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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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VISUCAT — 3 UDI-DI variants, MDR (IBK Systeme GmbH)

MD Atlas
IBK Systeme GmbH

Data from EUDAMED, last updated May 23, 2026

VISUCAT

426069261V00FK

3 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: IBK Systeme GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426069261V00FK
Device name: VISUCAT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: IBK Systeme GmbH
SRN: DE-MF-000006941
Country: Germany
Email: mail@ibk-systeme.de
Phone: +49 7361 923936

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNMWSYS8Y1WB927YQTAP7DK

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

VISUCAT 23,8 MH04260692610307
VISUCAT 23,8" SA04260692610352
VISUCAT 32" SA04260692610857