Monkeypox Virus IgG Test Kit (FIA) (UDI D-VID206EW)
Manufactured by VivaChek Biotech (Hangzhou) Co., Ltd.
Device Regulatory Overview
The Monkeypox Virus IgG Test Kit (FIA) (Model/Catalog Number: VID206-01-011) is a medical device manufactured by VivaChek Biotech (Hangzhou) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105099099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VID206-01-011
- Product Code / EMDN
- W0105099099
- Device Name
- VID206
- Database Sync Date
- 2026-08-09 16:29:28
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 Monkeypox Virus IgG Test Kit (FIA)?
The registered manufacturer of record for Monkeypox Virus IgG Test Kit (FIA) is VivaChek Biotech (Hangzhou) Co., Ltd..
What is the Primary UDI-DI identifier for Monkeypox Virus IgG Test Kit (FIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-VID206EW.
What classification code is assigned to this device?
This device is registered under product classification code W0105099099.
Similar Classification Devices (W0105099099)
Other Devices by VivaChek Biotech (Hangzhou) Co., Ltd.
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