Luteinizing Hormone (LH) Ovulation test (UDI Strip,1pc/Box)
Manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
Device Regulatory Overview
The Luteinizing Hormone (LH) Ovulation test (Model/Catalog Number: Strip,1pc/Box) is a medical device manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD. This product is indexed under FDA Product Code / Category Classification NGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Strip,1pc/Box
- Product Code / EMDN
- NGE
- Device Name
- LH Ovulation Test (Colloidal Gold) is a rapid chromatographicimmunoassay for the qualitative detection of Luteinising Hormone (LH) in female urine to predict when there is a LH surge, and in turn, when you arelikely to ovulate. 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 Luteinizing Hormone (LH) Ovulation test?
The registered manufacturer of record for Luteinizing Hormone (LH) Ovulation test is ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD.
What is the Primary UDI-DI identifier for Luteinizing Hormone (LH) Ovulation test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Strip,1pc/Box.
What classification code is assigned to this device?
This device is registered under product classification code NGE.
Similar Classification Devices (NGE)
Other Devices by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
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