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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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Umschaltstation redox. autoswitch — 2 UDI-DI variants, MDR

MD Atlas
hestomed GmbH

Data from EUDAMED, last updated May 23, 2026

Umschaltstation redox. autoswitch

426066638autoswitch7Y

2 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: hestomed GmbH

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 426066638autoswitch7Y
Device name: Umschaltstation redox. autoswitch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: hestomed GmbH
SRN: DE-MF-000006850
Country: Germany
Email: f.wagner@hestomed.de
Phone: 03720463818

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGKWEE85AX76VEGSPWV96RMR

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

switching system redox. autoswitch, AIR04260666389642
switching system redox. autoswitch, O204260666389635