Skip to content

U by Kotex Tampon; Pad

by Kimberly-Clark Global Sales, Inc. 2 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 Number00036000596168 UDI-DI Date18 Feb 2026ListedStatusListed 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  • Withdrawn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
U by Kotex
Generic Name
Menstrual pad, unscented
Model / Reference
Tampon, Pad
Primary DI / UDI-DI
00036000596168
FDA Product Code
HHD, HEB
GMDN Term
Menstrual pad, unscented
Models / Variants
Device Class
Class I
Regulation Number
884.5435, 884.5470
GUDID distribution status
In Commercial Distribution
Size
Weight — 9 Gram

Other devices from Kimberly-Clark Global Sales, Inc.

See all devices from Kimberly-Clark Global Sales, Inc. →

Properties

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

Other properties (10)

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