gudid Primary ID: HLM-9000

Auto Lensmeter HLM-9000 (UDI HLM-9000)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Auto Lensmeter HLM-9000 (Model/Catalog Number: HLM-9000) is a medical device manufactured by Huvitz Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HLM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HLM-9000
Product Code / EMDN: HLM
Device Name: Lensmeter is a machine to generate Sph, Cyl and Axis information of lens by measuring refraction of the lens
Database Sync Date: 2026-08-09 09:28:55

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 Auto Lensmeter HLM-9000?

The registered manufacturer of record for Auto Lensmeter HLM-9000 is Huvitz Co., Ltd..

What is the Primary UDI-DI identifier for Auto Lensmeter HLM-9000?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HLM-9000.

What classification code is assigned to this device?

This device is registered under product classification code HLM.

Similar Classification Devices (HLM)

Other Devices by Huvitz Co., Ltd.

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