Master Medical Equipment is ISO 13485 Certified

Master Medical Equipment is determined to bring the highest quality products and services to customers around the world. A great way to showcase our dedication to these principles is by auditing our Quality Management System and our processes via a third-party company. This is why we proudly announce that MME is now ISO 13485 Certified!

ISO 13485 specifies requirements for a Quality Management System for companies to safely and efficiently handle, sell, and service medical devices. By adhering to this certification, we commit to a quality management standard of continued improvement that consistently surpasses customer and regulatory requirements.

Third-party certification demonstrates that we exceed the standard requirements. MME underwent rigorous audits with a third party to ensure processes and environments surpassed the industry standards.

What does this certification mean outside of the company? Achieving this ISO 13485:2016 certification for MME shows our commitment to being leaders in the medical device industry by holding ourselves to standards that are above and beyond our regulatory requirements. It shows our customers that we are committed to ensuring consistent quality and continually improving our processes. When working with medical devices, it’s important to remember that these are life-saving pieces of equipment, and a failure on our part to provide quality products could result in the loss of a patient’s life.

As the healthcare industry is in the national spotlight, the process of medical equipment sales and handling faces increased scrutiny. Our Quality Management System indicates our commitment to a process of continued improvement and strict adherence to protocols and processes. View our ISO 13485 Certificate here.