BEUDAMED
    199 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·May 27, 2021

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Injury ·ALCON·Product code HQC·March 19, 2012

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·April 24, 2017

    EVIS X1 VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·January 17, 2025

    UNK

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·January 31, 2019

    LIBERTY SELECT CYCLER ASSY(NON-VALUATED)

    FDA Adverse Event
    Injury ·CONCORD MANUFACTURING·Product code FKX·February 6, 2020

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·October 6, 2021

    GENESIS

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW RICHARDS·Product code HSX·April 27, 1993

    ENTERRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·July 1, 2013

    GYNECARE TVT OBTURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·August 9, 2013

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·January 22, 2015

    SURGICEL POWDER USA - ABSORBABLE HEMOSTATIC PWDR

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code LMG·June 18, 2021

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND, (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·July 22, 2009

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 3, 2015

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    CAPSULE DEPLOYMENT DEVICE

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION / UNITED STATES ENDOSCOPY GROUP·Product code NEZ·November 25, 2024

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code MUZ·January 9, 2015

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·April 11, 2018

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·November 25, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·May 6, 2015