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Trinity Sterile, Inc. 10039

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 10039 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 7 Feb 2023 (UDI-DI 40841767199846), 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 Number40841767199846 UDI-DI Date7 Feb 2023ListedStatusListed 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  • Withdrawn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
Trinity Sterile, Inc.
Generic name
Tourniquet cuff bandage, non-latex
Model / reference
10039
Primary DI / UDI-DI
40841767199846
FDA product code
GAX
GMDN term
Tourniquet cuff bandage, non-latex
Device class
Class I
Regulation number
878.5900
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
MRI safety
MR Unsafe

Related devices

Category: Tourniquet cuff bandage, non-latex

Other devices from Trinity Sterile, Inc.

See all devices from Trinity Sterile, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (9, all answered No)