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Dover 24000

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 Number10192253051490 UDI-DI Date30 Sep 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  • Withdrawn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
24000
Primary DI / UDI-DI
10192253051490
FDA Product Code
FMH
GMDN Term
Midstream urine specimen container IVD
Device Class
Class I
Regulation Number
864.3250
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 4.5 Fluid Ounce

Other devices from Cardinal Health 200, LLC

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Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No