gudid Primary ID: 28020

Axio-Base (UDI 28020)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Axio-Base (Model/Catalog Number: 28020) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification EEA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 28020
Product Code / EMDN: EEA
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 Axio-Base?

The registered manufacturer of record for Axio-Base is Axiodent Inc..

What is the Primary UDI-DI identifier for Axio-Base?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28020.

What classification code is assigned to this device?

This device is registered under product classification code EEA.

Similar Classification Devices (EEA)

Other Devices by Axiodent Inc.

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