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Breeze 31216201

by Dolgencorp, LLC

Breeze 31216201 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 17 Jan 2023 (UDI-DI 00090891949373), 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 Number00090891949373 UDI-DI Date17 Jan 2023ListedStatusListed 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  • Withdrawn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
Breeze
Generic name
Menstrual pad, scented
Model / reference
31216201
Primary DI / UDI-DI
00090891949373
FDA product code
NRC
GMDN term
Menstrual pad, scented
Device class
Class I
Regulation number
884.5425
GUDID distribution status
In Commercial Distribution

Related devices

Category: Menstrual pad, scented

Other devices from Dolgencorp, LLC

See all devices from Dolgencorp, LLC →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)