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Tri-Staple 2.0 SIGCIR21XT

by Covidien LP

Tri-Staple 2.0 SIGCIR21XT is a Class II device made by Covidien LP, listed in FDA GUDID since 31 Jul 2026 (UDI-DI 10884521703797), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521703797 UDI-DI Date31 Jul 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Tri-Staple 2.0
Generic name
Surgical staple loading unit, cutting
Model / reference
SIGCIR21XT
Primary DI / UDI-DI
10884521703797
FDA product code
GAG, GDW
GMDN term
Surgical staple loading unit, cutting
Device class
Class II
Regulation number
878.4740, 878.4750
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Outer Diameter — 21 Millimeter

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See all devices from Covidien LP →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)