eudamed_udi
Primary ID: 08685214525901
ChainFor™ (UDI 08685214525901)
Manufactured by Vitrosens Biotechnology Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ChainFor™ - Primary ID 08685214525901
Device Regulatory Overview
The ChainFor™ (Model/Catalog Number: CFP161P50) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105070302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CFP161P50
- Product Code / EMDN
- W0105070302
- Device Name
- CNS v1.0 Genotyping qPCR Kit
- Database Sync Date
- 2026-08-09 16:28:46
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 ChainFor™?
The registered manufacturer of record for ChainFor™ is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for ChainFor™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685214525901.
What classification code is assigned to this device?
This device is registered under product classification code W0105070302.
Similar Classification Devices (W0105070302)
Other Devices by Vitrosens Biotechnology Inc.
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