Simplifying Medical Device Management for MDR Compliance

A smarter way to stay compliant with the EU Medical Device Regulation (MDR) — without burdening healthcare staff.

Easy to use
Built for care environments
Complete device traceability

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Why MDR Matters

⚠️ MDR Is Now a Legal Requirement

The EU Medical Device Regulation (MDR 2017/745) places direct responsibility on healthcare providers — not just manufacturers — to ensure safe and traceable use of medical devices.

Healthcare organizations must:

  • Keep a complete inventory of all medical devices

  • Ensure timely maintenance, calibration, and service

  • Document usage, faults, and incidents

  • Be ready to prove compliance during inspections or audits

Non-compliance puts patient safety, staff liability, and organizational reputation at risk.

Our Solution: Alisa Medtech

The All-in-One Tool for Medical Device Management

Built in collaboration with healthcare professionals, our platform ensures full control and compliance — without complexity.

  • MDR-Ready

    Everything you need to meet EU regulatory demands, all in one system.

  • Designed for Healthcare Staff

    Intuitive, user-friendly, and accessible — no technical training needed.

  • Full Lifecycle Tracking

    From purchase to decommissioning. Schedule service, log incidents, and maintain oversight with ease.

  • Built for Real-World Care Environments

    Used in care units across Sweden, prepared for Europe. Proven in everyday healthcare operations.

Who We Help

  • Hospitals

    Simplify asset tracking and service planning

  • Elderly Care Facilities

    Empower staff to report issues, save time and stay compliant

  • Medical Technicians

    Access up-to-date service schedules and device status

  • Management & Procurement

    Gain full insight and reduce risk exposure

Alisa has truly facilitated our daily work and provides concrete benefits every day. I finally feel secure knowing we have full control, and we save so much time. It's clear that the system is developed with us users in focus. I would never want to go back to how we did things before we introduced Alisa.

— Fanny Hagström, Licensed Physiotherapist

Fanny Hagström, leg. fysioterapeut

How It Works

1

Register your devices

Easy upload or bulk import

2

Automate maintenance and alerts

Never miss a deadline

3

Log usage and faults

In just a few clicks

4

Be audit-ready

Complete traceability at your fingertips

Get Started Today

Let us show you how Alisa Medtech can simplify MDR compliance and improve patient safety in your organization.