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Trinity Sterile, Inc. 5007M

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 5007M is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 6 Oct 2026 (UDI-DI 10841767100537), 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 Number10841767100537 UDI-DI Date6 Oct 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  • Withdrawn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
Trinity Sterile, Inc.
Generic name
General-purpose surgical scissors, single-use
Model / reference
5007M
Primary DI / UDI-DI
10841767100537
FDA product code
LRW
GMDN term
General-purpose surgical scissors, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

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
  • Expiration date
Other properties (7, all answered No)