Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel (UDI DUA-A1134C-008)
Manufactured by Hangzhou AllTest Biotech Co., Ltd.
Device Regulatory Overview
The Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel (Model/Catalog Number: DUA-A1134C-008) is a medical device manufactured by Hangzhou AllTest Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NGL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DUA-A1134C-008
- Product Code / EMDN
- NGL
- Device Name
- 25T, CLIA WAIVED, white package, AMP500/BAR300/BZO300/COC150/THC50/MTD300/MET500/MDMA500/MOP300/PCP25/TCA1000/OXY100/FYL1+OXI/SG/PH
- Database Sync Date
- 2026-08-09 09:22:01
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 Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel?
The registered manufacturer of record for Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel is Hangzhou AllTest Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DUA-A1134C-008.
What classification code is assigned to this device?
This device is registered under product classification code NGL.
Similar Classification Devices (NGL)
Other Devices by Hangzhou AllTest Biotech Co., Ltd.
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