BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    OptoMonitor 3

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690127628·AK3 PS Insert Trial Size 6, 20mm

    PULPDENT FLUORIDE VARNISH

    FDA 510(k)
    FDA Class 2 ·Dental

    MYRIAN 1.11

    FDA 510(k)
    FDA Class 2 ·Radiology

    U-BLADE SET, TI GAMMA3 10.5X100MM

    FDA Adverse Event
    Injury ·STRYKER OSETOSYNTHESIS KIEL·Product code HSB·December 18, 2012

    BREVI-KATH RADIO-OPAQUE EPIDURAL CATHETER

    FDA Adverse Event
    Malfunction ·EPIMED·Product code BSO·November 2, 2001

    SURGICAL GUT SUTURE -PLAIN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAL·October 22, 2014

    PANORAMA

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·July 14, 2011

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 25, 2013