BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    BARD UMBILICAL VESSEL CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FlexCare 8906-85 200*85*13cm

    Device
    EU MDR · Eu Md Class 1 ·Vevia Finland Oy·On the market

    POSI-TOT

    FDA 510(k)
    FDA Class 2 ·Radiology

    Hair Growth System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UNIFY ASSURA CRT-D

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NIK·January 13, 2014

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DRY·November 1, 2010

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·December 21, 2012