BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RHEAD RECON STEM IMPLANT NON-COATED, SIZE 4

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code KWI·December 29, 2015

    ATTUNE PS FEM LT SZ 6 CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·May 26, 2020

    ATTUNE PS FEM LT SZ 4 NAR CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·November 16, 2020

    POSEY BED

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code OYS·April 26, 2013

    GENERATOR, VULCAN CE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GEI·September 18, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 23, 2011

    ATTUNE PS FEM RT SZ 9 CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·June 1, 2020

    AZURE XT DR MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NVZ·January 18, 2023