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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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LuxaScope Oculus LED — 11 UDI-DI variants, MDR (Luxamed GmbH & Co. KG)

MD Atlas
Luxamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

LuxaScope Oculus LED

426038196OphthalmoskopZH

11 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: Luxamed GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426038196OphthalmoskopZH
Device name: LuxaScope Oculus LED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Luxamed GmbH & Co. KG
SRN: DE-MF-000006437
Country: Germany
Email: info@luxamed.de
Phone: 07344/9290510

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GM5TXP75V40C87XSCJWFTCRX

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

F1.516.91404260381964520
F1.416.95404260381964407
F1.416.93404260381964384
F1.416.11404260381964315
F1.426.11404260381964339
F1.416.97404260381964421
F1.426.91404260381964346
F1.416.96404260381964414
F1.416.91404260381964322
F1.416.11204260381965466
LuxaScope Oculus 2.5V, white/colza yellow04260381964391