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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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EO-150 VENTILATOR — 4 UDI-DI variants, MDR (EOVE SA)

MD Atlas
EOVE SA

Data from EUDAMED, last updated May 19, 2026

EO-150 VENTILATOR

376033719EO1503V

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: EOVE SA

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 376033719EO1503V
Device name: EO-150 VENTILATOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: EOVE SA
SRN: FR-MF-000002877
Country: France
Email: contact@eove.fr
Phone: +33 5 59 21 86 84

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HF6PGEQE0VYAYCDDZ198JBV6

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

AC-150VNT03760337190085
EO-150 VNT03760337190054
MV-150VNT03760337190030
VEMO 15003760337190047