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GIE MEDICAL

FDA registration
GIE MEDICAL·2 products·🇺🇸 United States

SHU GIE INDUSTRIAL CO., LTD.

FDA registration
SHU GIE INDUSTRIAL CO., LTD.·5 products·🇹🇼 Taiwan

GE OEC 9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 23, 2007

FLUOROSCOPIC X-RAY

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·August 30, 2007

UNK_ULTRACISION HARMONIC FOCUS

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 20, 2019

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·January 25, 2008

HARMONIC SCALPEL CURVED SHEAR (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·December 23, 2019

COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

LIGASURE

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GIE·April 23, 2021

MULTIDEBRIDER HANDPIECE, ANGLED

FDA Adverse Event
Malfunction ·GYRUS ACMI, INC·Product code GIE·July 13, 2020

MULTIDEBRIDER POWER CONSOLE

FDA Adverse Event
Malfunction ·GYRUS ACMI, INC·Product code GIE·August 12, 2020

AESCULAP

FDA Adverse Event
Injury ·AESCULAP AG·Product code GIE·September 16, 2025

BBL FIBROMETER

FDA Adverse Event
Injury ·BECTON DICKINSON MICROBIOLOGY·Product code GIE·July 14, 1995

EVIS EXERA LLL GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·February 28, 2023

MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·December 12, 2023

Fibrometer

FDA classification
FDA Class 2 ·Fibrometer

inSIGHT Ultima

FDA UDI
DIVERSATEK HEALTHCARE, INC.·B019ULT1CIED0·inSIGHT Ultima® Air-Charged Manometry System

DTE,WOODPECKER

FDA UDI
Guilin Woodpecker Medical Instrument Co., Ltd.·06944843611471·Gutta-percha injector

FUKUDA DENSHI

FDA UDI
FUKUDA DENSHI CO.,LTD.·04538612915994·

Varios

FDA UDI
NAKANISHI INC.·04560264562523·