GUDIDData
gudid Primary ID: 0373381

QMS Zonisamide Immunoassay Calibrator (UDI 0373381)

Manufactured by Microgenics Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QMS Zonisamide Immunoassay Calibrator - Primary ID 0373381

Device Regulatory Overview

The QMS Zonisamide Immunoassay Calibrator (Model/Catalog Number: 0373381) is a medical device manufactured by Microgenics Corporation. This product is indexed under FDA Product Code / Category Classification DLJ 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-1284-2022 View Full Alert →

QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS C...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1563-2013 View Full Alert →

Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems, , Product is manufactured and distributed by Microgenics Corporatio...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0379-2013 View Full Alert →

Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO; Liquid Assayed Integrated Immunoassay Control. Intended for use as an assayed con...

🔒 Compromised Lot & Serial Numbers Locked
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Unlock Lot Data ($49)

Technical Specifications

Model Number
0373381
Product Code / EMDN
DLJ
Device Name
Database Sync Date
2026-08-09 09:45:39

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 QMS Zonisamide Immunoassay Calibrator?

The registered manufacturer of record for QMS Zonisamide Immunoassay Calibrator is Microgenics Corporation.

What is the Primary UDI-DI identifier for QMS Zonisamide Immunoassay Calibrator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0373381.

What classification code is assigned to this device?

This device is registered under product classification code DLJ.

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