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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 zabiegowa ONYX — 6 UDI-DI variants, MDR

MD Atlas
Infimed Spółka z ograniczona odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Lampa zabiegowa ONYX

5904384698TL01ONYX9V

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: 5904384698TL01ONYX9V
Device name: Lampa zabiegowa ONYX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 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

basicUdiUlid01JPMFFSXNZNVKW47CQ4KJSM5N

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

TL-01-100/10005904384698554
TL-01-100C05904384698547
TL-01-100M05904384698530
TL-01-30M05904384698561
TL-01-60C05904384698523
TL-01-60M05904384698516