BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    FIBEROPTIC LARYNGOSCOPE HANDLE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    VIASPAN

    FDA Adverse Event
    Other ·FRESENIUS KABI AUSTRIA GMBH·Product code KDL·March 26, 2012

    OPHTHASCAN B

    FDA 510(k)
    FDA Class 2 ·Radiology

    THERMO-FLOW SET

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·June 2, 2006

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·June 2, 2006

    MONARCH IOL DELIVERY SYSTEM CARTRIDGE

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code KYB·June 2, 2006

    APC PLUS, CLARITY, MINI UNI-TWIN, VICTORY SERIES

    FDA Adverse Event
    Injury ·3M UNITEK·Product code DYH·May 9, 2012

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 5, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 18, 2014

    DEXTRUS

    FDA Adverse Event
    Injury ·EXTERNAL MANUFACTURER·Product code NVN·January 3, 2011