gudid
Primary ID: 311460
LIAISON SARS-CoV-2 S1/S2 IgG (UDI 311460)
Manufactured by DIASORIN SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIAISON SARS-CoV-2 S1/S2 IgG - Primary ID 311460
Device Regulatory Overview
The LIAISON SARS-CoV-2 S1/S2 IgG (Model/Catalog Number: 311460) is a medical device manufactured by DIASORIN SPA. This product is indexed under FDA Product Code / Category Classification QKO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 311460
- Product Code / EMDN
- QKO
- Device Name
- Database Sync Date
- 2026-08-09 09:04:28
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 SARS-CoV-2 S1/S2 IgG?
The registered manufacturer of record for LIAISON SARS-CoV-2 S1/S2 IgG is DIASORIN SPA.
What is the Primary UDI-DI identifier for LIAISON SARS-CoV-2 S1/S2 IgG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 311460.
What classification code is assigned to this device?
This device is registered under product classification code QKO.
Similar Classification Devices (QKO)
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