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Peripheral IV Start Kit MMM-00022

by Optum Distribution Center, LLC

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 Number08500835120048 UDI-DI Date27 Apr 2026ListedStatusListed 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  • Withdrawn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
Peripheral IV Start Kit
Generic Name
Vascular catheterization support/maintenance kit, non-medicated
Model / Ref / Catalog
MMM-00022
Primary DI / UDI-DI
08500835120048
FDA Product Code
OJA
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution

Other devices from Optum Distribution Center, LLC

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Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No