Објављен
ISO 15674:2016 specifies requirements for sterile, single-use, extracorporeal hard-shell cardiotomy/venous reservoir systems and soft venous reservoir bags intended for use as a blood reservoir during cardiopulmonary bypass (CPB) surgery.
It applies only to the blood reservoir aspects for multifunctional systems which can have integral parts such as blood-gas exchangers (oxygenators), blood filters, defoamers, blood pumps, etc.
ПОВУЧЕН
ISO 15674:2009
ОБЈАВЉЕН
ISO 15674:2016
90.93
Одлука о потврђивању стандарда
2. 5. 2023.
ОБЈАВЉЕН
ISO 15674:2016/Amd 1:2020