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Fountain® 00884450028230

by Merit Medical Systems, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00884450028230 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fountain®
Generic name
Peripheral vascular intervention infusion catheter
Model / Ref / Catalog
00884450028230, IS5-90-30/A
Primary DI / UDI-DI
00884450028230
FDA product code
KRA, QEY
GMDN term
Peripheral vascular intervention infusion catheter
Device class
Class II
Regulation number
870.1210, 870.5150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral vascular intervention infusion catheter

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date

Other properties (11)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No