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

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    ChoICE Guide Wire, Mailman Guide Wire, Luge Guide Wire, ChoICE PT Guide Wire, PT Graphix Wire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013402392·MARKS NEEDLE, #19

    SUCRALFATE AND CARAFATE PASTE KITS

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE BLLOD COLLECTION NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·September 10, 2024

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND·Product code FMI·January 8, 2024

    BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·January 25, 2019

    PEN NDL 32G 4MM 100BX 1200 USA

    FDA Adverse Event
    Malfunction ·BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND·Product code FMI·March 1, 2024

    OXINIUM PRIMARY 40MM MODULAR HEAD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·October 6, 2014

    COULTER AC*T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 3, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 29, 2011

    PN 31X8 100 PK GERMANY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·June 5, 2019