BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    3M TEGADERM HP TRANSPARENT DRESSING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BARCO

    FDA UDI
    Barco NV·05415334042414·MDSC-8532 NXF

    PALS PLATINUM NEUROSTIMULATION ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    EUSOL-C

    FDA 510(k)
    FDA Unclassified ·Unknown

    NEURO DIAMOND DRILL, MEDIUM

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code HBE·January 24, 2013

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 17, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 14, 2014

    SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·April 20, 2016