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Careflow™ 10884450321819

by Argon Critical Care Systems Singapore Pte. Ltd.

Careflow™ 10884450321819 (681703/A) is a Class II device made by Argon Critical Care Systems Singapore Pte. Ltd., listed in FDA GUDID since 15 Oct 2018 (UDI-DI 10884450321819), 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 Number10884450321819 UDI-DI Date15 Oct 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  • Withdrawn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
Careflow™
Generic name
Central venous catheterization kit, short-term
Model / Ref / Catalog
10884450321819, 681703/A
Primary DI / UDI-DI
10884450321819
FDA product code
FOZ
GMDN term
Central venous catheterization kit, short-term
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Central venous catheterization kit, short-term

Other devices from Argon Critical Care Systems Singapore Pte. Ltd.

See all devices from Argon Critical Care Systems Singapore Pte. Ltd. →

Properties

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