gudid Primary ID: HexaLux Light Mobile

HexaLux (UDI HexaLux Light Mobile)

Manufactured by STERIS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HexaLux (Model/Catalog Number: HexaLux Light Mobile) is a medical device manufactured by STERIS. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HexaLux Light Mobile
Product Code / EMDN: KZF
Device Name: The HexaLux Exam Mobile Light with Batteries is a powerful, next-generation LED exam light designed to be used in a multitude of rooms including the exam room, birthing suite, or intensive care unit.
Database Sync Date: 2026-08-09 09:19:08

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 HexaLux?

The registered manufacturer of record for HexaLux is STERIS.

What is the Primary UDI-DI identifier for HexaLux?

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

What classification code is assigned to this device?

This device is registered under product classification code KZF.

Similar Classification Devices (KZF)

Other Devices by STERIS

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