BS EN ISO 10524-3:2019规定了带集成压力调节器的气瓶阀[定义见3.26，以下简称带集成压力调节器的阀门（VIPRs）]的设计、型式试验和标记要求，用于治疗、管理和维护过程中的医用气体，诊断评估和护理患者或用于驱动手术工具的气体。交叉引用:ISO 32ISO 11363-1ISO 15245-1ISO 5145ISO 14971ISO/TR 7470ISO 15001ISO 11117ISO 9170-1IEC 60601-1+A1:2012ISO 13341ISO 15996EN 837-1ISO 10297:2014/AMD 1:2017ISO 10297:2014EN 13544-2:2002ISO 11114-1ISO 7000IEC/TR 62366-2:2016JIS T 7101:2014ASTM G175: 2013CAN/CGSB 24.2-M86ISO 4135ISO 7396-1IEC 60529AS 4484:2016CGA C-9:1988SS 01 91ISO 10156ISO 11114-2IEC 62366-1:2015ISO 22435:2007EN 1089-3:2011购买本文件时可提供的所有当前修订版均包含在购买本文件中。

BS EN ISO 10524-3:2019 specifies design, type testing, and marking requirements for cylinder valves with integrated pressure regulators [as defined in 3.26 and referred to hereafter as valves with integrated pressure regulators (VIPRs)] intended for the administration of medical gases in the treatment, management, diagnostic evaluation and care of patients or for gases used for driving surgical tools.Cross References:ISO 32ISO 11363-1ISO 15245-1ISO 5145ISO 14971ISO/TR 7470ISO 15001ISO 11117ISO 9170-1IEC 60601-1+ A1:2012ISO 13341ISO 15996EN 837-1ISO 10297:2014/AMD 1:2017ISO 10297:2014EN 13544-2:2002ISO 11114-1ISO 7000IEC/TR 62366-2:2016JIS T 7101:2014ASTM G175:2013CAN/CGSB 24.2-M86ISO 4135ISO 7396-1IEC 60529AS 4484:2016CGA C-9:1988SS 01 91ISO 10156ISO 11114-2IEC 62366-1:2015ISO 22435:2007EN 1089-3:2011All current amendments available at time of purchase are included with the purchase of this document.