eudamed_udi
Primary ID: 06975424228764
T3 CLIA Assay Kit (UDI 06975424228764)
Manufactured by DiYaLab ZJG Biotech Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for T3 CLIA Assay Kit - Primary ID 06975424228764
Device Regulatory Overview
The T3 CLIA Assay Kit (Model/Catalog Number: CL21031E) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W01020405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CL21031E
- Product Code / EMDN
- W01020405
- Device Name
- T3 CLIA Assay Kit
- Database Sync Date
- 2026-08-09 16:46:50
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 T3 CLIA Assay Kit?
The registered manufacturer of record for T3 CLIA Assay Kit is DiYaLab ZJG Biotech Co., Ltd.
What is the Primary UDI-DI identifier for T3 CLIA Assay Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424228764.
What classification code is assigned to this device?
This device is registered under product classification code W01020405.
Similar Classification Devices (W01020405)
Other Devices by DiYaLab ZJG Biotech Co., Ltd
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