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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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Cortrium Apex — 1 UDI-DI variant, MDR (Cortrium ApS)

MD Atlas
Cortrium ApS

Data from EUDAMED, last updated May 31, 2026

Cortrium Apex

5745000379ECG-SoftwareZ4

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: Cortrium ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5745000379ECG-SoftwareZ4
Device name: Cortrium Apex
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: Feb 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Cortrium ApS
SRN: DK-MF-000007827
Country: Denmark
Email: eudamed@cortrium.com
Phone: +45 61426077

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GSSY8FD15JVE6V2B4610A40J

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

Cortrium Apex05745000379033