EUROLAB laboratory provides testing and compliance service within the scope of CAN CSA-C22.2 No.601.1-M90 standard. This standard applies to the safety of medical electrical equipment designed to be installed and used in accordance with Canadian Electrical Code part I rules.
While this standard is primarily safety-related, it contains some requirements for reliable operation where it is safety-related.
Safety hazards arising from the intended physiological function of equipment covered by this standard are not considered. This standard is also applicable to equipment used for the compensation or alleviation of diseases. In vitro diagnostic equipment that does not fall within the definition of ME equipment is covered by the IEC 61010 series.
This standard does not apply to the implantable parts of active implantable medical devices within the scope of ISO 14708-1-3. The purpose of this standard is to specify general requirements and to form the basis for specific standards.
EUROLAB assists manufacturers with CAN CSA-C22.2 No.601.1-M90 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
