BEUDAMED
    8 results · 73ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SYNVISC ONE

    FDA Adverse Event
    GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·November 22, 2013

    TAPERLOC POR FMRL LAT 13.5X147

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 21, 2014

    M2A-38 CUP NON FLARED SZ 58MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 21, 2014

    M2A 38MM MOD HD -3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 19, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 8, 2016

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME CORPORATION·Product code MOZ·May 3, 2022

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·April 3, 2019

    TRIATHLON LEFT KNEE REPLACEMENT

    FDA Adverse Event
    Injury ·STRYKER(SUZHOU) MEDICAL TECHNOLOGY CO.,LTD.·Product code JWH·November 23, 2021