According to Insofar as packaging is concerned, medical devices can be divided into active medical devices, passive medical devices, namely, aseptic and non-sterile devices, in vitro reagents; and their marking according to the outer packaging, inner packaging, and product marking will be part of the difference, but the overall should be in line with the latest "medical device specifications and labeling regulations" (Bureau of Decree No. 6) and its related standards. Basic requirements:
Package identification, labeling content should be used in Chinese, the use of Chinese should be consistent with the national common language and writing standards.
The label can be attached to other languages, but should be expressed in Chinese shall prevail, medical device labels in the text, symbols, tables, figures, graphics, etc. should be accurate, clear and standardized.
Should play a correct guide to the user to use, operation for the purpose of allowing users to clearly understand the product and its operational precautions, and not for the purpose of corporate publicity, exaggerated the effect of use, the use of sensitive words to mislead the user.