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Argyle 888570531K

by Cardinal Health 200, LLC

Argyle 888570531K is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 2 Aug 2024 (UDI-DI 10192253057324), 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 Number10192253057324 UDI-DI Date2 Aug 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  • Withdrawn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
Closed-wound drain, non-bioabsorbable
Model / Ref / Catalog
888570531K
Primary DI / UDI-DI
10192253057324
FDA product code
JOL
GMDN term
Closed-wound drain, non-bioabsorbable
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 24 French
Length — 20 Inch

Related devices

Category: Closed-wound drain, non-bioabsorbable

Similar devices in this category

Other devices filed under Closed-wound drain, non-bioabsorbable.

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Properties

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