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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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Lampa operacyjna NEXUS — 13 UDI-DI variants, MDR

MD Atlas
Infimed Spółka z ograniczona odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Lampa operacyjna NEXUS

5904384698OLNEXUS9L

13 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: Infimed Spółka z ograniczona odpowiedzialnością

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5904384698OLNEXUS9L
Device name: Lampa operacyjna NEXUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Infimed Spółka z ograniczona odpowiedzialnością
SRN: PL-MF-000015633
Country: Poland
Email: office@infimed.pl
Phone: +48 33 861 40 96

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JZQC5S4BDM9AWSY3EBY5KJSH

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

OL-01/0105904384698134
OL-01/0205904384698141
OL-01C05904384698127
OL-01CAM/01/S05904384698158
OL-01CAM/02/02/S05904384698172
OL-01CAM/02/S05904384698165
OL-01M05904384698103
OL-01W05904384698110
OL-02/0205904384698639
OL-02C05904384698622
OL-02CAM/02/S05904384698646
OL-02M05904384698608
OL-02W05904384698615