BEUDAMED
    10 results · 27ms · 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 ×

    MCINTOSH, MILLER, FOREGGER BABY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ORTHOFIX MODULSYSTEM

    FDA UDI
    ORTHOFIX SRL·18053800895726·SELFDRILLING XCALIBER CYLINDRICAL SCREW SS L150...

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105740·SCISSORS HORIZONTAL CURVED 25GA

    Guided Inserter

    FDA UDI
    BICON, LLC·00813110026477·4.5mm Guided Inserter - 2.5mm Post

    ORTHOFIX MODULSYSTEM

    FDA UDI
    ORTHOFIX SRL·18053800895535·SELFDRILLING XCALIBER CYLINDRICAL SCREW SS L150...

    SPECIFIC IGE EIA-TURBO ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    SPORVIEW

    FDA 510(k)
    FDA Class 2 ·General Hospital

    QUADROX-ID PEDIATRIC

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 1, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 30, 2010

    ZOLL IVTM SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code NCX·July 21, 2014