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Accu-Clear OVULATION TEST

by Procter & Gamble Manufacturing Company, the

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 Number00633472601958 UDI-DIDate11 Nov 2020ListedStatusListed 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  • Withdrawn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
Accu-Clear
Generic Name
Natural conception assistance kit
Model / Reference
OVULATION TEST
Primary DI / UDI-DI
00633472601958
FDA Product Code
NGE
GMDN Term
Natural conception assistance kit
Device Class
Class I
Regulation Number
862.1485
GUDID distribution status
Not in Commercial Distribution

Other devices from Procter & Gamble Manufacturing Company, the

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Properties

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

Other properties (9)

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