ISO 14708-3:2017 is applicable to active implantable medical devices intended for electrical stimulation of the central or peripheral nervous system. The tests that are specified in this document are type tests and are to be carried out on a sample of a device to assess device behavioural responses, and are not intended to be used for the routine testing of manufactured products.
EN ISO 14708-3:2022由欧洲标准化委员会 IX-CEN 发布于 2022-07-27,并于 2022-10-31 实施,于 2023-01-31 废止。
EN ISO 14708-3:2022在国际标准分类中归属于: 11.040.40 外科植入物、假体和矫形。
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