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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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SÜDA Move — 2 UDI-DI variants, MDR (IONTO Health & Beauty GmbH)

MD Atlas
IONTO Health & Beauty GmbH

Data from EUDAMED, last updated May 23, 2026

SÜDA Move

426011136SMC8562WL

2 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: IONTO Health & Beauty GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426011136SMC8562WL
Device name: SÜDA Move
Device model: SÜDA Move
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: IONTO Health & Beauty GmbH
SRN: DE-MF-000006268
Country: Germany
Email: info@ionto.de
Phone: +4972197700

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HBBDCH1HK06THAE2DTC7K3Y0

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

856204255583105970
856404255583113593