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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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Light Guides – Adapter — 11 UDI-DI variants, MDR

MD Atlas
Olympus Winter & Ibe GmbH

Data from EUDAMED, last updated May 23, 2026

Light Guides – Adapter

4042761110134M

11 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: Olympus Winter & Ibe GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4042761110134M
Device name: Light Guides – Adapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Olympus Winter & Ibe GmbH
SRN: DE-MF-000006729
Country: Germany
Email: eudamed.regulatoryaffairs@olympus-oste.eu

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KM8G9RCAFQT29FB1P4X8DS1H

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

A046404042761002127
WA03023A04042761062206
WA00331A04042761062299
WA03021A04042761062275
A03203A04042761029384
O033204042761000666
A320204042761004916
A320104042761004909
A046004042761002073
A033104042761001458
A321304042761004947