tag:blogger.com,1999:blog-1614638590617016598.post390109664995708958..comments2024-03-17T02:15:30.623-07:00Comments on Market China: The medical devices Market in ChinaMarketing to Chinahttp://www.blogger.com/profile/12901300209066484124noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-1614638590617016598.post-78843480924165249582018-10-28T23:46:56.838-07:002018-10-28T23:46:56.838-07:00Extensive focus on emerging countries such as Indi...Extensive focus on emerging countries such as India and China which are expected to grow at approximately 15% CAGR through 2023 in the field of <a href="https://www.occamsresearch.com/healthcare/medical-devices-market-research-reports" rel="nofollow"><b>Medical Device Market</b></a>.Anonymoushttps://www.blogger.com/profile/00019306007085794751noreply@blogger.comtag:blogger.com,1999:blog-1614638590617016598.post-34253913980800627542017-08-26T05:35:16.300-07:002017-08-26T05:35:16.300-07:00Medical devices are organized into three classes i...Medical devices are organized into three classes in China - Class I, II and III - depending on the level of risk<br />From the apparatus (determined by purpose, structural characteristics, whether in direct contact with<br />The body, methods and status of use) from bottom to top9<br />. The classifications are mainly used for risk<br />management; Consequently, different categories of medical devices are governed by different rules. For example:<br /> Category I medical devices are considered to have a low level of risk, including safety and efficacy<br />Can be provided by routine administration;<br /> Class II medical devices are considered to be of medium level of risk, for which additional control<br />Is necessary to ensure their safety and effectiveness;<br /> Class III medical devices have high levels of risk, where special measures<br />Apply strict control and administration in terms of safety and efficiency.<br />Pursuant to the Regulation respecting the supervision and administration of medical devices, (March<br />2014) 10, the CDFA has introduced the classification management of products for Class I medical devices before they can<br />Be distributed in China. For Class II and Class III medical devices, manufacturers require the approval of<br />The CFDA.<br />A medical device can be divided into four categories according to its structural characteristics<br />(Powered / active or unfed / passive) and if it touches the human body. These categories are<br />as following:<br /> Passive human body in contact with medical devices;<br /> Non-human passive medical device in contact with medical devices;<br /> Active human body in contact with medical devices;<br /> Non-human active body in contact with medical devices.Olivierhttps://www.blogger.com/profile/06286435246341640803noreply@blogger.comtag:blogger.com,1999:blog-1614638590617016598.post-88508646921873367222017-06-17T02:47:10.106-07:002017-06-17T02:47:10.106-07:00Market Services<a href="http://sharplinegraphics.com/market-research-translation-services-in-india/" rel="nofollow">Market Services</a>Unknownhttps://www.blogger.com/profile/08073306730558808769noreply@blogger.com