Importing and registering pill presses (designated devices)

Overview

This guidance document provides an overview of what you need to do to import a designated device to Canada commercially, including:

• general requirements for registration
• import requirements
• import procedures and documents

Who this guide is for

• Pharmaceutical, Food and consumer product industry
• Individuals thinking about becoming importers of designated devices
• Individuals planning to import a designated device

In this guide

• Definition of designated device
• Registration requirements
• Declaration of legitimate uses
• Process to register a designated device and/or component parts
• Required information for registering a designated device and component part
• Importers must provide proof of registration of the designated device or component part to border officials
• Registration process and timelines
• Submission of the registration form
• Consequences of not registering a designated device before importation
• Questions or comments regarding the registration process

View complete guide

Details and history

Published: January 27, 2026
Part of topic(s): Canadian Drugs and Substances Strategy

For assistance

Contact the Authorizations Division if you need assistance:

By e-mail: authorizations-autorisations@hc-sc.gc.ca

Health Canada's service hours are Monday to Friday from 8 am to 6 pm (Eastern time). They are closed on statutory holidays.