BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 18, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 18, 2010

    EON PATIENT PROGRAMMER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 17, 2012

    BIOMET FIXED CRUCIATE TIBIAL PLATE WITH LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2019

    BIOMET FIXED CRUCIATE TIBIAL PLATE WITH LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2019

    BIOMET (R) INTERLOK FIXED CRUCIATE TIBIAL PLATE WITH LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2019

    VANGUARD (TM) PS OPEN BOX FEMORAL RIGHT INTERLOK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·April 23, 2019

    VANGUARD (TM) E-POLY (TM) PS TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·April 23, 2019

    VANGUARD (TM) E-POLY (TM) PS TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·April 23, 2019

    BIOMET ARCOM ALL POLY PAT. BUTTON

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2019

    BIOMET (R) INTERLOK FIXED CRUCIATE TIBIAL PLATE WITH LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 23, 2019