eudamed_udi
Primary ID: 08683548258823
LyoSens™ (UDI 08683548258823)
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 08683548258823
Device Regulatory Overview
The LyoSens™ (Model/Catalog Number: PCR28) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105070504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PCR28
- Product Code / EMDN
- W0105070504
- Device Name
- Salmonella/Campylobacter/Shigella (EIEC) Genotyping qPCR Kit
- Database Sync Date
- 2026-08-09 16:29:13
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 08683548258823.
What classification code is assigned to this device?
This device is registered under product classification code W0105070504.
Similar Classification Devices (W0105070504)
Other Devices by Vitrosens Biotechnology Inc.
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