9999js金沙老品牌(中国)有限公司-Macau Future Star

Service Item
Registration Renewal
Class II medical devices refer to those which have medium-risk, safety and effectiveness can be ensured by strict control. Domestic manufacturers need to register their products in provincial or municipal FDA according to applicant area. Overseas manufacturers should designate a Chinese agent to register in NMPA. Class III refers to higher-risk medical device and its safety and effectiveness can be ensured by taking special measures to strictly control. Both foreign and domestic manufacturers need to register their products in NMPA.

二三类延续注册.jpg

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