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nixit 00627987071368

by Nixit Limited

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 Number00627987071368 UDI-DI Date8 Jan 2019ListedStatusListed 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  • Withdrawn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
nixit
Generic Name
Menstrual cup/disc, non-latex, reusable
Model / Reference
00627987071368
Primary DI / UDI-DI
00627987071368
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

Related devices

Category: Menstrual cup/disc, non-latex, reusable

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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