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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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LUNA 3D — 8 UDI-DI variants, MDR (LAP GmbH Laser Applikationen)

MD Atlas
LAP GmbH Laser Applikationen

Data from EUDAMED, last updated May 23, 2026

LUNA 3D

426059037SGRTD3

8 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: LAP GmbH Laser Applikationen

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426059037SGRTD3
Device name: LUNA 3D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 23, 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J3FC6VEJAC62D1D2JBKCGEMH

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

0018439-000104260590372659
001844004260590372628
001843804260590372611
0018365-000104260590372680
0018364-000904260590372598
0018364-000804260590372581
0018346-000204260590372635
0018346-000304260590372642