BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    CRITIKON OXYGEN MONITOR, MODEL 8030

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    STRADIS HEALTHCARE

    FDA UDI
    STRADIS MEDICAL, LLC·M75268219360·

    MOIST PUNCTAL PLUG SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    NAVIOPFS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 20, 2014

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 7, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 5, 2015

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024