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

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    THE DENVER SPLINT

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ORTHO H FILM

    FDA 510(k)
    FDA Class 1 ·Radiology

    FINESS SINUS TREATMENT SYSTEM (ACCESS SHEATH COMPONENT)

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014

    CARELINK PROGRAM W/TELEMETRY C

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·October 15, 2012

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL CO·Product code OAD·August 4, 2010