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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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NA — 2 UDI-DI variants, MDR (Lumenis (Germany) GmbH)

MD Atlas
Lumenis (Germany) GmbH

Data from EUDAMED, last updated May 23, 2026

NA

426053918DPFXTPSNC

2 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: Lumenis (Germany) GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426053918DPFXTPSNC
Device name: —
Device model: NA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lumenis (Germany) GmbH
SRN: DE-MF-000007655
Country: Germany
Email: info.germany@lumenis.com
Phone: +49 6103 8335 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP8872A9TB4C6D1J5TQ93PQE

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

KT-1005870GR14260539182223
KT-00055555GR14260539182414