This document specifies requirements and test methods for plasmafilters, which are devices intended to separate plasma from blood in therapeutic plasmapheresis therapy. This document specifies the requirements for sterile, single-use plasmafilters, intended for use on humans, hereinafter collectively referred to as “the device”, for use in humans. This document does not apply to;

—     extracorporeal blood circuits;

—     haemodialysers, haemodiafilters, haemofilters and haemoconcentrators;

—     haemoperfusion devices;

—     vascular access devices;

—     blood pumps;

—     systems or equipment intended to perform plasma separation.

NOTE 1       Requirements for the extracorporeal blood circuit are specified in ISO 8637-2.

NOTE 2       Requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators are specified in ISO 8637-1.