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

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    CRI CYNOSAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EZLOC

    FDA UDI
    Biomet Sports Medicine, LLC·00880304457348·

    9 - 10 MM EZLOC FEMORAL FIXATION LONG

    FDA Adverse Event
    Injury ·BIOMET SPORTS MEDICINE·Product code MBI·May 20, 2009

    NEWPORT WAVE VENTILATOR MODEL E200

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MICRO 2 SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 22, 2010

    2124215-2014-12092

    FDA Adverse Event
    Malfunction ·GUIDANT PUERTO RICO BV·Product code NVZ·July 1, 2014

    ACUITY CENTRAL MONITORING

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·December 5, 2012

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026