Medex MX6251

by ICU Medical, Inc.

Medex MX6251 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 19 Jan 2017 (UDI-DI 10351688506245), 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	Number10351688506245 UDI-DI	Date19 Jan 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10351688506245

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Medex
Generic name: Luer/Luer linear connector, single-use
Model / reference: MX6251

Primary DI / UDI-DI: 10351688506245
FDA product code: FPK
GMDN term: Luer/Luer linear connector, single-use

Device class: Class II
Regulation number: 880.5440
GUDID distribution status: In Commercial Distribution

Sterilisation method: Ethylene Oxide

Similar devices in this category

Other devices filed under Luer/Luer linear connector, single-use.

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

Supplied sterile
Sterilise before use
Single use
Prescription use
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)