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Eddie-23-230-2-R2

by Giddy Holdings, Inc

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 Number00850013700646 UDI-DI Date5 Oct 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  • Withdrawn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
Eddie
Generic Name
Penile ring
Model / Reference
EDDIE-23-230-2-R2
Primary DI / UDI-DI
00850013700646
FDA Product Code
LKY
GMDN Term
Penile ring
Device Class
Class II
Regulation Number
876.5020
GUDID distribution status
In Commercial Distribution

Other devices from Giddy Holdings, Inc

See all devices from Giddy Holdings, Inc →

Properties

  • Sterile
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • 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