Analysis on Re-classifcation Management Procedure of Medical Devices in the United States.
10.3969/j.issn.1671-7104.2019.02.012
- Author:
Yue WANG
1
;
Chunqing ZHANG
1
;
Jia ZHENG
1
;
Shifu GUO
1
;
Ruihong MU
1
;
Xinhua YU
1
Author Information
1. National Institute for Food and Drug Control, Beijing, 100050.
- Publication Type:Journal Article
- Keywords:
classification;
dynamic management;
medical device;
working procedure
- MeSH:
China;
Equipment Safety;
Equipment and Supplies;
United States;
United States Food and Drug Administration
- From:
Chinese Journal of Medical Instrumentation
2019;43(2):118-121
- CountryChina
- Language:Chinese
-
Abstract:
A detailed analysis on re-classification procedure of medical devices from Food and Drug Administration.The experience on classification procedures,the work-flow of risk reanalysis and regulatory categories reassessment of listed products,as well as launching a comprehensive evaluation and downgrading of listed high-risk products were explored in recent years.Based on the analysis on classification procedures and supervision of medical device products in the USA,and combined with the current situation of classification of medical devices in China,some suggestions were put forward on the current classification mode of medical devices so as to improve the quality and efficiency of classified management of medical devices in China.
