eudamed_udi
Primary ID: 08056771200493
LIAISON® NSE (UDI 08056771200493)
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® NSE - Primary ID 08056771200493
Device Regulatory Overview
The LIAISON® NSE (Model/Catalog Number: 314561) is a medical device manufactured by DiaSorin Italia S.p.A.. This product is indexed under FDA Product Code / Category Classification W0102039007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 314561
- Product Code / EMDN
- W0102039007
- Device Name
- LIAISON® NSE
- Database Sync Date
- 2026-08-09 17:45:33
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® NSE?
The registered manufacturer of record for LIAISON® NSE is DiaSorin Italia S.p.A..
What is the Primary UDI-DI identifier for LIAISON® NSE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056771200493.
What classification code is assigned to this device?
This device is registered under product classification code W0102039007.
Similar Classification Devices (W0102039007)
Other Devices by DiaSorin Italia S.p.A.
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