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Tampax Pure

by Procter & Gamble Manufacturing Company, the 11 variants

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 Number00073010716339 UDI-DI Date12 Aug 2022ListedStatusListed 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  • Withdrawn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
Tampax
Generic Name
Menstrual tampon, unscented
Model / Reference
Tampax Pure
Primary DI / UDI-DI
00073010716339
FDA Product Code
HEB
GMDN Term
Menstrual tampon, unscented
Device Class
Class II
Regulation Number
884.5470
GUDID distribution status
In Commercial Distribution

Related devices

Category: Menstrual tampon, unscented

Other devices from Procter & Gamble Manufacturing Company, the

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Properties

  • Single Use
  • Over-the-Counter
  • Lot / Batch Number

Other properties (11)

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