gudid Primary ID: 26004 Intro Pack

AxioSil Light Body (UDI 26004 Intro Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioSil Light Body (Model/Catalog Number: 26004 Intro Pack) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 26004 Intro Pack
Product Code / EMDN: ELW
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 AxioSil Light Body?

The registered manufacturer of record for AxioSil Light Body is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioSil Light Body?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26004 Intro Pack.

What classification code is assigned to this device?

This device is registered under product classification code ELW.

Similar Classification Devices (ELW)

Other Devices by Axiodent Inc.

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