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

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    UTAH CVX-RIPE

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814275·GENUMEDI PT SILVER R IV

    T PLATE

    FDA UDI
    Biomet Orthopedics, LLC·00887868004377·

    Prime Medical LLC

    FDA UDI
    Prime Medical LLC·00850055249288·PrimePadPlus-K14-3422

    BD BBL¿ COLUMBIA AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code KZI·July 10, 2023

    SAFIRE

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOFRIC SINGLE USE URINARY CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACCU-CHEK ® ACCUTREND TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CGA·June 3, 2013

    VIRTUOSO II DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 29, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008