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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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Monivent Neo100 System — 1 UDI-DI variant, MDD (Monivent AB)

MD Atlas
Monivent AB

Data from EUDAMED, last updated May 31, 2026

Monivent Neo100 System

B-07340179600018

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Monivent AB

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: C001351
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: RISE Research Institutes of Sweden AB (0402)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-07340179600018
Device name: Monivent Neo100 System
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Monivent AB
SRN: SE-MF-000019004
Country: Sweden
Email: info@monivent.se
Phone: +46 (0) 31 395 48 40

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS807768WAKEQ42V88T9GDE4

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

N100-SY07340179600018