Follicle-Stimulating Hormone (FSH) Menopause test

GUDID 06952062712688

This product is used for qualitative detection of Follicle-Stimulating Hormone (FSH) in the urine for women who are preparing for pregnancy and are interested in assessing their fertility. This test is designed for over-the-counter use.

ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD

Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, clinical

• Primary Device ID: 06952062712688
• NIH Device Record Key: 779bad14-9293-4d9b-b5de-91ff1061f7f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Follicle-Stimulating Hormone (FSH) Menopause test
• Version Model Number: Midstream,1pc/Box
• Company DUNS: 546403492
• Company Name: ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06952062712688 [Primary]

FDA Product Code

• NGA: Test, Follicle Stimulating Hormone (Fsh), Over The Counter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-30
• Device Publish Date: 2026-03-20

On-Brand Devices [Follicle-Stimulating Hormone (FSH) Menopause test]

• 06952062712688: This product is used for qualitative detection of Follicle-Stimulating Hormone (FSH) in the urin
• 06952062712664: This product is used for qualitative detection of Follicle-Stimulating Hormone (FSH) in the urin