eudamed_udi Primary ID: J017AWC4L400

Neoversal® (UDI J017AWC4L400)

Manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Neoversal® (Model/Catalog Number: AWC4L40) is a medical device manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AWC4L40
Product Code / EMDN: Q010699
Device Name: Artificial teeth
Database Sync Date: 2026-08-09 16:28:44

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 Neoversal®?

The registered manufacturer of record for Neoversal® is VITA Zahnfabrik H. Rauter GmbH & Co. KG.

What is the Primary UDI-DI identifier for Neoversal®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J017AWC4L400.

What classification code is assigned to this device?

This device is registered under product classification code Q010699.

Similar Classification Devices (Q010699)

Other Devices by VITA Zahnfabrik H. Rauter GmbH & Co. KG

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