兹证明上述医疗器械已准许在中国境内生产和销售。 This is to certify that the above medical device(s) have been approved for manufacture and sale in China. 出具出口销售证明作为服务事项提供给中国境内医疗器械注册人或者备案人。出具出口销售证明时,出具证明的部门未评估或者验证产品是否符合进口国家(地区)的要求,申请人有责任确保遵守进口国家(地区)的相关要求。 The Certificate for Exportation is issued as a service item to the Medical Device Registration Certificates or Filing Entities in China. The applicants are obligated to comply with the requirements of the importing countries(regions), as the certifying authority does not evaluate or verify if the products comply with the requirements of the importing countries(regions) when issuing the Certificate for Exportation. *如医疗器械注册证或者产品备案、医疗器械生产许可证或者生产备案被依法吊销、撤销、注销或者取消的,本证明自吊销、撤销、注销或者取消之日起失效。 *If the Medical Device Registration Certificate, Medical Device Filing Certificate/Filing Number Notification, or the Medical Device Manufacturing License/Filing Certificate is revoked, withdrawn, de-registered or canceled according to law, this Certificate for Exportation shall become invalid from the date of such revocation, withdrawal, de-registration or cancellation. |