BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    NASAL ONE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111223723·GUYON SOUND W/THREAD 28FR

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209110162·

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 8, 2020

    CASSIE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Pulse H20h!

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

    EASYTRAK 2

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·October 4, 2010

    MULTI-LUMEN/PSI KIT

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FOZ·November 14, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

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