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Follicle-Stimulating Hormone (FSH) Menopause test Midstream, 1pc/Box

by Anhui Deepblue Medical Technology Co., Ltd GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06952062712688 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  • Withdrawn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

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Follicle-Stimulating Hormone (FSH) Menopause test
Generic Name
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, clinical
Model / Reference
Midstream, 1pc/Box
Primary DI / UDI-DI
06952062712688
FDA Product Code
NGA
GMDN Term
Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, clinical
Device Class
Class I
Regulation Number
862.1300
GUDID distribution status
In Commercial Distribution

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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