Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

0014621-000704260590370068
0014621-000804260590370075
0014621-000904260590370082
001456704260590370099
0014621-000404260590370037
0014621-000504260590370044
0014621-000604260590370051
0015562-000704260590370709
0015562-000804260590370716
0015562-000904260590370723
001408804260590370105
0015562-000404260590370679
0015562-000504260590370686
0015562-000604260590370693
0015562-000104260590370648
0015562-000204260590370655
0015562-000304260590370662
0014621-000104260590370006
0014621-000204260590370013
0014621-000304260590370020
0014622-000404260590370143
0014622-000504260590370150
0014622-000604260590370167
0014622-000104260590370112
0014622-000204260590370129

1 2 3