医疗器械CE认证流程

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医疗器械CE认证流程

CREATE TIME:2018-06-29 11:34BROWSE TIMES:1618

“CE”标志是一种产品安全认证标志，被视为制造商打开并进入欧洲市场的通行证。在欧盟市场“CE”标志属强制性认证标志，不论是欧盟内部企业生产的医疗器械，还是其他国家生产的医疗器械，如果要在欧盟市场上自由流通，就必须加贴“CE”标志，以表明医疗器械分别符合欧盟《有源植入医疗器械指令》、《医疗器械指令》、《体外诊断器械指令》的基本要求。

标签：医疗器械第三方注册服务

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