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

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    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515019416·Heiss Artery Fcps, del, 90 deg jaws, 9 1/2"

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857581364·Split Tube Retractor Ø22x30 mm

    UNIMAX VERESS NEEDLE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SAS INFLUENZA A TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2013

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011