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Trinity Sterile, Inc. 50050

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 50050 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 25 Aug 2026 (UDI-DI 10841767195717), 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 Number10841767195717 UDI-DI Date25 Aug 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  • Withdrawn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
Irrigation syringe
Model / reference
50050
Primary DI / UDI-DI
10841767195717
FDA product code
KYZ
GMDN term
Irrigation syringe
Device class
Class I
Regulation number
880.6960
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Other devices from Trinity Sterile, Inc.

See all devices from Trinity Sterile, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (8, all answered No)