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Kyto KYTO2880

by Kyto Fitness Technology Co., Limited 2 variants

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 Number06978096608803 UDI-DI Date26 Feb 2025ListedStatusListed 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  • Withdrawn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
Kyto
Generic Name
Glomerular basement membrane antibody (Goodpasture antibody) IVD, reagent
Model / Reference
KYTO2880
Primary DI / UDI-DI
06978096608803
FDA Product Code
QUG
GMDN Term
Glomerular basement membrane antibody (Goodpasture antibody) IVD, reagent
Device Class
Class II
Regulation Number
874.3305
GUDID distribution status
In Commercial Distribution

Related devices

Category: Glomerular basement membrane antibody (Goodpasture antibody) IVD, reagent

Other devices from Kyto Fitness Technology Co., Limited

Properties

  • Premarket Exempt
  • Manufacturing Date

Other properties (12)

  • 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
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No