gudid Primary ID: 23084 Trial Pack Shade B2

AxioFlow (UDI 23084 Trial Pack Shade B2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioFlow (Model/Catalog Number: 23084 Trial Pack Shade B2) 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: 23084 Trial Pack Shade B2
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 AxioFlow?

The registered manufacturer of record for AxioFlow is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioFlow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23084 Trial Pack Shade B2.

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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