Covidien, Formerly US Surgical A Divison of Tyco H
ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY
SKU K103263UPC GDW
In Stock
—
IIFDA 510(k) Cleared (K103263)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Covidien, Formerly US Surgical A Divison of Tyco H
Free shipping on orders over $99 · 30-day returns
ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY is an FDA 510(k)-cleared medical device (K103263) manufactured by Covidien, Formerly US Surgical A Divison of Tyco H. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 21, 2010. Regulation: 8.
