BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 12, 2014

    DRUG-ELUTING PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·February 11, 2013

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·January 10, 2011