BEUDAMED
    5 results · 15ms · 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 Status: Malfunction ×

    BD ULTRA FINE¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMI·January 29, 2019

    BD ULTRA FINE¿ PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMI·December 17, 2018

    G7 POSITIONING GUIDE ROD

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LXH·November 13, 2024

    NAVIGATION SYSTEM II - CART

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HAW·April 23, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008