Australia enforces a stringent Therapeutic Goods Administration (TGA) registration process for rehabilitation medical equipment, and end‑users are eligible for government subsidies when purchasing approved wheelchairs. Through systematic assistance with qualification paperwork, Baichen enabled Sydney‑based distributor M***s to secure a place on the government‑subsidised procurement list.

Previously, M***s had lost out on multiple government contract opportunities because they lacked a full set of product compliance documents. After Baichen became involved, the team systematically provided core certifications—including CE and RoHS—and helped compile all the technical files required for TGA registration. These included EMC test reports, material safety data sheets, and product lifecycle test records. To satisfy the additional documentation demands of the government subsidy application, Baichen also supplied product performance test reports and declarations of conformity.

Following three rounds of document submissions and revisions, M***s successfully completed TGA registration, and the Baichen electric wheelchairs they distributed were officially added to the local government subsidy catalogue. The initial order of 200 units was delivered in the current quarter, and discussions for a multi‑year framework agreement are already in progress.

For overseas B2B clients, the single biggest concern when evaluating a new supplier is often “compliance risk.” Baichen’s structured document management and dedicated compliance support help clients minimise the time and expense associated with product registration, making the company a reliable partner for channel customers who supply government agencies, medical institutions, and other highly regulated end‑markets.

 Ningbo Baichen medical Devices Co.,LTD.,

+86-18058580651

Service09@baichen.ltd

www.bcwheelchair.com