Follicle-Stimulating Hormone (FSH) Menopause test (UDI Midstream,1pc/Box)
Manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
Device Regulatory Overview
The Follicle-Stimulating Hormone (FSH) Menopause test (Model/Catalog Number: Midstream,1pc/Box) is a medical device manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD. This product is indexed under FDA Product Code / Category Classification NGA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Midstream,1pc/Box
- Product Code / EMDN
- NGA
- Device Name
- This product is used for qualitative detection of Follicle-StimulatingHormone (FSH) in the urine for women who are preparing for pregnancyand are interested in assessing their fertility. This test is designed for over-the-counter use.
- Database Sync Date
- 2026-08-09 09:05:25
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Follicle-Stimulating Hormone (FSH) Menopause test?
The registered manufacturer of record for Follicle-Stimulating Hormone (FSH) Menopause test is ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD.
What is the Primary UDI-DI identifier for Follicle-Stimulating Hormone (FSH) Menopause test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Midstream,1pc/Box.
What classification code is assigned to this device?
This device is registered under product classification code NGA.
Similar Classification Devices (NGA)
Other Devices by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
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