Anti-Nuc Antibody CLIA Assay Kit (UDI 06975424220072)
Manufactured by DiYaLab ZJG Biotech Co., Ltd
Device Regulatory Overview
The Anti-Nuc Antibody 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 W0102100101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100 tests/kit.
- Product Code / EMDN
- W0102100101
- Device Name
- Anti-Nuc Antibody CLIA Assay Kit
- Database Sync Date
- 2026-08-09 17:21:26
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-Nuc Antibody CLIA Assay Kit?
The registered manufacturer of record for Anti-Nuc Antibody CLIA Assay Kit is DiYaLab ZJG Biotech Co., Ltd.
What is the Primary UDI-DI identifier for Anti-Nuc Antibody CLIA Assay Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424220072.
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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