BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/12MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 26, 2016

    GMK-REVISION FEMUR REVISION PS SIZE 4 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 27, 2019

    TRANSSEPTAL NEEDLE, BRK 1, 71CM

    FDA Adverse Event
    Other ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·July 2, 2009

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 21, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 26, 2014

    SCREW-IN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 13, 2011

    PLATE ADAPTER DIST. LAT. FEMUR RIGHT

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HWC·May 11, 2017