The Therapeutic Goods Administration (TGA), a division of the Australian Department of Health, is the regulatory body for therapeutic goods (including medicines, medical devices, gene technology, and blood products) in Australia. Australia is well-known of its high standard as well as restriction in medical devices. The current level of Australian TGA standard is equivalent to EU and the Asia-Pacific region (more than 30 countries). TGA is highly recognized within the Australia and its standard can be regarded as the highest internationally.
As the first manufacturer of oxygen generation system in Australia, Meditech is renowned in Australia for its outstanding sales and service scheme, diversified market channels as well as excellent brand awareness, and therefore highly recognized in the oxygen supply industry. All product series from Meditech have now successfully been granted with three TGA certificates in Australia. This is the official certification of the highest level medical regulations after the China CFDA and the German TUV ISO13485 certification.
Obtaining the TGA certification indicates that the quality of the product of Meditech is fully recognized by the Australian government and more than 20 countries including France, Germany and Singapore in the PIC/S member countries. Meditech has been able to develop the high standardization process of innovation, R&D, production and service. These provide safer, more effective and more reliable medical oxygen equipment with the highest standard. At the same time, Ausmedi has been granted the German TUV ISO13485 certification. The novel designs, concepts, technical advancement have laid a solid foundation for our global reach in the near future.