UScreen (UDI USSCUPA-14CLIA)
Manufactured by Guangzhou Decheng Biotechnology Co., LTD
Device Regulatory Overview
The UScreen (Model/Catalog Number: USSCUPA-14CLIA) is a medical device manufactured by Guangzhou Decheng Biotechnology Co., LTD. This product is indexed under FDA Product Code / Category Classification PTH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- USSCUPA-14CLIA
- Product Code / EMDN
- PTH
- Device Name
- UScreen RAPID DRUG TEST CUP, 14 Panel, 25T/Box
- Database Sync Date
- 2026-08-09 09:37:39
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 UScreen?
The registered manufacturer of record for UScreen is Guangzhou Decheng Biotechnology Co., LTD.
What is the Primary UDI-DI identifier for UScreen?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is USSCUPA-14CLIA.
What classification code is assigned to this device?
This device is registered under product classification code PTH.
Similar Classification Devices (PTH)
Other Devices by Guangzhou Decheng Biotechnology Co., LTD
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