Certification Requirements of Class II Prescribed Equipment
Class II Prescribed Equipment is regulated in accordance with the CNSC’s Class II Nuclear Facilities and Prescribed Equipment Regulations which specify that:
“No person shall use Class II prescribed equipment unless
- it is a certified model; or
- it is used in accordance with a licence that authorizes its use for development purposes or for scientific research that is not conducted on humans.”
The CNSC requires the certification of Class II prescribed equipment to ensure that any devices being purchased and installed are operated in accordance with the Nuclear Safety and Control Act (NSCA) and the Class II Nuclear Facilities and Prescribed Equipment Regulations. CNSC requirements for certification are independent of other requirements imposed by other federal, provincial, and territorial authorities.
Although vendors of prescribed equipment typically apply for certification, it is the licensee who is responsible for ensuring that all devices being used are certified by the CNSC. With some exceptions, device certification (or recertification) is required for:
- introduction of prescribed equipment to the Canadian market
- design change to previously certified equipment
- change in model name
- packaging or repackaging of individual certified equipment
- change in corporate ownership, name, or location.
- rebranded equipment
- changes to information previously provided for device certification
To submit your device for certification, please see the CNSC’s regulatory requirements in Certification of Radiation Devices and Class II Prescribed Equipment (RD/GD-254)
To verify that the device you are using is certified, please consult the list of CNSC Certified Class II Prescribed Equipment (PDF).
For further information please contact the CNSC:
Phone: 1-800-668-5284 or 613-995-5894