BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 13, 2013

    GENESISXP IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 27, 2011

    ICY CATHETER

    FDA Adverse Event
    Death ·ALSIUS CORP.·Product code DQO·April 22, 2008

    BIOMET SPLINED KNEE STEM V2

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBV·August 4, 2020

    BIOMET SPLINED KNEE STEM V2

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBV·August 4, 2020

    BIOMET 360 TIBIAL AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 4, 2020

    VANGUARD 360 DISTAL FEMORAL AUGMENT LL/RM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 4, 2020

    BIOMET 360 TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 4, 2020