STN EN ISO 23500-4
Označenie: | STN EN ISO 23500-4 |
Platnosť: | Zrušená |
Počet strán: | 34 |
Jazyk: |
EN
|
Listinná verzia: | 17,20€ |
Elektronická verzia: |
a) Bez možnosti tlače, prenosu textu a obrázkov:
15,48€ b) Bez možnosti tlače, s prenosom textu a obrázkov: 17,20€ c) S možnosťou tlače, prenosu textu a obrázkov: 22,36€ |
Slovenský názov: | Návod na prípravu a riadenie kvality tekutín pre hemodialýzu a súvisiace terapie. Časť 4: Koncentráty pre hemodialyzované aplikácie a súvisiace terapie (ISO 23500-4: 2019) |
Anglický názov: | Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019) |
Dátum vydania: | 01. 08. 2019 |
Dátum zrušenia: | 01. 09. 2024 |
ICS: | 11.040.40 |
Triediaci znak: | 85 6122 |
Úroveň zapracovania: | idt ISO 23500-4:2019, idt EN ISO 23500-4:2019 |
Vestník: | 07/19 |
Zmeny: | |
Nahradzujúce normy: | STN EN ISO 23500-4:2024-09 (85 6122) |
Nahradené normy: | STN EN ISO 13958:2016-04 (85 6215) |
Poznámka vo Vestníku: | |
Predmet normy: | This document specifies minimum requirements for concentrates used for haemodialysis and related therapies. This document is addressed to the manufacturer of such concentrates. In several instances in this document, the dialysis fluid is addressed, which is made by the end user, to help clarify the requirements for manufacturing concentrates. Because the manufacturer of the concentrate does not have control over the final dialysis fluid, any reference to dialysis fluid is for clarification and is not a requirement of the manufacturer. This document includes concentrates in both liquid and powder forms. It also includes additives, also called spikes, which are chemicals that can be added to the concentrate to supplement or increase the concentration of one or more of the existing ions in the concentrate and thus in the final dialysis fluid. This document also specifies requirements for equipment used to mix acid and bicarbonate powders into concentrate at the user's facility. |
Náhľad normy: | Náhľad normy (PDF) |