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Updated: Feb 9, 2026

High-throughput Identification of Bacteria Repellent Polymers for Medical Devices
Published on: November 5, 2016
[Analysis of Common Problems in Classifcation of Medical Devices]
Jinglong Tang1, Yue Wang1, Hong Xu1
1National Institutes for Food and Drug Control, Beijing, 100050.
Objectives:
The present study was designed to analysis some misunderstanding on "medical devices classification rules" of CFDA, in order to correct understand and use the regulation.
Methods:
The contents of "medical devices classification rules" by CFDA have been analysis and generalized.
Results:
Through analyzing, we can conclude as followed:the priority principle of classification catalogue; the comprehensive judgment principle based on the classification decision table and special classification principles; medical devices' management class could be changed by CFDA according to risk analysis results.
Conclusions:
It is helpful to reach an agreement on the classification of a medical device among the regulatory authorities, production enterprises and other aspects, and establish a solid foundation for CFDA's regulatory science.
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