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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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AI4CMR — 1 UDI-DI variant, MDR (AI4MedImaging Medical Solutions S.A.)

MD Atlas
AI4MedImaging Medical Solutions S.A.

Data from EUDAMED, last updated May 30, 2026

AI4CMR

5600250059SW9U

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: AI4MedImaging Medical Solutions S.A.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 5600250059SW9U
Device name: AI4CMR
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: Nov 16, 2021

Manufacturer & authorised representative

Manufacturer

Name: AI4MedImaging Medical Solutions S.A.
SRN: PT-MF-000002951
Country: Portugal
Email: calmeida@ai4cmr.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01FMM2KG429EJP79HST6MSRQZJ

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

AI4CMR05600250059015