eudamed_udi
Primary ID: 06975424222410
T3 CLIA Assay Kit (UDI 06975424222410)
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 06975424222410
Device Regulatory Overview
The T3 CLIA Assay Kit (Model/Catalog Number: 100 tests/kit) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W01020406 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100 tests/kit
- Product Code / EMDN
- W01020406
- Device Name
- T4 CLIA Assay Kit
- Database Sync Date
- 2026-08-09 16:28:59
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 06975424222410.
What classification code is assigned to this device?
This device is registered under product classification code W01020406.
Similar Classification Devices (W01020406)
Other Devices by DiYaLab ZJG Biotech Co., Ltd
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