSF·April 16, 2008

    PS TIBIAL ARTICULAR SURFACE PROVISIONAL RIGHT SIZE 10-12 GH TOP

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·June 5, 2018

    BASE SYSTEM, ILLUMENA

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM·Product code DXT·September 16, 2025