eudamed_udi
Primary ID: 08056771201018
LIAISON® Control Tg II Gen (UDI 08056771201018)
Manufactured by DiaSorin Italia S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIAISON® Control Tg II Gen - Primary ID 08056771201018
Device Regulatory Overview
The LIAISON® Control Tg II Gen (Model/Catalog Number: 317221) is a medical device manufactured by DiaSorin Italia S.p.A.. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 317221
- Product Code / EMDN
- W0102152003
- Device Name
- LIAISON® Control Tg II Gen
- Database Sync Date
- 2026-08-09 16:48:59
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 LIAISON® Control Tg II Gen?
The registered manufacturer of record for LIAISON® Control Tg II Gen is DiaSorin Italia S.p.A..
What is the Primary UDI-DI identifier for LIAISON® Control Tg II Gen?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056771201018.
What classification code is assigned to this device?
This device is registered under product classification code W0102152003.
Similar Classification Devices (W0102152003)
Other Devices by DiaSorin Italia S.p.A.
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