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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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ATMOS LS 21 LED — 5 UDI-DI variants, MDR

MD Atlas
ATMOS MedizinTechnik GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

ATMOS LS 21 LED

42503651ENTVisLS21R8

5 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: ATMOS MedizinTechnik GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42503651ENTVisLS21R8
Device name: ATMOS LS 21 LED
Device model: Light Sources
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 14, 2022

Manufacturer & authorised representative

Manufacturer

Name: ATMOS MedizinTechnik GmbH & Co. KG
SRN: DE-MF-000005570
Country: Germany
Email: info@atmosmed.de
Phone: +49 7653 689 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G566AM4KWTJPX992W5VFHA79

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

ATMOS LS 21 LED04250365155839
ATMOS LS 21 LED04250365170016
ATMOS LS 21 LED04250365176919
ATMOS LS 21 LED set, white04250365155860
ATMOS LS 21 LED, warm white04250365174434