Celalux III (UDI 9090)

Manufactured by VOCO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Celalux III (Model/Catalog Number: 9090) is a medical device manufactured by VOCO GmbH. This product is indexed under FDA Product Code / Category Classification EBZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 9090
Product Code / EMDN: EBZ
Device Name: High-Power LED curing-light
Database Sync Date: 2026-08-09 09:07:36

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 Celalux III?

The registered manufacturer of record for Celalux III is VOCO GmbH.

What is the Primary UDI-DI identifier for Celalux III?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9090.

What classification code is assigned to this device?

This device is registered under product classification code EBZ.

Similar Classification Devices (EBZ)

Other Devices by VOCO GmbH

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