gudid Primary ID: Mega Light CL

APOZA (UDI Mega Light CL)

Manufactured by APOZA ENTERPRISE CO., LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The APOZA (Model/Catalog Number: Mega Light CL) is a medical device manufactured by APOZA ENTERPRISE CO., LTD.. This product is indexed under FDA Product Code / Category Classification EBZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Mega Light CL
Product Code / EMDN: EBZ
Device Name: LED CURING LIGHT: 5W.
Database Sync Date: 2026-08-09 09:46:08

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 APOZA?

The registered manufacturer of record for APOZA is APOZA ENTERPRISE CO., LTD..

What is the Primary UDI-DI identifier for APOZA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Mega Light CL.

What classification code is assigned to this device?

This device is registered under product classification code EBZ.

Similar Classification Devices (EBZ)

Other Devices by APOZA ENTERPRISE CO., LTD.

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