BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    4MP COLOR LCD MONITOR, RADIFORCERX430

    FDA 510(k)
    FDA Class 2 ·Radiology

    TLIF/PLIF Disc Prep

    FDA UDI
    Life Spine, Inc.·00190837087050·

    FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR

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

    BIS/EEG MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 16, 2026

    ACCU-CHEK ® SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 14, 2013

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·April 28, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    DEKA SMARTXIDE² TRIO

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 31, 2023

    BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021