Trinity Sterile, Inc. 82604

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 82604 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 28 Jul 2023 (UDI-DI 10841767104696), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10841767104696 UDI-DI	Date28 Jul 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10841767104696

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trinity Sterile, Inc.
Generic name: Vascular catheterization support/maintenance kit, non-medicated
Model / reference: 82604

Primary DI / UDI-DI: 10841767104696
FDA product code: LRP
GMDN term: Vascular catheterization support/maintenance kit, non-medicated

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Convenience kit
Premarket exempt
Lot / batch number
Serial number

Other properties (9, all answered No)