gudid Primary ID: 2.0

Varian Mobius Verification Phantom (UDI 2.0)

Manufactured by VARIAN MEDICAL SYSTEMS, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Varian Mobius Verification Phantom (Model/Catalog Number: 2.0) is a medical device manufactured by VARIAN MEDICAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification IXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2.0
Product Code / EMDN: IXG
Device Name
Database Sync Date: 2026-08-09 09:46:57

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 Varian Mobius Verification Phantom?

The registered manufacturer of record for Varian Mobius Verification Phantom is VARIAN MEDICAL SYSTEMS, INC..

What is the Primary UDI-DI identifier for Varian Mobius Verification Phantom?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2.0.

What classification code is assigned to this device?

This device is registered under product classification code IXG.

Similar Classification Devices (IXG)

Other Devices by VARIAN MEDICAL SYSTEMS, INC.

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