gudid
Primary ID: USSCupA-10M
UScreen (UDI USSCupA-10M)
Manufactured by Guangzhou Decheng Biotechnology Co., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UScreen - Primary ID USSCupA-10M
Device Regulatory Overview
The UScreen (Model/Catalog Number: USSCupA-10M) is a medical device manufactured by Guangzhou Decheng Biotechnology Co., LTD. This product is indexed under FDA Product Code / Category Classification PTG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- USSCupA-10M
- Product Code / EMDN
- PTG
- Device Name
- UScreen RAPID DRUG TEST CUP, 10-Panel, 25T/Box
- Database Sync Date
- 2026-08-09 09:31:19
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-10M.
What classification code is assigned to this device?
This device is registered under product classification code PTG.
Similar Classification Devices (PTG)
Other Devices by Guangzhou Decheng Biotechnology Co., LTD
Programmatic Export
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