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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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Q-Las — 7 UDI-DI variants, MDR (A.R.C. Laser GmbH)

MD Atlas
A.R.C. Laser GmbH

Data from EUDAMED, last updated May 23, 2026

Q-Las

426015559Q-LAS3H

7 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: A.R.C. Laser GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426015559Q-LAS3H
Device name: Q-Las
Device model: LS09002
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: A.R.C. Laser GmbH
SRN: DE-MF-000009383
Country: Germany
Email: info@arclaser.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HJ8H931P02XB8C3X5XX2B5FX

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

LS09002-LHZO04260155590184
LS09002-LHZS04260155590207
LS09002-DVZS04260155591334
LS09002-LOSS04260155593338
LS09002-LLZS04260155593321
LS09002-DHZS04260155593314
LS09002-DVYS04260155590283