Providing medical devices which are able to assist clinicians and caregivers to improve patient care and outcomes is fundamental to our success. Our products are used in the treatment of millions of people around the world each year. We are continuously improving our products and the way in which they are manufactured so that we achieve the highest levels of quality and reliability.
With the healthcare device industry regulated worldwide, the ability to meet stringent standards is vital to ensuring market acceptance of our products. We assist our compliance with these standards by operating a quality management system certified to a range of international standards which apply to both our manufacturing facilities and our sales network.
As manufacturers of medical devices we are required to comply with a wide range of country specific regulations and are routinely audited for compliance to the applicable regulations. Our products destined for the United States must comply with the US Food and Drug Administration Quality System Regulation and require market clearance prior to commercialisation. Similarly, our products destined for the EU, Canada or Japan must comply with the European Medical Device Directive, CMDCAS and JPAL respectively and require country specific market clearance prior to commercialisation. Underwriters Laboratories also carry out safety tests on products designed for the US market and certify our products’ compliance with the IEC 60601-1 electrical safety standard.
We are continually developing our quality management systems to ensure that our processes and procedures meet both our business needs and changing international regulatory requirements. Continuous improvement ensures that our products and services meet the highest possible quality standards and surpass our customers’ expectations.
ISO 13485 Certificate - Mexico
ISO13485 Certificate - New Zealand
ISO 14001 Certificate