BEUDAMED
    8 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NIO ADULT

    FDA Adverse Event
    Malfunction ·WAISMED LTD·Product code FMI·July 24, 2023

    3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 11.5MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·October 3, 2019

    3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 3.25 X 11.5MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·July 10, 2019

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·April 1, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·March 9, 2011

    ONYX, ANEURYSM

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code MFE·May 7, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 7, 2016

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·January 9, 2025