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MMS will continuously strive for industry leading reliability and quality in our products and services in the interest of patient safety, customer satisfaction and business excellence. We will comply with all applicable laws and regulations regarding the safety and efficacy of our products and we will comply with the applicable standards for our processes.
All MMS products are designed and tested to comply with European, U.S. and Canadian medical safety regulations, as well as international quality standards.
MMS complies to the following regulations and standards:
- The European Medical Device Directive 93/42/EEC
- The Quality Management Standards ISO 9001 and ISO 13485 (incl. CMDCAS)
MMS holds a Quality System Certificate and CE certificates. The certificates can be requested by sending an email to: ra@mmsinternational.com.
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