BEUDAMED
    164 results · 71ms · Sources: EU EUDAMED, US FDA

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    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR CHILDREN

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·February 8, 2002

    BD RAPID DETECTION OF SARS-COV-2 VERITOR ASSAY

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·October 27, 2020

    BD PEN NEEDLE 32GX4MM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FMI·December 17, 2020

    EVIS LUCERA ELITE DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·December 12, 2023

    BIOPSY FORCEPS

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FCL·December 12, 2023

    SINGLE USE 3-LUMEN SPHINCTEROTOME V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·December 12, 2023

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·December 11, 2023

    EVIS DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·December 12, 2023

    BD¿ STEM CELL ENUMERATION

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·December 12, 2023

    BD MULTITEST¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·October 8, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 24, 2022

    UNKNOWN PROGRIP MESH PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 24, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 1, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 24, 2022

    EVIS LUCERA ELITE COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·December 18, 2023

    HEARTSINE SAMARITAN 300P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·May 21, 2019

    FEMORAL STEM 12/14 NECK TAPER PRESS-FIT CEMENTLESS SIZE 10 STANDARD OFFSET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 4, 2024

    EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - PARTIALLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code ESW·January 3, 2019

    LETSGETCHECKED BLOOD SAMPLE COLLECTION KIT

    FDA Adverse Event
    Malfunction ·PRIVAPATH DIAGNOSTICS LTD·Product code PQD·May 6, 2026

    SINGLE USE ELECTROSURGICAL KNIFE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·February 23, 2022