BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    TI-CORE NEW & IMPROVED

    FDA 510(k)
    FDA Class 2 ·Dental

    STERNGOLD 1, MODEL 1127781

    FDA 510(k)
    FDA Class 2 ·Dental

    SPACE CHAMBER PLUS COMPACT SPACE CHAMBER PLUS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·April 4, 2014

    THERMAL SENSORY ANALYZER (TSA-II)

    FDA Adverse Event
    Injury ·MEDOC LTD., ADVANCED MEDICAL SURGERY MEDISCENSE USA·Product code LQW·December 26, 2019

    DUROM HIP GENERIC

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWY·January 15, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·February 5, 2014

    KAPPA 400 DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·December 13, 2010

    QSENSE CPM THERMAL SENSORY ANALYZER 2001

    FDA Adverse Event
    Malfunction ·MEDOC LTD, ADVANCED MEDICAL SYSTEM·Product code LQW·April 19, 2022