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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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Hicura Shaft - monopolar — 3 UDI-DI variants, MDR

MD Atlas
Olympus Winter & Ibe GmbH

Data from EUDAMED, last updated May 23, 2026

Hicura Shaft - monopolar

40427611106558

3 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 40427611106558
Device name: Hicura Shaft - monopolar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 14, 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

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP5MRRS9D1C23ZZ8YM6X0E44

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

WA69300S04042761079129
WA69300M04042761079112
WA69300L04042761079105