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

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    Filters FDA Adverse Event ×

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 2, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 21, 2012

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·September 15, 2010

    COMPR NANO HMRL PPS 32MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·September 11, 2019

    PT HYBRID GLEN POST REGENEREX GENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·August 1, 2019

    MODULAR HYBRID GLENOID POST¿REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 16, 2018

    MODULAR HYBRID GLENOID BASE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 16, 2018

    COMPREHENSIVE STANDARD TAPER ADAPTOR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·November 16, 2018

    PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 31, 2019

    COMPREHENSIVE STANDARD TAPER ADAPTOR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·May 31, 2019

    SM HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 31, 2019