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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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Vitrea Read — 2 UDI-DI variants, MDR (Canon Medical Informatics A/S)

MD Atlas
Canon Medical Informatics A/S

Data from EUDAMED, last updated May 23, 2026

Vitrea Read

628105VitreaRead0017Q

2 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: Canon Medical Informatics A/S

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 628105VitreaRead0017Q
Device name: Vitrea Read
Device model: 8.4.2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: Canon Medical Informatics A/S
SRN: DK-MF-000019622
Country: Denmark
Email: sophia.mclean@mi.medical.canon

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GTJ1XWYQFFRKCS38T7YMAW2Y

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

Vitrea Read00628105001229
Vitrea Read00628105001212