BEUDAMED
    11 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    G7 54-F PPS LIMITED ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·October 2, 2017

    DELTA CER FEM HD 32/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 19, 2017

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 18, 2024

    ECHO BI-METRIC 13MMX145MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 2, 2017

    DELTA CER FEM HD 32/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 5, 2017

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 2, 2024

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 5, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·October 15, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·August 4, 2010

    ECHO POR FMRL NC 13X145MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 16, 2017

    DELTA CER FEM HD 32/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 5, 2017