gudid Primary ID: 1000g 27008

AxioPrint C&B Permanent (UDI 1000g 27008)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioPrint C&B Permanent (Model/Catalog Number: 1000g 27008) 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: 1000g 27008
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 AxioPrint C&B Permanent?

The registered manufacturer of record for AxioPrint C&B Permanent is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioPrint C&B Permanent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1000g 27008.

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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