BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    KOGENT SPETZLER LIGHTED SUCTION TUBES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304232914·

    GYMFORM DUAL FLEX BELT MODEL WB-162

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VENTILAIR II MEDICAL AIR COMPRESSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CLEARVIEW UTERINE MANIPULATOR

    FDA Adverse Event
    Injury ·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024

    UNSPECIFIED PRIMARY PLUM SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·October 3, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    OT PENLET PLUS

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·June 27, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    UNSPECIFIED PRIMARY PLUM SET CLAVE PORT, CLAVE Y-SITE, SECURE LOCK

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·November 24, 2024