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

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    Filters FDA Adverse Event ×

    MEDACTA KNEE IMPLANTS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 28, 2016

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·August 4, 2015

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·July 28, 2015

    PERMACOL 15X20 1.5MM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES·Product code FTL·April 24, 2013

    UNKNOWN_CORK_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·September 16, 2014

    MICRUS MICROCOIL SYSTEM

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR CORPORATION·Product code MJN·April 19, 2011

    C8701, S ALEXIS LAP SYS W/ KII FIOS 5/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·November 14, 2016