gudid Primary ID: 25002 Intro Pack

AxioPro ART (UDI 25002 Intro Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioPro ART (Model/Catalog Number: 25002 Intro Pack) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification EJK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 25002 Intro Pack
Product Code / EMDN: EJK
Device Name
Database Sync Date: 2026-08-09 09:01:55

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 AxioPro ART?

The registered manufacturer of record for AxioPro ART is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioPro ART?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25002 Intro Pack.

What classification code is assigned to this device?

This device is registered under product classification code EJK.

Similar Classification Devices (EJK)

Other Devices by Axiodent Inc.

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