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Dover P4P14ULD

by Cardinal Health 200, LLC 2 variants

Dover P4P14ULD is an indwelling urethral catheterization kit (FDA Class II; FDA product code PPG, Urinary drainage collection kit) made by Cardinal Health 200, LLC, listed in FDA GUDID since 22 Aug 2024 (UDI-DI 10192253031768), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10192253031768 UDI-DI Date22 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
P4P14ULD
Primary DI / UDI-DI
10192253031768
FDA product code
PPG
GMDN term
Indwelling urethral catheterization kit, adult
Device class
Class II
Regulation number
876.5130
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 400 Milliliter
Catheter Gauge — 14 French

Related devices

Category: Indwelling urethral catheterization kit, adult

Other devices from Cardinal Health 200, LLC

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Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)