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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Light source — 3 UDI-DI variants, MDR (Erbe Vision GmbH)

MD Atlas
Erbe Vision GmbH

Data from EUDAMED, last updated May 23, 2026

Light source

426021465000IlluminateW8

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Erbe Vision GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426021465000IlluminateW8
Device name: Light source
Device model: Light source
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Erbe Vision GmbH
SRN: DE-MF-000010268
Country: Germany
Email: prrc@erbe-vision.com
Phone: +49 7461 908460

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HZRTX9SGHZDXTVQZ46B241CG

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LED 610 Light source04260214650194
LUMOS LED Light Source WL & NIR04260386576902
X-Light04260214650200