{"id":513746,"date":"2024-11-05T14:25:43","date_gmt":"2024-11-05T14:25:43","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/can-csa-iso-863712\/"},"modified":"2024-11-05T14:25:43","modified_gmt":"2024-11-05T14:25:43","slug":"can-csa-iso-863712","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/csa\/can-csa-iso-863712\/","title":{"rendered":"CAN\/CSA-ISO 8637:12"},"content":{"rendered":"

Preface<\/strong><\/p>\n

This is the first edition of CAN\/CSA-ISO 8637, Cardiovascular implants and extracorporeal systems – Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, which is an adoption, without modification, of the identically titled ISO (International Organization for Standardization) Standard 8637 (third edition, 2010-07-01).<\/p>\n

It replaces the previous edition published in 2008 as CAN\/CSA-Z8637, Cardiovascular implants and artificial organs – Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (adopted ISO 8637:2004). <\/p>\n

Scope<\/strong><\/p>\n

This International Standard specifies requirements for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, hereinafter collectively referred to as the device, for use in humans.<\/p>\n

This International Standard is not applicable to: <\/p>\n