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

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    Zimmer Guide Wire Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

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

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AFFIX SPINOUS PROCESS PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 19, 2011

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 26, 2013

    GOLD PROBE HEMOSTASIS CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 25, 2008