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

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    STIMU-TAP

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704266993·

    Calibration Solution

    FDA UDI
    Radiometer Medical ApS·05700699440242·S1720 Calibration Solution 1 200 mL, for ABL7XX

    Solstice Occipito-Cervico-Thoracic System

    FDA UDI
    Life Spine, Inc.·00190837024895·SOLSTICE Polyaxial Screw Assembly 4.0mm x 24mm

    CREATININE REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CEMPER

    FDA 510(k)
    FDA Class 2 ·Dental

    SPIROBAC FILTER REINF MEMBRANE

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code CAH·August 1, 2012

    IAB: 8 FR - 40 CC

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DSP·December 3, 2010

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 5, 2013

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 18, 2014

    ABL7XX Calibration 1 Solution S1720. P/N S1720, 944-024 Intended for in vitro testing of samples of whole blood for the parameters pH, pO2, pCO2, potassium, sodium, calcium, chloride, glucose, lactate, total bilirubin, and co-oximetry parameters (total hemoglobin, oxygen saturation, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb, FHbF). Also, intended for in vitro testing of samples of expired air for the parameters pO2 and pCO2.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code JFP·September 5, 2008