Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing) (UDI 06974674892633)
Manufactured by Shenzhen Zijian Biotechnology Co., Ltd
Device Regulatory Overview
The Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing) (Model/Catalog Number: 18-01-0023) is a medical device manufactured by Shenzhen Zijian Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0105040516 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 18-01-0023
- Product Code / EMDN
- W0105040516
- Device Name
- Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing)
- Database Sync Date
- 2026-08-09 19:05:05
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 Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing)?
The registered manufacturer of record for Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing) is Shenzhen Zijian Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for Norovirus type GI/GII Diagnostic Kit (PCR-Fluorescence Probing)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974674892633.
What classification code is assigned to this device?
This device is registered under product classification code W0105040516.
Similar Classification Devices (W0105040516)
Other Devices by Shenzhen Zijian Biotechnology Co., Ltd
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