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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 Auris LED — 33 UDI-DI variants, MDR (Luxamed GmbH & Co. KG)

MD Atlas
Luxamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

LuxaScope Auris LED

426038196OtoskopYN

33 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: 426038196OtoskopYN
Device name: LuxaScope Auris LED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 6, 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

33 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G79DF5C0750FNAYB2NSA1BR9

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

A1.416.95404260381963936
A1.426.91404260381961376
A1.616.91404260381963608
A1.616.11404260381963578
A1.516.91404260381963325
A1.416.93404260381963912
A1.416.97404260381963950
A1.426.31404260381960065

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