ISO 8637:2004Withdrawn

Cardiovascular implants and artificial organs — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

Implants cardiovasculaires et organes artificiels — Hémodialyseurs, hémodiafiltres, hémofiltres et hémoconcentrateurs

Abstract / scope

ISO 8637:2004 specifies requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, hereinafter collectively referred to as 'the device', for use for humans.

ISO 8637:2004 is not applicable to extracorporeal blood circuits, plasmafilters, haemoperfusion devices, vascular access devices, blood pumps, pressure monitors for the extracorporeal blood circuit, air detection devices, systems to prepare, maintain or monitor dialysate, systems used to perform haemofiltration or haemoconcentration, reprocessing procedures and equipment.

Requirements for the extracorporeal blood circuit for haemodialysers, haemodiafilters, and haemofilters are specified in ISO 8638.

Life cycle

Replaces

ISO 8637:1989WithdrawnHaemodialysers, haemofilters and haemoconcentratorsInternational Standard · Published 6 Jul 1989 · ISO/TC 150/SC 2

Replaced by

ISO 8637:2010WithdrawnCardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentratorsInternational Standard · Published 28 Jun 2010 · ISO/TC 150/SC 2