gudid Primary ID: 26012 50ml Regular Set

AxioSil Heavy Body (UDI 26012 50ml Regular Set)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioSil Heavy Body (Model/Catalog Number: 26012 50ml Regular Set) 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: 26012 50ml Regular Set
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 Heavy Body?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26012 50ml Regular Set.

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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