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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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Suction/Irrigation HiQ - tube — 6 UDI-DI variants, MDR

MD Atlas
Olympus Winter & Ibe GmbH

Data from EUDAMED, last updated May 23, 2026

Suction/Irrigation HiQ - tube

4042761110274Y

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Olympus Winter & Ibe GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4042761110274Y
Device name: Suction/Irrigation HiQ - tube
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRGNAQ43AJSK5MVD1GYRFFW9

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

WA51151A04042761024358
WA51151L04042761024365
WA51111A04042761024297
WA51132A04042761024327
WA51131A04042761024303
WA51131L04042761024310