BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    HEMOGLOBIN REAGENT

    FDA 510(k)
    FDA Class 2 ·Hematology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909107452·REVELATION DIAMOND 859-010C - 5 PACK

    EMS 3000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HELICOBACTER PYLORI ELISA IGG TEST KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PERITONEAL CATHETER WITH BIOGLIDE, 8 SLITS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·November 23, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 2, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 4, 2012

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·July 15, 2013

    ASPHERE M SPEC 12/14 40 +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·July 15, 2013

    OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·June 26, 2024