VIUICK (UDI 06975400320048)
Manufactured by Guangzhou Viuick Biotechnology Co.,LTD.
Device Regulatory Overview
The VIUICK (Model/Catalog Number: 48 Tests/Kit) is a medical device manufactured by Guangzhou Viuick Biotechnology Co.,LTD.. This product is indexed under FDA Product Code / Category Classification W0104080207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 48 Tests/Kit
- Product Code / EMDN
- W0104080207
- Device Name
- Diagnostic Kit for Ureaplasma Urealyticum DNA (Real-Time PCR Method)
- Database Sync Date
- 2026-08-09 17:42:43
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 VIUICK?
The registered manufacturer of record for VIUICK is Guangzhou Viuick Biotechnology Co.,LTD..
What is the Primary UDI-DI identifier for VIUICK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975400320048.
What classification code is assigned to this device?
This device is registered under product classification code W0104080207.
Similar Classification Devices (W0104080207)
Other Devices by Guangzhou Viuick Biotechnology Co.,LTD.
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