Norovirus GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) (UDI 06955792734142)
Manufactured by Sansure Biotech Inc.
Device Regulatory Overview
The Norovirus GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) (Model/Catalog Number: S3220E-48) is a medical device manufactured by Sansure Biotech Inc.. This product is indexed under FDA Product Code / Category Classification W0105040516 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S3220E-48
- Product Code / EMDN
- W0105040516
- Device Name
- Norovirus GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)
- Database Sync Date
- 2026-08-09 17:33:24
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 GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)?
The registered manufacturer of record for Norovirus GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is Sansure Biotech Inc..
What is the Primary UDI-DI identifier for Norovirus GI and GII Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06955792734142.
What classification code is assigned to this device?
This device is registered under product classification code W0105040516.
Similar Classification Devices (W0105040516)
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