BEUDAMED
    9 results · 84ms · Sources: EU EUDAMED, US FDA

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    TORQUE LIMITING DRIVER HANDLE

    FDA Adverse Event
    Injury ·TECOMET, INC.·Product code LXH·November 17, 2023

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    FDA Adverse Event
    STRYKER HOWMEDICA·Product code JWH·September 7, 2004

    LINEAGE(R) TRANSCEND(R) CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·October 2, 2013

    LINEAGE(R) TRANSCEND(R) CERAMIC ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·October 2, 2013

    TRANSCEND(R) QUADRANT SHELL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·October 2, 2013

    Stryker European Operations Limited

    Authorized representative
    🇮🇪 Ireland·16 Manufacturers

    Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.

    FDA Recall
    Terminated ·Wright Medical Technology, Inc.·Product code HRS·February 15, 2022

    PROSTEP BUNIONETTE MIS

    FDA Adverse Event
    Injury ·STRYKER CORP. / WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·April 22, 2022

    Stryker EMEA Supply Chain Services BV

    Importer
    🇳🇱 Netherlands·48 Manufacturers