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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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Visomat — 3 UDI-DI variants, MDR (Uebe Medical GmbH)

MD Atlas
Uebe Medical GmbH

Data from EUDAMED, last updated May 31, 2026

Visomat

04023368K08199402GA

3 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: Uebe Medical GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 04023368K08199402GA
Device name: Visomat
Device model: comfort XXL, comfort form, comfort eco
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Uebe Medical GmbH
SRN: DE-MF-000005856
Country: Germany
Email: info@uebe.com
Phone: +499342924040

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMWTH63QRR7524QA2E4B1SB

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

2402804023368068006
2403804023368059004
2407804023368058007