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Argyle 8888261206

by Cardinalhealth

Argyle 8888261206 is a nasoenteral tube (FDA Class II; FDA product code KNT, Tubes, Gastrointestinal (and Accessories)) made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 30884521003761), 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 Number30884521003761 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Nasoenteral tube
Model / Ref / Catalog
8888261206
Primary DI / UDI-DI
30884521003761
FDA product code
KNT
GMDN term
Nasoenteral tube
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution
Size
Length — 12 Inch
Catheter Gauge — 3.5 French

Similar devices

Other devices filed under FDA product code KNT (TUBES, GASTROINTESTINAL (AND ACCESSORIES)).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

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