gudid
Primary ID: 4841D2X005
Dochek (UDI 4841D2X005)
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 Dochek - Primary ID 4841D2X005
Device Regulatory Overview
The Dochek (Model/Catalog Number: 4841D2X005) is a medical device manufactured by Guangzhou Decheng Biotechnology Co., LTD. This product is indexed under FDA Product Code / Category Classification LDJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4841D2X005
- Product Code / EMDN
- LDJ
- Device Name
- Rapid Multi-drug Test Dipcard, 10-Panel
- Database Sync Date
- 2026-08-09 09:06:38
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 Dochek?
The registered manufacturer of record for Dochek is Guangzhou Decheng Biotechnology Co., LTD.
What is the Primary UDI-DI identifier for Dochek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4841D2X005.
What classification code is assigned to this device?
This device is registered under product classification code LDJ.
Similar Classification Devices (LDJ)
Other Devices by Guangzhou Decheng Biotechnology Co., LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint