Austenal (UDI Microbond NP2)

Manufactured by Dentsply International Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Austenal (Model/Catalog Number: Microbond NP2) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EJH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Microbond NP2
Product Code / EMDN: EJH
Device Name
Database Sync Date: 2026-08-09 09:02:03

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 Austenal?

The registered manufacturer of record for Austenal is Dentsply International Inc..

What is the Primary UDI-DI identifier for Austenal?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Microbond NP2.

What classification code is assigned to this device?

This device is registered under product classification code EJH.

Similar Classification Devices (EJH)

Other Devices by Dentsply International Inc.

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