BEUDAMED
    6 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    REVOLUTION PHISIO CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code KFM·May 20, 2021

    REVOLUTION CENTRIFUGAL BLOOD PUMP

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code KFM·March 19, 2022

    LOCKING SCREW, FULLY THREADED 5X55 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020