BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TRILOGY SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER·Product code LPH·January 9, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014

    DUROM US ACETABAR COMPONENT 66/60 Z

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·December 3, 2010

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·April 8, 2021

    NEEDLE 30X1/2 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·June 29, 2021

    BD PRECISIONGLIDE¿ NEEDLES

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 13, 2023

    BD PRECISIONGLIDE¿ NEEDLES

    FDA Adverse Event
    Injury ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·May 31, 2023

    NDLE 25GA 7/8IN ECG BLT NO-ANL TRANS ORN

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·February 18, 2019

    BD PRECISIONGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·July 31, 2019