LEMO UK renews ISO 13485 certification for medical device quality management

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LEMO UK is pleased to announce the successful renewal of its ISO 13485 certification, a globally recognised standard for quality management systems within the medical device industry. This accomplishment demonstrates LEMO’s dedication to upholding the highest quality and compliance standards in this specialised field.

ISO 13485 is a global standard for medical devices, addressing the entire device lifecycle, including design, production, installation, and servicing. Its purpose is to ensure the safety and effectiveness of medical devices for their intended applications.

Following the comprehensive ISO audit process with the Swiss Association for Quality and Management Systems (SQS), LEMO successfully adhered to all the necessary quality management regulations and requirements. As a result, the renewed ISO 13485 certification is valid for three years, commencing on the 16th of October 2023.

This accreditation empowers LEMO to continue advancing and enhancing its interconnection solutions and services within the expanding medical technology market. LEMO’s collaboration with customers striving to create groundbreaking medical devices is mutually advantageous, as they recognise the significance of connectors manufactured to the exacting ISO 13485 standards, saving time, and creating a clear path from innovation to the commercialisation of their products.

The renewal of ISO 13485:2016 certification is just one example of LEMO’s ongoing commitment to quality and safety in the medical device industry.

Find out more on our MEDICAL industry page