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Argyle 8888501031

by Cardinal Health 200, LLC

Argyle 8888501031 is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 4 Dec 2024 (UDI-DI 10192253041569), 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 Number10192253041569 UDI-DI Date4 Dec 2024ListedStatusListed 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  • Withdrawn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
Argyle
Generic name
Surgical/emergency suction cannula, non-illuminating, single-use
Model / Ref / Catalog
8888501031
Primary DI / UDI-DI
10192253041569
FDA product code
GCX
GMDN term
Surgical/emergency suction cannula, non-illuminating, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Similar devices in this category

Other devices filed under Surgical/emergency suction cannula, non-illuminating, single-use.

Other devices from Cardinal Health 200, LLC

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Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)