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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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Operating Light — 6 UDI-DI variants, MDR (SternMed GmbH)

MD Atlas
SternMed GmbH

Data from EUDAMED, last updated May 23, 2026

Operating Light

42517308015L7

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: SternMed GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42517308015L7
Device name: Operating Light
Device model: Lumax 25 / Lumax 15 / Lumax 5 / Lumax 3/ Lumax 3M / Lumax 1M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2023

Manufacturer & authorised representative

Manufacturer

Name: SternMed GmbH
SRN: DE-MF-000015421
Country: Germany
Email: info@sternmed.de
Phone: +49 757 35978 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G0CGDHG85AENDFMK5G1KGKS8

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

310120004251730810414
310010304251730810421
310125004251730810407
310115004251730800040
310110004251730800507
310010504251730810438