November 10, 2025
Canada Medical Device Registration Process & Classifications
Planning to sell your medical device in Canada?
Health Canada is the government body that reviews and approves all medical devices before they can be marketed in the country. Their goal is simple — to make sure all devices are safe, effective, and high quality.
If you are a manufacturer, importer, or distributor, you must understand how Health Canada classifies medical devices and what kind of licence you need.
At OMC Medical, we help companies like yours register their devices smoothly — from the first classification step to final approval.
Canada classifies medical devices based on risk — from Class I (low risk) to Class IV (high risk).
Correct classification determines your licensing route, technical documentation, and review timeline.
| Class | Risk Level | Example Devices | Licence Type |
| Class I | Low | Bandages, hospital beds | MDEL (Establishment Licence) |
| Class II | Low–Moderate | Contact lenses, hearing aids | MDL (Device Licence) |
| Class III | Moderate–High | Orthopedic implants, infusion pumps | MDL |
| Class IV | High | Pacemakers, heart valves | MDL |
📘 Health Canada – Medical Devices Regulations
Required for:
Key Points:
Required for:
You’ll need to submit:
Check the official listing of approved devices here: MDALL Database
Here’s a clear breakdown of how to register a medical device in Canada:
Check Health Canada’s official definition — it covers anything used to diagnose, treat, or prevent diseases or abnormal conditions.
Use the classification rules to find out whether it’s Class I, II, III, or IV.
If unsure, OMC Medical can help with proper classification.
For MDL applications:
For MDEL applications:
Applications are submitted through Health Canada’s official forms and email channels.
Health Canada reviews your application and may ask for clarifications.
Once approved, your device appears on the Medical Devices Active Licence Listing (MDALL) database.
| ✅ | Step | Assistance from OMC Medical |
| ☐ | Identify product as a medical device | Regulatory assessment |
| ☐ | Determine device classification (I–IV) | Classification guidance |
| ☐ | Identify required licence (MDEL / MDL) | Licence strategy planning |
| ☐ | Prepare technical documentation | File preparation & review |
| ☐ | ISO 13485 / QMS support | QMS setup & certification |
| ☐ | Complete Health Canada forms | Application assistance |
| ☐ | Submit application | Submission coordination |
| ☐ | Respond to Health Canada queries | Liaison & clarification |
| ☐ | Receive licence approval | Verification in MDALL |
| ☐ | Maintain post-market compliance | Ongoing regulatory support |
At OMC Medical, we simplify the entire Health Canada registration process. Our team of regulatory experts provides:
💬 “With OMC Medical, your path to the Canadian market becomes clear, compliant, and confident.”
The Canada medical device registration process is structured but manageable when approached with the right knowledge and partner.
By classifying your device correctly, preparing strong documentation, and maintaining compliance, you can access one of the world’s safest and most trusted healthcare markets.
Let OMC Medical handle the complexities — so you can focus on innovation and business growth.
📩 Get in touch with our team today to start your Canada registration journey.
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