Medical device supervision has always been a problem. In particular, the supervision of imported medical devices is more difficult. China's medical device level lags far behind that of developed countries. The supervision team has very limited understanding of medical devices only. Under such circumstances, Doing a good job of supervision is not an easy task. The lack of supervision has caused the safety of imported medical devices to be solved, which has brought more hidden dangers to the safety of the people. We urgently need relevant departments to find suitable regulatory measures to enable imported medical devices to better serve the people.
China's medical device market is expanding, and the demand for medical devices is growing rapidly. China's medical device development period is far behind the developed countries. Many products must rely on imports. In recent years, the amount and quantity of imported medical devices have been Maintaining sustained growth, especially for high-end medical devices, its position in the Chinese market is irreplaceable due to its high-end and advanced nature. As the public's health requirements increase, such products become an essential health-assisting product for medical institutions and the public. .
Contrary to the high quality of medical devices, China's relevant regulatory level is seriously lagging behind. Even for the supervision of local medical devices, there are many problems, and it is even more difficult to regulate imported medical devices. Supervision in all walks of life is a problem, and medical equipment as a high-tech industry has high barriers. This industry involves many disciplines and is a product of high-level integration of multiple technologies. Cooperating with relevant experts and researchers, there is no way to start with certain medical devices. It is not incomprehensible for supervisors to look up the subject of supervision.
There are many special features in the use of medical devices. For example, some medical devices are used in medical institutions, and other methods are used in civilian use. Some medical devices are the same in medical civilians. Medical device products are diverse, and the efficacy and use of each type of product are very different. In particular, the specifications of imported medical devices are becoming more and more concise, and professionals do not know much about them. Regulators are even less able to start. How to manage imported medical equipment is a difficult problem facing the industry at present. Relevant departments should also seek solutions according to the actual situation of the market. Otherwise, it will not be able to do a good job in supervising people's lives and safety. We also look forward to the early resolution of this problem, which is also a means to promote the quality of imported products and ensure the healthy development of the industry.
Feline Infectious Peritonitis (FIP), referred to as Feline Infectious Peritonitis (FIP), is a fatal abnormal immune response that occurs in cats. It is caused by the mutation of the feline coronavirus carried by cats. As a high-incidence and fatal disease of pet cats, the current incidence of feline abdominal transmission is about 10%.
The symptoms of cats are usually divided into two categories, namely wet FIP and dry FIP, of which wet FIP accounts for the majority of all cases. About 70%, manifested as abdominal pleural effusion, abnormal bulging; dry FIP cats have different symptoms, depending on the type of organ affected by the virus.
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