Industry knowledge
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Basic theory of X-ray machine
Ordinary X-ray machine is mainly composed of console, high-voltage generator, head, table and various mechanical devices. X-ray tube is placed in the head. The high-voltage generator and the head of the small X-ray machine are assembled together, which is called the combined head for its lightne...Read more -
What is the medical device recall?
Medical device recall refers to the behavior of medical device manufacturers to eliminate defects by warning, inspection, repair, re labeling, modifying and improving instructions, software upgrading, replacement, recovery, destruction and other means according to the prescribed ...Read more -
What is the classification of medical device recall?
Medical device recall is mainly classified according to the severity of medical device defects First class recall, the use of the medical device may or has caused serious health hazards. Secondary recall, the use of the medical device may or has caused temporary or reversible health hazards. Thre...Read more -
The latest development of global mainstream flat panel detectors
Canon recently released three Dr detectors at the ahra in Anaheim, California, in July. The lightweight cxdi-710c wireless digital detector and cxdi-810c wireless digital detector have many changes in design and function, including more fillets, tapered edges and built-in grooves for processing a...Read more -
What is the content of the administrative measures for medical device recall (for Trial Implementation)?
Medical device recall refers to the behavior of medical device manufacturers to eliminate defects by warning, inspection, repair, re labeling, modifying and improving instructions, software upgrading, replacement, recovery, destruction and other means according to the prescribed procedures for a ...Read more -
What kind of punishment will be imposed if the medical device fails to fulfill the recall obligation?
If a medical device manufacturer finds a defect in the medical device and fails to recall or refuses to recall the medical device, it shall be ordered to recall the medical device and be fined three times the value of the medical device to be recalled; If serious consequences are caused, the regi...Read more -
What are the requirements of medical device recall?
Medical device manufacturers shall establish and improve the medical device recall system in accordance with the administrative measures for medical device recall (Trial Implementation) issued by the Ministry of health and implemented on July 1, 2011 (Order No. 82 of the Ministry of Health), coll...Read more -
Announcement on active recall of large medical equipment in September 2019
Philips (China) Investment Co., Ltd. reported that due to the products involved, Philips identified a small number of s7-3t and s8-3t Due to the incorrect programming of TEE probe in the manufacturing process,Philips (China) Investment Co., Ltd. made the portable color ultrasound diagnosis system...Read more -
Siemens Medical after sales fined heavily in South Korea
In January this year, the Korea Fair Trade Commission determined that Siemens abused its market leading position and engaged in unfair business practices in the after-sales service and maintenance of CT and MR imaging equipment in Korean hospitals. Siemens plans to file an administrative lawsuit ...Read more -
Some people say Dr market can do 10 billion, do you believe it?
Dynamic Dr product line From the first dynamic Dr launched in 2009 by Shimadzu to the current mainstream manufacturers have launched dynamic Dr products. From sporadic dynamic Dr products exhibition at medical equipment exhibition to dynamic Dr, it is becoming popular in the exhibition, and even ...Read more -
The latest development of X-ray flat panel detector in the world
Canon recently pre released three Dr detectors at the ahra in Anaheim, California, in July. The portable cxdi-710c wireless digital detector and cxdi-810c wireless digital detector have many changes in design and function, including more rounded corners, tapered edges an...Read more -
Software vulnerability found in Philips cardiovascular imaging device
According to the security agency report cve-2018-14787, it is a privilege management issue. In Philips’s intellispace cardiovascular (iscv) products (iscv version 2. X or earlier and Xcelera version 4.1 or earlier), “attackers with upgrade rights (including authenticated users) can ac...Read more