SFDA: Notification on Related Operating Procedures of Providing Manufacturers with Copies of Product Standard for the Registration of Domestic Class Ⅲ and Overseas Medical Devices |
Directive; Document No: ShiYaoJianXieHan[2005]42; Promulgation Date: 2005-07-05
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For details, please contact us via email (fdclaw@hi2000.com).
(Chinese Version) |
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