BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    HEARTRAK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Q-SCAN THERMOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    KA01 Chitosan Wound Dressing

    FDA 510(k)
    FDA Unclassified ·Unknown

    SPIROBAC FILTER REINF MEMBRANE

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

    CELT ACD PLUS VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·VASORUM LTD.·Product code MGB·June 11, 2025

    COLLEAGUE 3 CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 30, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 21, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014