gudid Primary ID: 23072 20 x 0.25g unit dose compules Shade OA3

AxioComp NT (UDI 23072 20 x 0.25g unit dose compules Shade OA3)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioComp NT (Model/Catalog Number: 23072 20 x 0.25g unit dose compules Shade OA3) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 23072 20 x 0.25g unit dose compules Shade OA3
Product Code / EMDN: EBF
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 AxioComp NT?

The registered manufacturer of record for AxioComp NT is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioComp NT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23072 20 x 0.25g unit dose compules Shade OA3.

What classification code is assigned to this device?

This device is registered under product classification code EBF.

Similar Classification Devices (EBF)

Other Devices by Axiodent Inc.

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