LyoSens CMV Detection qPCR Kit (UDI 08683548259684)
Manufactured by Vitrosens Biotechnology Inc.
Device Regulatory Overview
The LyoSens CMV Detection qPCR Kit (Model/Catalog Number: LYO42) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105040205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LYO42
- Product Code / EMDN
- W0105040205
- Device Name
- CMV Detection qPCR Kit
- Database Sync Date
- 2026-08-09 18:19:02
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 CMV Detection qPCR Kit?
The registered manufacturer of record for LyoSens CMV Detection qPCR Kit is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for LyoSens CMV Detection qPCR Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683548259684.
What classification code is assigned to this device?
This device is registered under product classification code W0105040205.
Similar Classification Devices (W0105040205)
Other Devices by Vitrosens Biotechnology Inc.
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