BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    K-ASSAY MYOGLOBIN ASSAY, K-ASSAY MYOGLOBIN CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Immunology

    SINGLE USE VINYL EXAM GLOVES - COLOR CODED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC

    FDA 510(k)
    FDA Class 2 ·Neurology

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    RENEW RECEIVER KIT, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 4, 2015

    ASR ACETABULAR IMPLANT 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 7, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 8, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014