BEUDAMED
    19 results · 39ms · Sources: EU EUDAMED, US FDA

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    BD Pen Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD NANO¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 4, 2019

    BD NANO¿ 2ND GEN PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 7, 2022

    BD ULTRA FINE PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 11, 2020

    PEN NDL 32G 4MM 5B XTW BULK US W/EXPIRY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 13, 2020

    BD ULTRA-FINE¿ MINI PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·February 5, 2019

    BD¿ ULTRA-FINE PEN NEEDLES

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·January 24, 2019

    RELION PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FMI·March 25, 2021

    BD ULTRA FINE¿ SHORT INSULIN PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 27, 2018

    6MM X 32G PEN NEEDLE (ULTRAFINE MICRO)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 11, 2021

    BD ULTRA FINE¿ PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 18, 2019

    31G PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·April 17, 2009

    LUCINA MODEL MELODI

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ACCESS THYROGLOBULIN ANTIBODY II ASSAY, MODELS A32898 (REAGENT) AND A36920 (CALIBRATORS)

    FDA 510(k)
    FDA Class 2 ·Immunology

    SCRDRIVER W/T-HANDLE STD F/MATRIX 5.5

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·June 11, 2013

    SELUTE PICOTIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 14, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 21, 2017

    ECHELON 60

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 11, 2019