ANA Screening Antibody CLIA Assay Kit (UDI 06975424226913)
Manufactured by DiYaLab ZJG Biotech Co., Ltd
Device Regulatory Overview
The ANA Screening Antibody CLIA Assay Kit (Model/Catalog Number: CL30422EN) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102100101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CL30422EN
- Product Code / EMDN
- W0102100101
- Device Name
- ANA Screening Antibody CLIA Assay Kit
- Database Sync Date
- 2026-08-09 17:04:28
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 ANA Screening Antibody CLIA Assay Kit?
The registered manufacturer of record for ANA Screening Antibody CLIA Assay Kit is DiYaLab ZJG Biotech Co., Ltd.
What is the Primary UDI-DI identifier for ANA Screening Antibody CLIA Assay Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424226913.
What classification code is assigned to this device?
This device is registered under product classification code W0102100101.
Similar Classification Devices (W0102100101)
Other Devices by DiYaLab ZJG Biotech Co., Ltd
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