This European Standard specifies the requirements for a terminally-sterilized medical device to be designated 'STERILE'. NOTE: For the purpose of the EC Directives for medical devices (see Bibliography), designation of a medical device as 'STERILE' is only permissible when a validated sterilization process has been applied. Requirements for validation and routine control of processes for the sterilization of medical devices are specified in EN 550, EN 552, EN 554, EN ISO 14160 and EN ISO 14937.
DIN EN 556-1 Berichtigung 1-2006由德国标准化学会 DE-DIN 发布于 2006-12。
DIN EN 556-1 Berichtigung 1-2006 在中国标准分类中归属于: C47 公共医疗设备,在国际标准分类中归属于: 11.080.01 消毒和灭菌综合。
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