Anti-SSA CLIA Assay Kit (UDI 06975424226463)
Manufactured by DiYaLab ZJG Biotech Co., Ltd
Device Regulatory Overview
The Anti-SSA CLIA Assay Kit (Model/Catalog Number: CL20132EN) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102100112 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CL20132EN
- Product Code / EMDN
- W0102100112
- Device Name
- Anti-SSA CLIA Assay Kit
- Database Sync Date
- 2026-08-09 18:46:55
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 Anti-SSA CLIA Assay Kit?
The registered manufacturer of record for Anti-SSA CLIA Assay Kit is DiYaLab ZJG Biotech Co., Ltd.
What is the Primary UDI-DI identifier for Anti-SSA CLIA Assay Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424226463.
What classification code is assigned to this device?
This device is registered under product classification code W0102100112.
Similar Classification Devices (W0102100112)
Other Devices by DiYaLab ZJG Biotech Co., Ltd
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