55 results · 16ms · Sources: EU EUDAMED, US FDA

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Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.

FDA Recall
Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·September 25, 2023

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDS·October 31, 2024

EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model: GIF-HQ190

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDS·April 22, 2022

Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name: Olympus GIF-1TH190 Model/Catalog Number: GIF-1TH190 Software Version: N/A Product Description: This instrument is intended to be used with an Olympus video system center, light source, documentation equipment, monitor, EndoTherapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FDS·September 18, 2024

GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Recall
Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Recall
Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FDF·October 16, 2023

Olympus Gastrointestinal Videoscope, Model/Catalog Number: GIF-1100

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code FET·August 21, 2024

16 G / 5F Dual Lumen L-Cath catheter only.

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath Basic Kit with Introsyte

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath complete kit with U-Wing

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath Basic Kit with U-Wing

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath Basic Kit with Insyte Autoguard

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte Autoguard

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

Olympus, Model No. GIF-H180J, flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016

Olympus, Model No. GIF-H180, flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016

Olympus, Model No. GIF-160, flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016

Olympus, Model No. GIF-XP160, flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016

Olympus, Model No. GIF-Q160, flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016

Olympus, Model No. GIF-Q180,flexible scope, large diameter, video gastroscope

FDA Recall
Terminated ·Integrated Medical Systems Inc·Product code GCQ·January 20, 2016