Device Manufacturer

If there is no forward tilting action and other actions are present, then the compression pump is working normally, but the corresponding membrane switch is faulty or the corresponding solenoid valve is faulty.

The surgeon in the operating room must be able to accurately distinguish contours, colors and movements.

There are more water molecules in the air, and the whole environment is filled with the smell of humidity, which is likely to cause the equipment to become moldy and damp.

Inspection of the mechanical installation of the surgical shadowless lamp: Check whether there are any mechanical installation defects, whether there are missing screws or not tight screws.

After the operation is performed in the operating room, the incision is not sutured.

The configuration of the single-head surgical shadowless lamp is lower than that of the double-female lamp, but its price and performance can be used in general outpatient clinics, caesarean sections, emergency rooms and some obstetric medical service institutions.

The composition of the electric delivery bed is composed of mechanical and electrical control systems, which are divided into 24 models according to their functions.

The closer the color rendering index of the surgical shadowless lamp is to the sunlight, the higher the color reproduction value of the object, the better, so that the operator (doctor) can see the bed surface better and make the operation process smoother!

Recently, PricewaterhouseCoopers released "hot trends in the medical industry in 2017", which forecasts the development prospects of China's medical and health industry from the perspectives of emerging technologies, payment means and changes in consumer demand. "11 emerging technologies will increasingly penetrate into people's daily medical care and daily life," said Xing Liping, partner of PricewaterhouseCoopers healthcare consulting services AI: the top one is artificial intelligence (AI). AI will be applied to medical insurance claims and fraud detection. This technology has been applied to some high-end medical insurance and national health insurance funds in China to reduce fraud and speed up claims processing. Big companies like Baidu have noticed that the real value of AI is not limited to this, but to enhanced diagnosis, genetic analysis and precision medicine. Telemedicine: telemedicine helps to reduce medical costs and save patients' time and energy. At present, dozens of Internet hospitals in China are the main drivers of telemedicine. Medical robots: medical robots are one of the weaker ones in China. The share of medical robots in European and American countries accounts for 62% and 24% respectively. It has been applied in at least four fields in China, including university, surgery and rehabilitation. VR: at present, the domestic application of virtual reality (VR) is to treat chronic diseases free of charge through necessary behavior changes. The Hong Kong Polytechnic University has developed and commercialized a virtual reality based rehabilitation training software to help patients with cognitive impairment improve their daily life and work skills. Doctor practice platform: doctors' online practice platform will be more in-depth for patients, such as "doctor almond". Through this platform, patients can establish long-term and stable contact with doctors they are familiar with and trust, and have sufficient time and opportunity to communicate with doctors. Accurate diagnosis: medical technology equipment will become more accurate and even have predictive ability. The increasing sensitivity of disease detection will reduce the occurrence of medical misdiagnosis. The focus is on the development of minimally invasive surgery and new compact devices, such as portable therapeutic ultrasound scanners, which are growing rapidly in the Chinese market. Sensors and Trackers: Although China currently has 980 million mobile phone users, accounting for the world's largest mobile medical market share, mobile applications and platforms have not attracted active users, let alone bring in much revenue, as they often provide more dispersed value. Some valuable areas include: predicting users' health needs and designing game based models to translate demand into medical action; providing the largest health consumer market (elderly and chronic patients) and one-stop service platform. Intelligent wearable devices, which can measure vital signs, respiratory rate, blood pressure, heart rate, electrocardiogram and body temperature, are gradually used by surgical patients in operating rooms and solitary users in remote areas. 3D equipment: in China and Asia, more and more patients demand customized orthopedic implants, prosthesis and orthodontic treatment. However, the application of 3D electrical and equipment spare parts for supplier manufacturing and hospital services is often ignored, and remote medical places may often have this demand. Next generation sequencing: This is an exciting area of research around the world, and it has been predicted that the technology will eventually be commercialized and the price will be reduced to $100. However, China has a reliable record in the speed and scale of technological optimization in the past. Companies such as BGI, Illumina and icarbonx are on this path. Internet of things: most medical technology companies are upgrading services that are independent but compatible with their products. The interaction between devices, data collection, value-added operations, and data feedback is the value of many other users. The importance of network security in this field is higher than that in other industries, because most of the health data leakage and hacker incidents occur at the Internet of things access point. Digital supply chain and blockchain: the integration of new data sources such as sensors and signal transmitters and medical machines provides opportunities for the development of China's health industry, not only improving safety and security, but also providing development opportunities in customization planning, procurement, production and delivery. Although the manufacturing industry is actively responding to the requirements of quality management system, blockchain solutions have great application potential in drug and food distribution and safety. "Traditional enterprises in the health industry should continue to seek cooperation with technology start-ups and ot

1、 We will deepen the reform of the examination and approval system for medical devices. 1. Encourage R & D innovation. Encourage clinical institutions and doctors to participate in the research and development of innovative medical devices. Priority shall be given to the examination and approval of innovative medical devices with product core technology invention patents and significant clinical value, as well as medical devices that are urgently needed in clinical practice and listed in the national key R & D plan and major scientific and technological projects. 2. The review and approval mechanism was improved. Improve the quality control system of evaluation. Establish a drug and medical device evaluation mechanism with clinical as the core, improve the system of indication team review, project manager, technical dispute resolution, communication and exchange, priority review, review information disclosure, etc., and gradually form a drug and medical device efficacy and safety guarantee system with technical review as the core, on-site inspection and product inspection as the support. 3. We will accelerate the reform of classified management of medical devices. Set up 16 professional groups of medical device classification technology, optimize and adjust the framework and structure of classification catalog, and issue the new version of medical device classification catalogue; research and develop 22 medical device nomenclature guidelines according to professional field setting, and gradually implement naming according to the common name of medical device; formulate coding rules of medical device and construct coding system of medical device. The database of medical device classification, naming and coding was established. 2、 We will improve the system of regulations and standards. We have basically completed the formulation and revision of supporting regulations for medical devices, accelerated the research and transformation of international standards for medical devices, given priority to improving the basic general standards and high-risk product standards for medical devices, revised the guiding principles for technical review of medical device registration, and formulated technical guidelines for the production, operation, use and adverse event monitoring of medical devices. "Medical device standard improvement action plan" includes: 1. 500 medical device standards were formulated and revised, including 80 diagnostic reagent standards, 200 active medical device standards, 220 passive medical device standards and other standards; 2. 200 guiding principles for technical review and clinical trials of medical devices were formulated and revised. 150 kinds of reference materials for in vitro diagnostic reagents were developed; 3. To establish and improve the standardized management system of medical devices, relying on the existing resources, strengthen the construction of the national medical device standard management center, and provide standard management personnel to meet the needs. 3、 Strengthen the whole process supervision. 1. We should fully implement the quality management standards for clinical trials of medical devices, strengthen the supervision and inspection of clinical trials, and crack down on the falsification of clinical data; 2. We should fully implement the quality management standard of medical device production, and strengthen the production supervision of sterile and implantable medical devices; 3. We should fully implement the quality management standards for medical devices, strengthen the quality supervision of cold chain transportation and storage, and implement the online filing and verification system for purchasing and selling business personnel of production and operation enterprises; 4. Strictly implement the quality supervision and management measures for the use of medical devices, strictly control the quality of purchase, acceptance, storage, maintenance, deployment and use, and timely report the adverse events of medical devices. Strengthen the use management of implantable and other high-risk medical devices. 4、 Comprehensively strengthen on-site inspection and supervision sampling inspection. Focusing on the aspects of code of conduct, process compliance, data reliability, etc., we will carry out the whole project inspection of quality management for enterprises, severely crack down on various illegal behaviors such as fraud, and urge enterprises to strictly implement relevant quality management standards. Increase the frequency of registration inspection, flight inspection and overseas inspection, and improve the inspection ability. Strengthen the inspection of sterile and implantable medical devices and in vitro diagnostic reagents. The "enhanced medical device inspection" program includes: 1. The national level carries out a full project inspection for all the third class medical device manufacturers and the second class sterile medical device manufactu