BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    FCI CRAWFORD PROBE INTUBATION SETS

    FDA 510(k)
    FDA Unclassified ·Unknown

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517403056·CoRoent XLR-F, 12x38x32 12° Gamma

    Monolith

    FDA UDI
    Nuvasive, Inc.·00887517697899·Monolith Core, Ø12x38mm

    Pro-Retractor Malleable Blade

    FDA UDI
    KOROS U.S.A., INC.·10840199542571·Pro-Retractor Deep Malleable Blade Large 3 x 8"

    UNI-VENT-731 SERIES VENTILATORS, MODEL 731EMV+

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Zimmer Guide Wire Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZEPHIR ANTERIOR CERVICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·February 15, 2011

    SIGMA 100 S

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code NVZ·August 8, 2014