EPT Menopause (FSH) Rapid Test FFS-103H

GUDID 50045611954019

Hangzhou AllTest Biotech Co., Ltd.

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

• Primary Device ID: 50045611954019
• NIH Device Record Key: fa7231db-eb31-4725-b40f-332fb8d8bc53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EPT Menopause (FSH) Rapid Test
• Version Model Number: 95401-4
• Catalog Number: FFS-103H
• Company DUNS: 543254717
• Company Name: Hangzhou AllTest Biotech Co., Ltd.
• Device Count: 3
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	20045611954018 [Primary]
GS1	50045611954019 [Unit of Use]

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: 2025-12-18
• Device Publish Date: 2025-12-10

Devices Manufactured by Hangzhou AllTest Biotech Co., Ltd.

• 50045611954019 - EPT Menopause (FSH) Rapid Test: 2025-12-18
• 50045611954019 - EPT Menopause (FSH) Rapid Test: 2025-12-18
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