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Hemodialysis Pack 500326D

by Argon Medical Devices, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886333215843 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Hemodialysis Pack
Generic name
General surgical procedure kit, medicated
Model / Ref / Catalog
500326D
Primary DI / UDI-DI
00886333215843
FDA product code
PPI
GMDN term
General surgical procedure kit, medicated
Device class
Class II
Regulation number
876.5820
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (6)

  • Sterilise before use: No
  • Implantable: No
  • Over-the-counter: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No