GUDIDData
gudid Primary ID: 1.1

Conserus Enterprise Viewer Mobile (UDI 1.1)

Manufactured by Change Healthcare Canada Company

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Conserus Enterprise Viewer Mobile - Primary ID 1.1

Device Regulatory Overview

The Conserus Enterprise Viewer Mobile (Model/Catalog Number: 1.1) is a medical device manufactured by Change Healthcare Canada Company. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1.1
Product Code / EMDN
LLZ
Device Name
Database Sync Date
2026-08-09 09:16:45

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 Conserus Enterprise Viewer Mobile?

The registered manufacturer of record for Conserus Enterprise Viewer Mobile is Change Healthcare Canada Company.

What is the Primary UDI-DI identifier for Conserus Enterprise Viewer Mobile?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.1.

What classification code is assigned to this device?

This device is registered under product classification code LLZ.

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