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Dover 6153

by Cardinal Health 200, LLC 4 variants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521015258 UDI-DI Date24 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  • Withdrawn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
Dover
Generic Name
Indwelling urethral catheterization kit, adult
Model / Ref / Catalog
6153, 6153-
Primary DI / UDI-DI
10884521015258
FDA Product Code
PPG
GMDN Term
Indwelling urethral catheterization kit, adult
Device Class
Class II
Regulation Number
876.5130
GUDID distribution status
Not in Commercial Distribution
Size
Catheter Gauge — 16 French
Total Volume — 2000 Milliliter

Related devices

Category: Indwelling urethral catheterization kit, adult

Other devices from Cardinal Health 200, LLC

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Properties

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

Other properties (6)

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