GUDIDData
gudid Primary ID: 2.0

ProBeam 360 Proton Therapy System - Rotating Gantry (UDI 2.0)

Manufactured by Varian Medical Systems Particle Therapy GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ProBeam 360 Proton Therapy System - Rotating Gantry - Primary ID 2.0

Device Regulatory Overview

The ProBeam 360 Proton Therapy System - Rotating Gantry (Model/Catalog Number: 2.0) is a medical device manufactured by Varian Medical Systems Particle Therapy GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2.0
Product Code / EMDN
LHN
Device Name
Database Sync Date
2026-08-09 09:49:20

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 ProBeam 360 Proton Therapy System - Rotating Gantry?

The registered manufacturer of record for ProBeam 360 Proton Therapy System - Rotating Gantry is Varian Medical Systems Particle Therapy GmbH & Co. KG.

What is the Primary UDI-DI identifier for ProBeam 360 Proton Therapy System - Rotating Gantry?

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 LHN.

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