BEUDAMED
    6 results · 20ms · 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 ×

    NERIA GUARD

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·September 24, 2025

    INTERMEDIARY TUBESET 24PK

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HRX·May 31, 2022

    REVERSE SHOULDER SYSTEM GLENOID BASEPLATE 27X15

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·March 12, 2021

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLQ·March 11, 2013

    COULTER AC*T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 27, 2011

    OT ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·February 21, 2008