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

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    EXTERNAL PULSE GENERATOR FOR TEMP. STIM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BARRIER-PRO CO-POLYMER PATIENT EXAMINATION GLOVE, POWDERED, WHITE (NON-COLORED) OR GREEN COLORED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CONTAIN X-RAY DETECTABLE LAP SPONGE

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

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 27, 2014

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 14, 2012

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 MEDIUM-LARGE TITANIUM LIGA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code FZP·January 15, 2008