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

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    PureLift Pro Plus

    FDA 510(k)
    FDA Class 2 ·Neurology

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·March 13, 2023

    56 SERIES JET NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    JOURNEY II CR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DRILL, AO T2 FEMUR 4,2X340 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 27, 2020

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2025

    CELL-DYN 1700 CS ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 7, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 17, 2011

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 11, 2013