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Trinity Sterile, Inc. 6000

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 6000 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 2 May 2023 (UDI-DI 10841767103767), 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 Number10841767103767 UDI-DI Date2 May 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  • Withdrawn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
Dressing/utility forceps, scissors-like, single-use
Model / reference
6000
Primary DI / UDI-DI
10841767103767
FDA product code
HXK
GMDN term
Dressing/utility forceps, scissors-like, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Dressing/utility forceps, scissors-like, single-use

Similar devices in this category

Other devices filed under Dressing/utility forceps, scissors-like, single-use.

Other devices from Trinity Sterile, Inc.

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Properties

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