DrugTect Multi-Drug Urine Test Cup (UDI 1)
Manufactured by Hangzhou AllTest Biotech Co., Ltd.
Device Regulatory Overview
The DrugTect Multi-Drug Urine Test Cup (Model/Catalog Number: 1) is a medical device manufactured by Hangzhou AllTest Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- NFT
- Device Name
- 1T, EN, MOP300/MDMA500/OXY100/EDDP300/PCP25/TRA100/MET500/COC150/MTD300/BAR300/BZO300/AMP500/PPX300/TCA1000/THC50/BUP10/6-MAM10/FYL1
- Database Sync Date
- 2026-08-09 09:04:58
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 DrugTect Multi-Drug Urine Test Cup?
The registered manufacturer of record for DrugTect Multi-Drug Urine Test Cup is Hangzhou AllTest Biotech Co., Ltd..
What is the Primary UDI-DI identifier for DrugTect Multi-Drug Urine Test Cup?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code NFT.
Similar Classification Devices (NFT)
Other Devices by Hangzhou AllTest Biotech Co., Ltd.
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