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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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Respi.Me — 2 UDI-DI variants, MDR (Voluntis)

MD Atlas
Voluntis

Data from EUDAMED, last updated May 19, 2026

Respi.Me

376026131RESP002CT

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: Voluntis

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376026131RESP002CT
Device name: Respi.Me
Device model: 3.12
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Voluntis
SRN: FR-MF-000003043
Country: France
Email: info@voluntis.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJ02N2DPA09PXDEAK4MQ31FA

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

Respi.Me03760261310207
3.1203760261310191