gudid Primary ID: 19009 Manual Mix Pack

AxioPex (UDI 19009 Manual Mix Pack)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioPex (Model/Catalog Number: 19009 Manual Mix Pack) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 19009 Manual Mix Pack
Product Code / EMDN: KIF
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 AxioPex?

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

What is the Primary UDI-DI identifier for AxioPex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 19009 Manual Mix Pack.

What classification code is assigned to this device?

This device is registered under product classification code KIF.

Similar Classification Devices (KIF)

Other Devices by Axiodent Inc.

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