eudamed_udi
Primary ID: 08685214522146
LyoSens™ (UDI 08685214522146)
Manufactured by Vitrosens Biotechnology Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LyoSens™ - Primary ID 08685214522146
Device Regulatory Overview
The LyoSens™ (Model/Catalog Number: PCR99) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105070505 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PCR99
- Product Code / EMDN
- W0105070505
- Device Name
- Viral Meningitis Genotyping qPCR Kit
- Database Sync Date
- 2026-08-09 18:41:45
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 LyoSens™?
The registered manufacturer of record for LyoSens™ is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for LyoSens™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685214522146.
What classification code is assigned to this device?
This device is registered under product classification code W0105070505.
Similar Classification Devices (W0105070505)
Other Devices by Vitrosens Biotechnology Inc.
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