BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    SIGNET DXIS DIRECT X-RAY IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    PROCARE

    FDA UDI
    DJO, LLC·00888912009669·TRANSITIONAL 172 COLLAR, ADULT SHORT

    DISPOSABLE AMNIOTOME

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARGENCO IV

    FDA 510(k)
    FDA Class 2 ·Dental

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NPT·February 16, 2024

    HYPODERMIC NEEDLE-PRO AND NEEDLE WITH NEEDLE PROTECTION DEVICE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMJ·February 4, 2013

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON MANUFACTURING, LTD.·Product code HQC·July 2, 2014

    Exactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 38, 41, 44 head, Large, Item Number 314-13-04; Shoulder Arthroplasty

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