BEUDAMED
    12 results · 19ms · 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 ×

    MEDICA IIF-MULTIPLE ANTIBODY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    EasyTouch

    FDA UDI
    MHC MEDICAL PRODUCTS, LLC·MHC18311001·

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690114895·Femoral Augment Posterior, Size 1, 10mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690123637·Femoral Posterior Augment Trial Size 1, 10mm

    LONESTAR

    FDA UDI
    Orthofix US LLC·18257200124008·LONESTAR - RASP CASE

    T7Plus

    FDA UDI
    STRYKER CORPORATION·07613327466102·Zippered Toga with Peel Away

    Steri-Shield

    FDA UDI
    STRYKER CORPORATION·07613327625301·8 Zippered Toga with Peel Away Face Shield

    STREAMLINE TL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES VENTROFIX MIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·May 23, 2014

    UNKNOWN RIGHT REJUVENATE HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 2, 2012

    PROMOTE PLUS CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 10, 2010