Trigger Finger | Endoscopic Trigger Finger Release (ETFR)

Instratek Inc, Endoscopic Surgical Instruments

VA Contract
Pricing Available

The Endotrig™ System
Endoscopic Trigger Finger Release (ETFR)

trigger finger release

The Endotrig™ System for Endoscopic Trigger Finger includes: a micro obturator/ cannula assembly, micro probe, micro elevator, reusable blade handle and sterilizable tray. The Endotrig™ System is designed to be used with a standard 2.3mm, 30 degree endoscope

THE ENDOTRIG™ SYSTEM

Cat #

Description

1010

1	Micro ETF Obturator
1	Micro ETF Cannula
1	Micro ETF Elevator
1	Micro Probe
1	Micro Blade Handle
1	Sterilizable tray

INDIVIDUAL COMPONENTS

1021

Micro ETF Obturator

1022

Micro ETF Cannula

1030

Micro ETF Elevator

1036

Micro Probe

1040

Micro Blade Handle

1080

Sterilizable Tray

DISPOSABLE BLADES

1052

Sterile Micro Angled Hook

1060

Sterile Biodegradable Micro Tip Swabs (5pk)

Endoscopic Trigger Finger Release, Trigger Finger, ETFR, Endotrig

Educational Resources

Call 800-892-8020 or use our contact form to receive an informational package that includes clinical study results, a demonstration video/cdrom, product brochure, and workshop information.

Proper training is strongly recommended for the most effective use of our systems.

Phone: 281-890-8020 Fax: 281-890-8068 Toll Free: 800-892-8020
210 Springhill Drive #130 ~Spring, Texas 77386

The surgical techniques presented on this web site are used to demonstrate the surgical technique by a particular practicing surgeon of the referenced product. Instratek Inc., as a manufacturer of medical devices, does not practice medicine and does not recommend these or any other surgical techniques for use on a particular patient. The surgeon who performs any surgical procedure is responsible for determining and utilizing the appropriate surgical techniques. Instratek Inc. is not responsible for the selection of the appropriate surgical technique to be used for an individual patient. Questions regarding the appropriateness of a particular technique or device should be directed to the individual patient's physician.

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