Skip to content

Luteinizing Hormone (LH) Ovulation test Midstream, 1pc/Box

by Anhui Deepblue Medical Technology Co., Ltd

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06952062712671 UDI-DIDate20 Mar 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  • Withdrawn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
Luteinizing Hormone (LH) Ovulation test
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical
Model / Reference
Midstream, 1pc/Box
Primary DI / UDI-DI
06952062712671
FDA Product Code
NGE
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 Anhui Deepblue Medical Technology Co., Ltd

See all devices from Anhui Deepblue Medical Technology Co., Ltd →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No