Labelling Requirements
Overview
All medical devices sold in Canada must carry a label meeting the requirements of the Medical Devices Regulations (ss 21–26). Labelling includes the physical label on the device and its packaging, as well as the Instructions for Use (IFU) and any accompanying documentation.
Mandatory label content
The following information must appear on the label of all medical devices (Class I–IV):
| Item | Requirement |
|---|---|
| Device name | The name under which the device is sold |
| Manufacturer name and address | Legal name and full address |
| Lot number or serial number | For traceability |
| Expiry date | Where applicable |
| Single-use designation | If intended for single use only |
| Sterility indication | If supplied sterile (must state sterilisation method) |
| Instructions for use | Adequate directions for safe use |
| Warnings and precautions | Necessary safety information |
| Storage conditions | If special storage required |
Additional content for specific device types
Implantable devices
- Implantation instructions
- Materials of construction
- MRI safety information (MR Safe / MR Conditional / MR Unsafe)
IVD devices
- Intended analyte(s) and specimen type(s)
- Performance characteristics
- Reagent composition
- Quality control requirements
- Limitations
Instructions for Use (IFU)
IFUs are part of the label. They must:
- Be written in plain language appropriate for the intended user
- Be bilingual (English and French)
- Cover intended use, contraindications, warnings, step-by-step instructions, troubleshooting, cleaning/disinfection/sterilisation
Electronic IFUs (eIFU) are permitted for certain device types consistent with IMDRF guidance. Paper IFU must still be available on request.
Legislative source: Medical Devices Regulations, SOR/98-282, ss 21–26