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Saalt Menstrual Disc SD0003R

by Saalt, LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810050724241 UDI-DI Date13 Jul 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  • Withdrawn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
Saalt Menstrual Disc
Generic Name
Menstrual cup/disc, non-latex, reusable
Model / Reference
SD0003R
Primary DI / UDI-DI
00810050724241
FDA Product Code
HHE
GMDN Term
Menstrual cup/disc, non-latex, reusable
Device Class
Class II
Regulation Number
884.5400
GUDID distribution status
In Commercial Distribution

Other devices from Saalt, LLC

See all devices from Saalt, LLC →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No