gudid Primary ID: DLU2-1230

Lumio 2 495nm Longpass Filter (UDI DLU2-1230)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lumio 2 495nm Longpass Filter (Model/Catalog Number: DLU2-1230) is a medical device manufactured by DermLite LLC. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1506-2023 View Full Alert →

DERMLITE DL4W, REF: DL4W, Rx Only MD, CE...

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Technical Specifications

Model Number: DLU2-1230
Product Code / EMDN: KYT
Device Name: Magnetic add-on 495nm longpass filter for Lumio 2
Database Sync Date: 2026-08-09 09:37:45

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 Lumio 2 495nm Longpass Filter?

The registered manufacturer of record for Lumio 2 495nm Longpass Filter is DermLite LLC.

What is the Primary UDI-DI identifier for Lumio 2 495nm Longpass Filter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DLU2-1230.

What classification code is assigned to this device?

This device is registered under product classification code KYT.

Similar Classification Devices (KYT)

Other Devices by DermLite LLC

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