BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

    0.9 % Sodium Chloride Injection, USP, BD PosiFlush™ SP Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·April 6, 2026

    B-Secur HeartKey Software Library

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADAPTER CABLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code HDD·December 2, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 16, 2011

    ENDURANT AUI

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·July 29, 2013

    20 G X 1.16 IN. BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 20, 2017