{"id":517081,"date":"2024-11-05T14:43:56","date_gmt":"2024-11-05T14:43:56","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/can-csa-z8637-08\/"},"modified":"2024-11-05T14:43:56","modified_gmt":"2024-11-05T14:43:56","slug":"can-csa-z8637-08","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/csa\/can-csa-z8637-08\/","title":{"rendered":"CAN\/CSA-Z8637-08"},"content":{"rendered":"

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

This is the first edition of CAN\/CSA-Z8637, Cardiovascular implants and artificial organs – Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators, which is an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 8637 (second edition, 2004-10-01). It replaces the previous edition published in 1994 as CAN\/CSA-Z364.1.1, Haemodialysers, Haemofilters and Haemoconcentrators (adopted ISO 8637:1989). At the time of publication, ISO 8637:2004 is available from ISO in English only. CSA will publish the French version when it becomes available from ISO.<\/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 for humans.<\/p>\n

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