gudid Primary ID: X-MIND evo 3D

Acteon (UDI X-MIND evo 3D)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Acteon (Model/Catalog Number: X-MIND evo 3D) is a medical device manufactured by DENTAL XRAY COMPANY SRL. This product is indexed under FDA Product Code / Category Classification MUH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: X-MIND evo 3D
Product Code / EMDN: MUH
Device Name
Database Sync Date: 2026-08-09 09:04:32

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 Acteon?

The registered manufacturer of record for Acteon is DENTAL XRAY COMPANY SRL.

What is the Primary UDI-DI identifier for Acteon?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X-MIND evo 3D.

What classification code is assigned to this device?

This device is registered under product classification code MUH.

Similar Classification Devices (MUH)

Other Devices by DENTAL XRAY COMPANY SRL

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