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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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inmu — 4 UDI-DI variants, MDR (inmutouch.com ApS)

MD Atlas
inmutouch.com ApS

Data from EUDAMED, last updated May 31, 2026

inmu

574400089INMUSOPRANONL

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: inmutouch.com ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 574400089INMUSOPRANONL
Device name: inmu
Device model: inmu soprano
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2022

Manufacturer & authorised representative

Manufacturer

Name: inmutouch.com ApS
SRN: DK-MF-000020064
Country: Denmark
Email: info@inmutouch.com
Phone: +45 51955040

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GBR0CHPJQ4P3RVX34J1E8FB5

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

574400089006705744000890067
574400089015905744000890159
574400089014205744000890142
inmuRHYTHM05744000890197