BEUDAMED
    14 results · 53ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    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

    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

    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

    SINGLE USE ELECTROSURGICAL KNIFE

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

    ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIU·June 18, 2019

    COBAS AMPLIPREP INSTRUMENT

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS LTD.·Product code JJH·September 5, 2013

    COBAS AMPLIPREP INSTRUMENT

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS LTD.·Product code JJH·September 5, 2013

    RAPIDLAB 1245 BLOOD GAS SYSTEM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS, LTD·Product code CHL·April 18, 2008