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Magellan 8881833215

by Cardinal Health 200, LLC

Magellan 8881833215 is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 17 Sep 2021 (UDI-DI 10192253024722), 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 Number10192253024722 UDI-DI Date17 Sep 2021ListedStatusListed 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  • Withdrawn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
Magellan
Generic name
Metered-delivery hypodermic syringe/needle
Model / Ref / Catalog
8881833215
Primary DI / UDI-DI
10192253024722
FDA product code
FMF
GMDN term
Metered-delivery hypodermic syringe/needle
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Metered-delivery hypodermic syringe/needle

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

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