117 results · 53ms · Sources: EU EUDAMED, US FDA

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Median Technologies

Manufacturer
🇫🇷 France

LMS-Lung/TRACK

FDA UDI
MEDIAN TECHNOLOGIES·03760263520017·LMS-Lung/TRACK is intended to provide the radio...

LMS-Liver

FDA UDI
MEDIAN TECHNOLOGIES·03760263520024·LMS-Liver is an image analysis software applica...

ACCUTITE

FDA Adverse Event
Injury ·INMODE LTD.·Product code GEI·April 29, 2025

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·January 31, 2024

TALENT TAA

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 19, 2014

MAZOR X SYSTEM

FDA Adverse Event
Malfunction ·MAZOR ROBOTICS LTD·Product code OLO·May 30, 2025

PIPELINE

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 11, 2024

PIPELINE FLEX W/SHIELD TECHNOLOGY

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·October 11, 2024

VISUALASE SYSTEM

FDA Adverse Event
Death ·MEDTRONIC NAVIGATION, INC·Product code GEX·September 3, 2024

HEARTMATE 3 LVAS IMPLANT KIT

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·June 15, 2022

ALTO

FDA Adverse Event
Malfunction ·ENDOLOGIX SANTA ROSA·Product code MIH·April 20, 2026

ALTO

FDA Adverse Event
Injury ·ENDOLOGIX SANTA ROSA·Product code MIH·April 20, 2026

SURGICEL ABSORBABLE HEMOSTAT UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code LMG·October 26, 2021

ON-X PROSTHETIC AORTIC VALVE UNKNOWN CONFIGURATION

FDA Adverse Event
Death ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·June 14, 2019

NEU_INTERSTIM_INS

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·March 28, 2017

EMBLEM S-ICD

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·April 17, 2023

EMBLEM S-ICD

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·April 17, 2023

MELODY TRANSCATHETER PULMONARY VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·November 12, 2021

STRUCTURAL HEART PRODUCT

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 12, 2015