Product Compliance
Test/Filing/Registration
In accordance with the requirements of Measures for the Management of Medical Equipment Standard, Medical Instrument Standard System Revision Work Management Specification, the National Medical Products Administration organized the medical device industry standard system revision project selecting and revising in 2022. The project solicit opinions and the public organization expert argumentation, and identified in the year 2022, in total 116 medical device industry standards revision plan projects, and revising are hereby published. During the publicity period, if you have any objection, please feedback to National Medical Products Administration.
Publicity time: 7 days from the date of publication by the National Medical Products Administration
E-mail: mdct@nmpa.gov.cn (Please mark "Feedback on the 2022 Industry Standard System Revision Project" as the subject of the email.)
Attachments:
2022 Mandatory industry standard system revision plan for medical devices
2022 Recommended industry standard system revision plan for medical devices
National Medical Products Administration
April 13, 2022
【Attachment】
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