MEDICAL MURRAY PROVIDES OUR CUSTOMERS with the highest level of quality required for medical devices. We ensure the validity of all our processes, and provide consistent design, development, production and delivery of medical devices that are safe and effective.
ISO 13485:2003 and FDA Registered
All of our design and manufacturing services comply with FDA QSR 21 CFR – Part 820 and are ISO 13485:2003 Certified for design and manufacturing of Medical Devices. Our Class 7 cleanrooms are compliant with ISO 14698, Cleanrooms and associated controlled environments - Biocontamination control and ISO 14644, Cleanrooms and associated controlled environments.
Our Quality team ensures that the devices we manufacture are of the highest quality and certified to your specification. Our quality engineers are involved in the development stages of all projects to help identify and develop quality requirements, test methods and inspection requirements that are used to validate new products and processes prior to full production.
To ensure that we maintain our quality standards, we are audited each year by our notified body, TÜV SÜD. We regularly perform Internal and External auditing, and frequently support customer audits. Our current ISO 13485:2003 Certificate of Registration is for the "Design, Development and Analysis of Medical Devices along with Component Manufacturing and Assembly of Medical Devices."
Download our certificate: ISO 13485:2003
Commitment to Quality
Medical Murray is deeply committed to operation under the highest quality at every level of our company. We are dedicated to the full production of class II and class III medical devices in ISO class 7 cleanrooms at each of our locations nationwide (Illinois, North Carolina and California). We strive to design and manufacture products that meet or exceed customer requirements to help patients have a higher quality of life.