naimNordic AI Medical

MDTPlatformInstructions for Use

Check the installed software version on the “Om MDT+” page and choose the matching instructions.

Instructions for MDTPlatform v1.0.0

IFU revision V04 (draft)

Document date: 2026-09-26

Use a PDF reader to open the instructions.

These instructions are prepared for the conformity-assessment submission. The device may be supplied for routine clinical use only after the applicable conformity assessment and declaration are complete.

Request a printed copy

Users of MDTPlatform can request a printed copy free of charge. E-mail support@nordicaimedical.com with your hospital, postal address and the IFU revision or software version you use.

The copy will be provided within seven calendar days of receiving your request. If requested when ordering the device, it will be provided at delivery.

Other editions

To request another edition, contact support@nordicaimedical.com and specify the IFU revision or software version you use.

Device identification

Device
MDTPlatform
UDI-DI
05745001289003
Basic UDI-DI
5745001289MDTPlatform2D
Manufacturer
Nordic AI Medical ApS, Slotsmarken 12, 1. th., 2970 Hørsholm, Denmark

Reporting an incident

Report any serious incident that has occurred in relation to the device to Nordic AI Medical ApS and to the competent authority of the Member State in which you or the patient are established.

Undesirable side effects not described in these instructions for use should also be reported to Nordic AI Medical ApS. Contact support@nordicaimedical.com.