BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    VES 1501-M

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Fresh Cells

    FDA UDI
    DIAGNOSTIC HYBRIDS, INC.·30014613335283·H&V-MIX MWP W24/09F

    SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Applied Tissue Technologies PWD™ Platform Wound Dressing

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY

    FDA Adverse Event
    Injury ·Product code DTZ·September 11, 2007

    3.5MM/2.7MM T-PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA) ELMIRA·Product code HRS·February 26, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 9, 2011

    HUMERAL NAIL, AP T2 HUMERUS Ø7X240 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·August 6, 2014