Trinity Sterile, Inc. 85388

by Trinity Sterile, Inc.

Trinity Sterile, Inc. 85388 is a Class II device made by Trinity Sterile, Inc., listed in FDA GUDID since 31 Jan 2023 (UDI-DI 10841767107871), 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	Number10841767107871 UDI-DI	Date31 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10841767107871

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Trinity Sterile, Inc.
Generic name: Basic intravenous administration set, noninvasive
Model / reference: 85388

Primary DI / UDI-DI: 10841767107871
FDA product code: LRS
GMDN term: Basic intravenous administration set, noninvasive

Device class: Class II
Regulation number: 880.5200
GUDID distribution status: In Commercial Distribution

Sterilisation method: Ethylene Oxide
MRI safety: MR Unsafe

Similar devices in this category

Other devices filed under Basic intravenous administration set, noninvasive.

Other devices from Trinity Sterile, Inc.

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Properties

Supplied sterile
Sterilise before use
Single use
Convenience kit
Lot / batch number
Serial number

Other properties (9, all answered No)