Alltest Multi-Drug 4 Drugs Rapid Test Cup (Urine) (UDI 1)
Manufactured by Hangzhou AllTest Biotech Co., Ltd.
Device Regulatory Overview
The Alltest Multi-Drug 4 Drugs Rapid Test Cup (Urine) (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 NGL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- NGL
- Device Name
- 25T, FDA CLIA waived, MDMA500/OXY100/PCP25/BUP10
- Database Sync Date
- 2026-08-09 09:04:58
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Alltest Multi-Drug 4 Drugs Rapid Test Cup (Urine)?
The registered manufacturer of record for Alltest Multi-Drug 4 Drugs Rapid Test Cup (Urine) is Hangzhou AllTest Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Alltest Multi-Drug 4 Drugs Rapid Test Cup (Urine)?
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 NGL.
Similar Classification Devices (NGL)
Other Devices by Hangzhou AllTest Biotech Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint