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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 PROXY — 6 UDI-DI variants, MDR

MD Atlas
Infimed Spółka z ograniczona odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Lampa operacyjna PROXY

5904384698OL03PROXYSS

6 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: 5904384698OL03PROXYSS
Device name: Lampa operacyjna PROXY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JWG1XVWZY640HVS49VWJXM3Z

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-03/0305904384698431
OL-03C05904384698424
OL-03CAM/03/03/S05904384698455
OL-03CAM/03/S05904384698448
OL-03M05904384698400
OL-03W05904384698417