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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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Laser patient positioning system — 65 UDI-DI variants, MDR

MD Atlas
LAP GmbH Laser Applikationen

Data from EUDAMED, last updated May 23, 2026

Laser patient positioning system

426059037PATPOSLASERCR

65 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: LAP GmbH Laser Applikationen

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426059037PATPOSLASERCR
Device name: Laser patient positioning system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: LAP GmbH Laser Applikationen
SRN: DE-MF-000005792
Country: Germany
Email: info@lap-laser.com
Phone: +49 4131 9511 95

Variants by status

UDI-DI variants

65 UDI-DI variants

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Applied filters

basicUdiUlid01HW2XQNMY76WVC88JS5BD7F3W

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

No registered UDI-DI variants for this device family.