Speak to a an expert

200

+

Medical Device Experts
1000

+

Projects
410

+

Customers
40

+

Countries
1350

+

No. of Approvals

Freyr provides comprehensive support for all Canada medical device Regulations

  • Medical Device Classification for Canada
  • Canadian Medical Device Registration Support
  • Pre-submission meetings with Health Canada
  • MDSAP
  • Medical Device Licensing (MDL)
  • Medical Device Establishment License (MDEL)
  • Canada ISED Representative
  • Medical Device Importer Solutions
  • Labeling services as per Health Canada labeling requirements for Medical Devices
  • Post Market Surveillance Support

Experience seamless approval process for Medical Devices in Canada

Book a meeting with our experts Now

Proven Success Story: How Freyr Secured Canadian Market Access for a Top US Manufacturer

Discover how Freyr’s expertise helped a leading US-based manufacturer secure Canadian market approval faster.

  • On-Time Submissions

    The Challenge

    A complex approval process.

  • Proven Track Record

    The Solution

    MDL approval + MDSAP Stage II readiness.

  • Trusted Local Expertise

    The Result

    Faster market entry, seamless compliance.

Read Full Success Story

Why Businesses choose Freyr for Canada Medical Device Approvals?

  • End-to-End Solutions

    End-to-End Solutions

    From classification to post-approval services, we provide full coverage of Health Canada medical device regulation.

  • Proven Expertise

    Proven Expertise

    We’ve helped companies navigate the complex Canada medical device regulations with precision.

  • Faster Market Access

    Faster Market Access

    Get your products to market quickly with our streamlined services for Canada medical device registration.

Frequently Asked Questions

Timelines depend on device classification and submission quality. Freyr’s streamlined process ensures faster approvals by eliminating common delays and errors.

We provide ongoing post-market surveillance, labeling updates, and compliance monitoring to keep your device market-ready and fully compliant with Health Canada’s Regulations.

If you’re manufacturing, importing, or distributing devices in Canada, an MDEL is mandatory. Freyr guides you through the application process effortlessly.

Freyr’s experts will analyze the rejection, address the issues, and resubmit with an improved strategy to ensure approval.

With 200+ experts, 1,350+ approvals, and extensive experience in 40+ countries, Freyr simplifies complex Regulatory processes to help you reach the market faster and with confidence.

Ready to launch your device in the Canadian market?

We will handle the hard part, you handle the growth, let us know your requirements in brief. Our team will get in touch with you for the best-fit solutions.