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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 Sonus Stethoscope — 13 UDI-DI variants, MDR

MD Atlas
Luxamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

LuxaScope Sonus Stethoscope

426038196StethoskopGT

13 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426038196StethoskopGT
Device name: LuxaScope Sonus Stethoscope
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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G79JJ0KME505TR1VC3NQ7SH0

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

G1.211.11204260381965121
G1.112.41404260381961390
G1.212.41404260381963899
G1.411.11404260381963677
G1.211.11404260381960928
G1.221.11404260381963660
G1.212.51404260381963905
G1.112.51404260381961468
G1.211.91404260381961963
G1.221.91404260381963707
G1.112.1404260381961383
G1.411.91404260381963684
G1.212.11404260381960874