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CAN/CSA-Z23500:12
Guidance for the preparation and quality management of fluids for haemodialysis and related therapies (Adopted ISO 23500:2011, first edition, 2011-05-15, with Canadian deviations)
SKU: 2421759
Published by CSA Group
Publication Year 2012
100 pages
Withdrawn
Product Details
As an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 23500, Z23500 functions as a recommended practice. With a focus on the user’s responsibilities, it provides dialysis practitioners with guidance on the preparation of dialysis fluid for haemodialysis and related therapies and substitution fluid for use in online therapies, such as haemodiafiltration and haemofiltration.
Preface
his is the first edition of CAN/CSA-Z23500, Guidance for the preparation and quality management of fluids for haemodialysis and related therapies, which is an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 23500 (first edition, 2011-05-15).
At the time of publication, ISO 23500:2011 is available from ISO in English only. CSA will publish the French version when it becomes available.
Scope
1.1 General
This International Standard provides dialysis practitioners with guidance on the preparation of dialysis fluid for haemodialysis and related therapies and substitution fluid for use in online therapies, such as haemodiafiltration and haemofiltration. As such, this International Standard functions as a recommended practice.
1.2 Inclusions
This International Standard addresses the user's responsibility for the dialysis fluid once the equipment used in its preparation has been delivered and installed. For the purposes of this International Standard, the dialysis fluid includes water used for the preparation of dialysis fluid and substitution fluid, water used for the preparation of concentrates at the user's facility, as well as concentrates and the final dialysis fluid and substitution fluid.
Included in the scope of this International Standard are
a) the quality management of equipment used to treat and distribute water used for the preparation of dialysis fluid and substitution fluid, from the point at which municipal water enters the dialysis facility to the point at which the final dialysis fluid enters the dialyser or the point at which substitution fluid is infused,
b)equipment used to prepare concentrate from powder or other highly concentrated media at a dialysis facility, and
c) preparation of the final dialysis fluid or substitution fluid from dialysis water and concentrates.
NOTE Because water used to prepare dialysis fluid is commonly prepared and distributed using the same equipment as the water used to reprocess dialysers, water used to reprocess dialysers is also covered by this International Standard.
1.3 Exclusions
Excluded from the scope of this International Standard are sorbent-based dialysis fluid regeneration systems that regenerate and recirculate small volumes of dialysis fluid, systems for continuous renal replacement therapy that use prepackaged solutions, and systems and solutions for peritoneal dialysis.
his is the first edition of CAN/CSA-Z23500, Guidance for the preparation and quality management of fluids for haemodialysis and related therapies, which is an adoption, with Canadian deviations, of the identically titled ISO (International Organization for Standardization) Standard 23500 (first edition, 2011-05-15).
At the time of publication, ISO 23500:2011 is available from ISO in English only. CSA will publish the French version when it becomes available.
Scope
1.1 General
This International Standard provides dialysis practitioners with guidance on the preparation of dialysis fluid for haemodialysis and related therapies and substitution fluid for use in online therapies, such as haemodiafiltration and haemofiltration. As such, this International Standard functions as a recommended practice.
1.2 Inclusions
This International Standard addresses the user's responsibility for the dialysis fluid once the equipment used in its preparation has been delivered and installed. For the purposes of this International Standard, the dialysis fluid includes water used for the preparation of dialysis fluid and substitution fluid, water used for the preparation of concentrates at the user's facility, as well as concentrates and the final dialysis fluid and substitution fluid.
Included in the scope of this International Standard are
a) the quality management of equipment used to treat and distribute water used for the preparation of dialysis fluid and substitution fluid, from the point at which municipal water enters the dialysis facility to the point at which the final dialysis fluid enters the dialyser or the point at which substitution fluid is infused,
b)equipment used to prepare concentrate from powder or other highly concentrated media at a dialysis facility, and
c) preparation of the final dialysis fluid or substitution fluid from dialysis water and concentrates.
NOTE Because water used to prepare dialysis fluid is commonly prepared and distributed using the same equipment as the water used to reprocess dialysers, water used to reprocess dialysers is also covered by this International Standard.
1.3 Exclusions
Excluded from the scope of this International Standard are sorbent-based dialysis fluid regeneration systems that regenerate and recirculate small volumes of dialysis fluid, systems for continuous renal replacement therapy that use prepackaged solutions, and systems and solutions for peritoneal dialysis.
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