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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 Handle - ratchet — 4 UDI-DI variants, MDR

MD Atlas
Olympus Winter & Ibe GmbH

Data from EUDAMED, last updated May 23, 2026

Hicura Handle - ratchet

40427611106252

4 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

Reusable

Identity & classification

Basic UDI-DI: 40427611106252
Device name: Hicura Handle - ratchet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP5MR2VV9SJRWMNW089PA1R1

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

WA69000L04042761078269
WA69003L04042761078320
WA69000M04042761078276
WA69003M04042761078337