BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GALAXY G3 MINI 1MM X 1CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 13, 2020

    BAXANO IO-FLEX SYSTEM

    FDA Adverse Event
    Other ·BAXANO, INC.·Product code HAE·July 2, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·May 1, 2013

    STREAMLINE MIS PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·PIONEER SURGICAL·Product code NKB·August 28, 2014

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·May 20, 2011

    BAXANO IO-FLEX SYSTEM

    FDA Adverse Event
    Other ·BAXANO, INC.·Product code HAE·July 2, 2012

    UNKNOWN NEXGEN FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 8, 2022

    UNKNOWN FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 8, 2022

    UNKNOWN ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 8, 2022

    UNKNOWN NEXGEN LPS-FLEX PS TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 8, 2022

    UNKNOWN NEXGEN LPS-FLEX PS TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 8, 2022