gudid Primary ID: 7.1.2.1

Merge PACS (UDI 7.1.2.1)

Manufactured by MERGE HEALTHCARE SOLUTIONS INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Merge PACS (Model/Catalog Number: 7.1.2.1) is a medical device manufactured by MERGE HEALTHCARE SOLUTIONS INC.. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7.1.2.1
Product Code / EMDN: LLZ
Device Name
Database Sync Date: 2026-08-09 09:00:28

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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Frequently Asked Questions

Who is the primary manufacturer of Merge PACS?

The registered manufacturer of record for Merge PACS is MERGE HEALTHCARE SOLUTIONS INC..

What is the Primary UDI-DI identifier for Merge PACS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7.1.2.1.

What classification code is assigned to this device?

This device is registered under product classification code LLZ.

Similar Classification Devices (LLZ)

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