BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    ULTRACHECK CURVE BLOOD PRESSURE CUFFS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 36cm x 130°

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665023473·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970508·

    MICROPLEX COIL SYSTEM- COSMOS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STRYKER NAVIGATION SYSTEM - HIP MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

    TI PANGEA(TM) LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·May 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 13, 2011

    ADVIA CHEMISTRY CALCIUM_2 METHOD

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS, INC.·Product code CJY·August 14, 2008

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 6, 2014

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 6, 2014

    UNITIP CATHETER FOR HR GI

    FDA Adverse Event
    Malfunction ·UNISENSOR USA INC·Product code FFX·January 16, 2015