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Trinity Sterile, Inc. 80359

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 80359 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 30 May 2023 (UDI-DI 10841767104870), 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 Number10841767104870 UDI-DI Date30 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  • Withdrawn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
Suture removal kit
Model / reference
80359
Primary DI / UDI-DI
10841767104870
FDA product code
MCZ
GMDN term
Suture removal kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Suture removal kit

Other devices from Trinity Sterile, Inc.

See all devices from Trinity Sterile, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (8, all answered No)