One Step Ovulation Test (UDI D-6909620WHSLH8KD2)
Manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.
Device Regulatory Overview
The One Step Ovulation Test (Model/Catalog Number: WH-FT-S0x0201; WH-FT-S0x0202; WH-FT-S0x0203; WH-FT-S0x0207) is a medical device manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WH-FT-S0x0201; WH-FT-S0x0202; WH-FT-S0x0203; WH-FT-S0x0207
- Product Code / EMDN
- W0102160304
- Device Name
- Ovulation Tests
- Database Sync Date
- 2026-08-09 16:30:23
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 One Step Ovulation Test?
The registered manufacturer of record for One Step Ovulation Test is W.H.P.M. Bioresearch & Technology Co., Ltd..
What is the Primary UDI-DI identifier for One Step Ovulation Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-6909620WHSLH8KD2.
What classification code is assigned to this device?
This device is registered under product classification code W0102160304.
Similar Classification Devices (W0102160304)
Other Devices by W.H.P.M. Bioresearch & Technology Co., Ltd.
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