BEUDAMED
    60 results · 66ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SHEATHES3D

    FDA Adverse Event
    Malfunction ·SHEATHING TECHNOLOGIES, INC.·Product code ITX·August 18, 2021

    SHEATHES

    FDA Adverse Event
    Malfunction ·SHEATHING TECHNOLOGIES, INC.·Product code ITX·November 17, 2020

    MEDLINE ULTRASOUND PROBE COVER

    FDA Adverse Event
    Injury ·SHEATHING TECHNOLOGIES, INC.·Product code OIP·February 3, 2021

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·August 17, 2022

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·March 22, 2024

    WEBSTER CORONARY SINUS (CS) CATHETER WITH AUTO ID TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·June 5, 2024

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·May 27, 2025

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 4, 2019

    TEC CUTTER CATHETER

    FDA Adverse Event
    Injury ·INTERVENTIONAL TECHNOLOGIES, INC.·Product code MCW·November 4, 1999

    WEBSTER ® CS CATHETER WITH EZ STEER® THECHNOLOGY AND AUTO ID

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DRF·February 19, 2020

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·October 30, 2024

    CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DYB·August 31, 2021

    WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC.·Product code LDF·September 26, 2019

    WEBSTER ELECTROPHYSIOLOGY CATHETER WITH AUTO ID

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC.·Product code LDF·September 26, 2019

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 3, 2019

    OPTRELL MAPPING CATHETER WITH TRUEREF TECHNOLOGY

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·October 4, 2023

    CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ SMALL

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 3, 2019

    SOUNDSTAR ECO GE 8F CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC.·Product code OBJ·September 26, 2019

    SOUNDSTAR ECO GE 8F CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OBJ·October 3, 2019

    WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DRF·December 30, 2024