gudid Primary ID: 25009 Regular Pack

AxioCAL (UDI 25009 Regular Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioCAL (Model/Catalog Number: 25009 Regular 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: 25009 Regular 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 AxioCAL?

The registered manufacturer of record for AxioCAL is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioCAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25009 Regular 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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