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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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Vision Monitor — 8 UDI-DI variants, MDR (metrovision SAS)

MD Atlas
metrovision SAS

Data from EUDAMED, last updated May 19, 2026

Vision Monitor

5060704130VM9K

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: metrovision SAS

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 5060704130VM9K
Device name: Vision Monitor
Device model: Vision Monitor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: metrovision SAS
SRN: FR-MF-000002561
Country: France
Email: contact@metrovision.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HRVKEAPBN647P0K4W1H5TCTE

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

HVM-Ampli05060704130040
HVM-MonBaby05060704130057
HVM-MonBabyBox05060704130064
HVM-MonColor05060704130033
HVM-MonCv305060704130026
HVM-MonCvONE05060704130002
HVM-MonPackONE05060704130019
Software05060704130118