GUDIDData
gudid Primary ID: Camera head LED50-HDII

ILO (UDI Camera head LED50-HDII)

Manufactured by ILO electronic GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ILO - Primary ID Camera head LED50-HDII

Device Regulatory Overview

The ILO (Model/Catalog Number: Camera head LED50-HDII) is a medical device manufactured by ILO electronic GmbH. This product is indexed under FDA Product Code / Category Classification KQM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Camera head LED50-HDII
Product Code / EMDN
KQM
Device Name
Camera head for 1MOS HD video imaging system
Database Sync Date
2026-08-09 09:11:39

Full Regulatory Attributes

🔒 Token Gated
{
    "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 ILO?

The registered manufacturer of record for ILO is ILO electronic GmbH.

What is the Primary UDI-DI identifier for ILO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Camera head LED50-HDII.

What classification code is assigned to this device?

This device is registered under product classification code KQM.

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