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Monoject 8881305117

by Cardinalhealth

Monoject 8881305117 is a Class I device made by Cardinalhealth, listed in FDA GUDID since 27 Jun 2018 (UDI-DI 10884521012622), 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 Number10884521012622 UDI-DI Date27 Jun 2018ListedStatusListed 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  • Withdrawn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
Monoject
Generic name
Medication transfer needle, filtering
Model / Ref / Catalog
8881305117
Primary DI / UDI-DI
10884521012622
FDA product code
GAA
GMDN term
Medication transfer needle, filtering
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Length — 1.50 Inch

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)