GUDIDData
gudid Primary ID: 310600

LIAISON 25 OH Vitamin D TOTAL Assay (UDI 310600)

Manufactured by Diasorin Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIAISON 25 OH Vitamin D TOTAL Assay - Primary ID 310600

Device Regulatory Overview

The LIAISON 25 OH Vitamin D TOTAL Assay (Model/Catalog Number: 310600) is a medical device manufactured by Diasorin Inc.. This product is indexed under FDA Product Code / Category Classification MRG within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0677-2025 View Full Alert →

DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimens...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1464-2015 View Full Alert →

DiaSorin, PRO-Trac II Tacrolimus ELISA kit, REF 32400 and 32400-CN. Product Usage: The PRO-Trac II Tacrolimus ELISA kit is an in vitro rea...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1342-2021 View Full Alert →

LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended for the quantitative determination of pa...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
310600
Product Code / EMDN
MRG
Device Name
Database Sync Date
2026-08-09 09:04:28

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of LIAISON 25 OH Vitamin D TOTAL Assay?

The registered manufacturer of record for LIAISON 25 OH Vitamin D TOTAL Assay is Diasorin Inc..

What is the Primary UDI-DI identifier for LIAISON 25 OH Vitamin D TOTAL Assay?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 310600.

What classification code is assigned to this device?

This device is registered under product classification code MRG.

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