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POWERWAND Max Barrier Kit 4Fr X 8cm

by Access Scientific, 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 Number10859821006299 UDI-DI Date9 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  • Withdrawn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
Powerwand
Generic name
Peripheral vascular catheter
Model / Ref / Catalog
Max Barrier Kit 4Fr X 8cm, 72390
Primary DI / UDI-DI
10859821006299
FDA product code
OWL
GMDN term
Peripheral vascular catheter
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution
Size
Length — 8 Centimeter
Catheter Gauge — 4 French

Related devices

Category: Peripheral vascular catheter

Other devices from Access Scientific, Inc.

See all devices from Access Scientific, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date

Other properties (9)

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