Class I medical device products belong to the filing system, there are district (county) Food and Drug Administration management.
Approval procedures: 1, in the Food and Drug Administration website to declare, 2, in accordance with the prompts of the material one by one, 3, with the official seal directly to the district (county) Food and Drug Administration Service Window (Government Comprehensive Office of the Hall submission, the Food and Drug Administration receptionist on-site review of the materials qualified on the spot to issue the "Class I Medical Device Record Voucher".