BEUDAMED
    10 results · 22ms · 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 ×

    I PORT ADVANCE

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 26, 2024

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·May 2, 2019

    AMPLATZER VASCULAR PLUG 4

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code KRD·July 15, 2015

    I-PORT ADVANCE

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FOZ·August 9, 2024

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·May 9, 2019

    PDS LL PLUS ANTIBACTERIAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code NEW·March 14, 2013

    AIR OPTIX NIGHT & DAY AQUA

    FDA Adverse Event
    Injury ·PT CIBA VISION BATAM·Product code LPM·February 24, 2011

    HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code LFL·February 8, 2008

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·May 2, 2019

    UNSPECIFIED BD ECLIPSE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMF·May 2, 2019