BEUDAMED
    43 results · 52ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code KYF·July 12, 2022

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·October 17, 2016

    DA VINCI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·May 30, 2023

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·October 17, 2016

    DAVINCI SURGICAL SYSTEM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·November 16, 2021

    DA VINCI SP

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 7, 2022

    SMART TOUCH UNIDIRECTIONAL

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·January 14, 2026

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 17, 2019

    BALLARD MULTI-ACCESS PORT (MAP) CATHETER, DOUBLE SWIVEL Y

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code BSY·March 2, 2022

    UNK_SENSAR

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·April 1, 2022

    SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2 CORONARY IVL CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC·Product code QMG·October 15, 2025

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·July 26, 2018

    QUALA NEEDLE 30G SHORT

    FDA Adverse Event
    Injury ·SOFIC·Product code DZM·March 26, 2015

    THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 14, 2023

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code HQL·April 1, 2022

    DAVINCI SI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·April 20, 2023

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·July 26, 2018

    PULSE GEN MODEL UNKNOWN

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·July 28, 2024

    DA VINCI SURGICAL SYSTEM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·March 6, 2014

    SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAK·October 10, 2022