BEUDAMED
    13 results · 46ms · Sources: EU EUDAMED, US FDA

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    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 28, 2003

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·September 18, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 21, 2025

    TRUSTEEL

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

    STYLE 168 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·June 9, 2021

    ENDOTAK

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC.·Product code LWS·August 29, 1997

    ARROW/KONTRON 8FR INTRA-AORTIC BALLOON

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·February 20, 2001

    CIDEX ACTIVATED DIALDEHYDE SOLUTION

    FDA Adverse Event
    Injury ·ADVANCED STERILIZATION PRODUCTS·Product code LRJ·March 30, 1999

    LENSX LASER SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON LENSX, INC.·Product code OOE·September 17, 2019

    INSET 30

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·November 21, 2025

    OPEN PIVOT AP MITRAL HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWQ·April 4, 2023

    LAUNCHER UNK GUIDE CATHETER

    FDA Adverse Event
    Death ·MEDTRONIC, INC·Product code DQY·May 9, 2025

    MOSAIC MITRAL BIOPROSTHETIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·April 4, 2023