gudid Primary ID: 25004 Trial Pack

AxioCAL LC (UDI 25004 Trial Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioCAL LC (Model/Catalog Number: 25004 Trial 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: 25004 Trial 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 LC?

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

What is the Primary UDI-DI identifier for AxioCAL LC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25004 Trial 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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