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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    NEEDLE 27X1/2 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·November 25, 2020

    BD PRECISIONGLIDE¿ NEEDLEZ

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 9, 2019

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OYC·December 9, 2019

    BD PRECISIONGLIDE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·April 8, 2023

    ARCHITECT AFP

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND·Product code LOK·November 14, 2014

    ASR ACETABULAR IMPLANT 56

    FDA Adverse Event
    Injury ·DEPUY WARSAW·Product code KWA·September 16, 2011

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·July 26, 2013