Skip to content

Flo 1

by Co-Innovation Biotech Co., Ltd GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06970429844124 UDI-DIDate31 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Flo
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical
Model / Reference
1
Primary DI / UDI-DI
06970429844124
FDA Product Code
CEP
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical
Device Class
Class I
Regulation Number
862.1485
GUDID distribution status
In Commercial Distribution

Other devices from Co-Innovation Biotech Co., Ltd

See all devices from Co-Innovation Biotech Co., Ltd →

Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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