LuxmedIQ One-Step Drug of Abuse Test (UDI D-WH-DU-S2140R01F5)
Manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.
Device Regulatory Overview
The LuxmedIQ One-Step Drug of Abuse Test (Model/Catalog Number: WH-DU-S2140R01) is a medical device manufactured by W.H.P.M. Bioresearch & Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160505 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WH-DU-S2140R01
- Product Code / EMDN
- W0102160505
- Device Name
- Drugs of Abuse Tests
- Database Sync Date
- 2026-08-09 16:50:49
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 LuxmedIQ One-Step Drug of Abuse Test?
The registered manufacturer of record for LuxmedIQ One-Step Drug of Abuse Test is W.H.P.M. Bioresearch & Technology Co., Ltd..
What is the Primary UDI-DI identifier for LuxmedIQ One-Step Drug of Abuse Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-WH-DU-S2140R01F5.
What classification code is assigned to this device?
This device is registered under product classification code W0102160505.
Similar Classification Devices (W0102160505)
Other Devices by W.H.P.M. Bioresearch & Technology Co., Ltd.
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