FIAPro™ Multi-Channel Immunoflourescence Analyzer (UDI 08683548252616)
Manufactured by Vitrosens Biotechnology Inc.
Device Regulatory Overview
The FIAPro™ Multi-Channel Immunoflourescence Analyzer (Model/Catalog Number: VMFIA1002) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0201069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VMFIA1002
- Product Code / EMDN
- W0201069099
- Device Name
- Multi-Channel Immunoflourescence Analyzer
- Database Sync Date
- 2026-08-09 16:30:10
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 FIAPro™ Multi-Channel Immunoflourescence Analyzer?
The registered manufacturer of record for FIAPro™ Multi-Channel Immunoflourescence Analyzer is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for FIAPro™ Multi-Channel Immunoflourescence Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683548252616.
What classification code is assigned to this device?
This device is registered under product classification code W0201069099.
Similar Classification Devices (W0201069099)
Other Devices by Vitrosens Biotechnology Inc.
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