Monoject 5551032634

by Cardinalhealth

Monoject 5551032634 is a Class II device made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521215924), 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	Number10884521215924 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10884521215924

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Monoject
Generic name: Metered-delivery hypodermic syringe
Model / Ref / Catalog: 5551032634

Primary DI / UDI-DI: 10884521215924
FDA product code: FMF
GMDN term: Metered-delivery hypodermic syringe

Device class: Class II
Regulation number: 880.5860
GUDID distribution status: In Commercial Distribution

Size: Total Volume — 3 Milliliter
Needle Gauge — 26 Gauge

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)