BEUDAMED
    320 results · 28ms · Sources: EU EUDAMED, US FDA

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    BODYCAP

    FDA registration
    BODYCAP·1 product·🇫🇷 France

    e-Viewer Medical monitor

    FDA UDI
    BODYCAP·03665810000038·

    Activator Medical

    FDA UDI
    BODYCAP·03665810000045·

    e-Celsius Medical pill

    FDA UDI
    BODYCAP·03665810000168·

    e-Celsius Medical System

    FDA UDI
    BODYCAP·03665810000083·

    ARROW PSI SET: 9 FR

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code DYB·August 11, 2025

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 6, 2009

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 19, 2010

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 16, 2009

    ENDO SMARTCAP

    FDA Adverse Event
    Malfunction ·MEDIVATORS INC.·Product code FAJ·October 11, 2024

    SPRINT QUATTRO SECURE MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO VILLALBA·Product code NVY·April 23, 2026

    VALVE SET, EM2400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·August 7, 2020

    LINOX S 65

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·January 9, 2017

    ULTRASONIC GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·September 2, 2022

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·March 14, 2017

    LANTERN DELIVERY CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·September 13, 2019

    CLAVE CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL INC.·Product code FPA·January 10, 2013

    SURESTEP FOLEY TRAY - BARDEX I.C. WITH HYDROGEL AND BACTI-GUARD SILVER ALLOY, 14

    FDA Adverse Event
    Injury ·PRODUCTOS PARA EL CUIDADO DE LA SALUD -9611590·Product code MJC·October 19, 2016

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Death ·COOK, INC.·Product code MIH·November 12, 2010

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·December 16, 2020