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U by Kotex Pad

by Kimberly-Clark Global Sales, Inc. 104 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 Number00036000521313 UDI-DI Date1 Jul 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  • Withdrawn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
U by Kotex
Generic Name
Menstrual pad, unscented
Model / Reference
Pad
Primary DI / UDI-DI
00036000521313
FDA Product Code
HHD
GMDN Term
Menstrual pad, unscented
Device Class
Class I
Regulation Number
884.5435
GUDID distribution status
Not in Commercial Distribution

Other devices from Kimberly-Clark Global Sales, Inc.

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Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing 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
  • Expiration Date: No