Yuyue uses SOC chip technology to make blood pressure measurement accurate.
Features and functions of SOC chips:
1. High-performance processing power
SOC chips have powerful processing power to quickly process and analyze data obtained from sensors. This enables the device to measure and calculate blood pressure values in real time, providing accurate measurement results.
2. High-precision sensor interface
The SOC chip is equipped with a high-precision sensor interface that can accurately read data from the blood pressure sensor. This ensures that the device is able to acquire accurate blood pressure signals, which in turn provides accurate blood pressure measurements.
3. Advanced Algorithms and Computational Models
The SOC chipset integrates advanced algorithms and computational models to accurately analyze and process blood pressure signals. These algorithms and models can eliminate interfering factors and provide accurate blood pressure measurement results.
4. Low-power design
The SOC chip utilizes a low-power design to reduce power consumption while maintaining performance. This not only extends the battery life of the device, but also provides stable and long-lasting blood pressure monitoring.
Medical device R&D standards:
1. ISO 13485
This is the global international standard for quality management systems for medical devices. It defines the quality management requirements that medical device manufacturers should follow, including design, development, production, installation and after-sales service.
2. ISO 14971
This is the international standard for risk management of medical devices. It requires manufacturers to assess and manage risks throughout the life cycle of a medical device, including design, development, production, use and maintenance.
3. FDA 510(k)
This is the U.S. Food and Drug Administration's (FDA) pre-market approval requirement for medical devices. Manufacturers are required to submit a 510(k) application to demonstrate that their new medical device has a similar safety and efficacy profile as a similar device that has already been approved.
4. CE marking
This is the European Union's market access certification for medical devices. With CE marking, manufacturers demonstrate that their medical devices meet the safety, efficacy and quality requirements of the EU.
5. GMP requirements
This is Good Manufacturing Practice for the production of pharmaceuticals and medical devices. Manufacturers need to follow GMP requirements to ensure consistency, traceability and reliability in the production of medical devices.
6. IEEE Standards
This is a series of standards published by the Institute of Electrical and Electronics Engineers (IEEE) that cover aspects of medical device design, safety, and communication.