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Dover 5205

by Cardinal Health 200, 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 Number10192253051629 UDI-DI Date7 Nov 2025ListedStatusListed 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  • Withdrawn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
Dover
Generic Name
Midstream urine specimen container IVD
Model / Ref / Catalog
5205, 5205-
Primary DI / UDI-DI
10192253051629
FDA Product Code
FCN
GMDN Term
Midstream urine specimen container IVD
Device Class
Class II
Regulation Number
876.5250
GUDID distribution status
In Commercial Distribution

Other devices from Cardinal Health 200, LLC

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Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No