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Intimina Ziggy Cup 6140

by Leloi AB

Intimina Ziggy Cup 6140 is a Class II device made by Leloi AB, listed in FDA GUDID since 7 Nov 2017 (UDI-DI 07350075026140), 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 Number07350075026140 UDI-DI Date7 Nov 2017ListedStatusListed 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  • Withdrawn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
Intimina Ziggy Cup
Generic name
Menstrual cup/disc, non-latex, reusable
Model / reference
6140
Primary DI / UDI-DI
07350075026140
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

Similar devices

Other devices filed under FDA product code HHE (Cup, Menstrual).

Other devices from Leloi AB

See all devices from Leloi AB →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)