AED Wall Signs (Flat, Triangular or L-Shaped)

All medically classified products listed on this website meet Health Canada regulatory requirements and are subject to regular inspection to ensure they comply with the Food and Drugs Act and the Medical Devices Regulations

Please click here to view or download documents like product certifications, donning & fitting Instructions and safety data sheets.

NOTE that access to this page will require a passcode to continue. Please contact us for passcode info or if you have any difficulty accessing this information.

License Holder Listings

Health Canada (MDEL Licences) - Medical devices establishment license listing

Health Canada (MDALL Licences) - Medical devices active licenses search

Health Canada (Site Licences) - Site Licence Holders List

Health Care Professionals

Health Canada - Special Access Program

Health Care Professionals are responsible for initiating a Special Access application for situations where unlicensed medical devices are required for emergency situations, or when conventional therapies have failed, are unavailable or are unsuitable.

Guidance for Health Care Professionals on Special Access 

Request access to a medical device (Overview)

Application Form for Custom-Made Devices and Medical Devices for Special Access

Foreign Risk Notification & Monitoring

Martket regularly monitors Foreign Risk Notifications (FRNs), including recalls and safety alerts issued by regulatory agencies in other countries. This includes all countries participating in the Medical Device Single Audit Program (MDSAP), as well as the countries where medical devices imported by Martket are manufactured:

Australia - Alerts | Recalls 

Brazil - Alerts | Recalls

Canada - Alerts | Recalls

Germany - Alerts | Recalls

Japan - Alerts | Recalls

USA - Alerts | Recalls

In addition to monitoring other regulatory agencies, Martket also reviews device safety information published through the International Medical Device Regulators Forum's (IMDRF) National Competent Authority Report (NCAR) program:

IMDRF - Safety Information

Health Canada - List of regulatory agencies for the purposes of sections 61.2 and 68.3 of the Medical Devices Regulations

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Please contact us for any additional questions.