Seeing Clearly, Caring Deeply, Your Partner in Animal Health

Home / All / Company News /

Jeet Medical Successfully Passing the ISO13485 Certification for Medical Devices

Jeet Medical Successfully Passing the ISO13485 Certification for Medical Devices

Nov 8,2022
The successful attainment of ISO13485 certification for our medical device quality management system underscores Jeet Medical's capability to consistently produce and deliver high-quality products and services that meet both customer and regulatory requirements. 
ISO13485 certificate
This achievement demonstrates that our processes in product design, development, manufacturing, and sales adhere to international standards. Jeet Medical rigorously implements the ISO 13485:2016 requirements, utilizing systematic, scientific, and standardized management to continuously enhance our management practices and ensure product quality. This, in turn, strengthens our product competitiveness and increases our market share.
RAE-105 stock-1
Achieving ISO13485 certification is a significant milestone in Jeet Medical's development journey, marking a critical step towards high-quality and high-standard growth. Moving forward, Jeet Medical will continue to delve deeply into the medical device field, striving to contribute significantly to China’s healthcare industry as the sector evolves.
logo of ISO13485
About ISO13485 certification

ISO13485, officially titled "Medical devices — Quality management systems — Requirements for regulatory purposes," is an independent international standard developed by the International Organization for Standardization (ISO) specifically for the medical device industry.
ISO 13485 is the quality management system standard for the medical device industry. 

Compared to ISO9001, ISO 13485 places greater emphasis on regulatory requirements, incorporating many industry-specific regulations and detailed requirements. It is the most authoritative international quality system standard for the medical device industry. 

The standard's requirements cover every phase of the medical device life cycle, including project initiation, design and development, sample preparation, registration testing, clinical evaluation, product registration, manufacturing, storage, installation or servicing, use, post-market surveillance feedback, and disposal.

Are you looking for a reliable precision endoscope manufacturer?

We can quickly provide customers with market analysis, technical support and customized services.