Concentrates for haemodialysis and related therapies

This European Standard specifies requirements for dry and liquid concentrates to be diluted for use as dialysing fluids in haemodialysis or related therapies. It addresses chemical and microbiological quality and purity, handling and labelling of concentrates, the requirements for containers and the tests to monitor chemical and microbiological contents and quality of such concentrates.
This European standard does not address the final mixing and use of these concentrates or the treated water used in connection with haemodialysis and related therapies.
This European standard does not apply to dialysing fluid regeneration systems.

Konzentrate für die Hämodialyse und verwandte Therapien

Diese Europäische Norm legt Anforderungen für trockene und flüssige Konzentrate fest, die für die
Verdünnung zur Verwendung als Dialysierflüssigkeit in der Hämodialyse oder ähnlichen Therapien bestimmt
sind. Sie behandelt die chemische und mikrobiologische Qualität und Reinheit, die Handhabung und
Kennzeichnung der Konzentrate, die Anforderungen an Behälter und die Prüfungen zur chemischen und
mikrobiologischen Überwachung der Inhaltsstoffe sowie die Qualität solcher Konzentrate.
Diese Europäische Norm behandelt nicht die endgültige Mischung und die Anwendung dieser Konzentrate
oder das im Zusammenhang mit der Hämodialyse und ähnlichen Therapien verwendete aufbereitete Wasser.
Diese Europäische Norm gilt nicht für Systeme zur Regeneration von Dialysierflüssigkeiten.

Concentrés pour hémodialyse et thérapies associées

La présente Norme européenne fixe des exigences applicables aux concentrés en poudre et liquides à diluer pour
être utilisés comme liquides de dialyse pour l’hémodialyse ou les thérapeutiques voisines. Elle traite de la qualité et
de la pureté chimique et microbiologique, du stockage et de l’étiquetage des concentrés ainsi que des exigences
relatives aux cubitainers et des essais à effectuer pour contrôler la teneur et la qualité chimique et microbiologique
de ces concentrés.
La présente Norme européenne ne traite ni des mélanges finaux, ni de l’utilisation de ces concentrés, ni de l’eau
traitée utilisée pour l’hémodialyse et les thérapeutiques voisines.
Elle ne s’applique pas aux systèmes de régénération du liquide de dialyse.

Koncentrati za hemodializo in podobne terapije

General Information

Status
Withdrawn
Publication Date
09-Sep-2009
Withdrawal Date
04-Jan-2016
Technical Committee
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
05-Jan-2016
Due Date
28-Jan-2016
Completion Date
05-Jan-2016

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2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Koncentrati za hemodializo in podobne terapijeKonzentrate für die Hämodialyse und verwandte TherapienConcentrés pour hémodialyse et thérapies associéesConcentrates for haemodialysis and related therapies11.120.99Drugi standardi v zvezi s farmacijoOther standards related to pharmaceuticsICS:Ta slovenski standard je istoveten z:EN 13867:2002+A1:2009SIST EN 13867:2003+A1:2009en,fr,de01-oktober-2009SIST EN 13867:2003+A1:2009SLOVENSKI
STANDARD



SIST EN 13867:2003+A1:2009



EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM
EN 13867:2002+A1
June 2009 ICS 11.040.20; 11.120.99 Supersedes EN 13867:2002English Version
Concentrates for haemodialysis and related therapies
Concentrés pour hémodialyse et thérapies associées
Konzentrate für die Hämodialyse und verwandte TherapienThis European Standard was approved by CEN on 30 December 2001 and includes Amendment 1 approved by CEN on 16 May 2009.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN Management Centre or to any CEN member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre:
Avenue Marnix 17,
B-1000 Brussels © 2009 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 13867:2002+A1:2009: ESIST EN 13867:2003+A1:2009



EN 13867:2002+A1:2009 (E) 2 Contents Page Foreword .3Introduction .41Scope .52Normative references .53Terms and definitions .54Requirements .64.1Concentration limits .64.2Water quality .64.3pH range .64.4Chemical quality .64.5Manufacturing process (filtration) .64.6Containers .64.7Microbiological quality .75Labelling and documentation requirements .75.1General .75.2Information to be given on the concentrate container .75.3Information to be given on the shipping container, if any .85.4Information to be given in the accompanying documents .85.5Colour coding .86Test methods .86.1Water quality .86.2pH .96.3Manufacturing process (filtration) .96.4Containers .96.5Microbiological quality .96.6Sterility .9Annex A (informative)
Examples of analytical methods . 10Annex ZA (informative)
!!!!Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC "Medical Devices""""" . 11Annex ZB (informative)
A-deviations . 13Bibliography . 14 SIST EN 13867:2003+A1:2009



EN 13867:2002+A1:2009 (E) 3 Foreword This document (EN 13867:2002+A1:2009) has been prepared by Technical Committee CEN /TC 205, "Non-active medical devices", the secretariat of which is held by DIN. This European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by December 2009 and conflicting national standards shall be withdrawn at the latest by March 2010. This document includes Amendment 1, approved by CEN on 2009-05-16. This document supersedes EN 13867:2002. The start and finish of text introduced or altered by amendment is indicated in the text by tags ! ". This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive(s). For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this document. For A-deviations, see Annex ZB. Annexes A, ZA and ZB are for information only. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. SIST EN 13867:2003+A1:2009



EN 13867:2002+A1:2009 (E) 4 Introduction Dialysing fluids contain electrolytes in concentrations approaching that of the composition of normal extra-cellular body fluid. They can also contain non-electrolytes such as dextrose. Dialysing fluid quality plays a key role in the safety and biocompatibility of the dialysis treatment. Because of the large volumes employed, dialysing fluids are generally prepared by diluting concentrates with water of suitable quality. The manufacturer of concentrates should utilize raw materials and techniques to minimize microbial contamination (a low bioburden). The concentrates should be stored in conditions that assure the maintenance of this low level. During the dilution and use of these concentrates it is essential to take precautions to minimize any microbial contamination. The dialysing fluid is prepared from concentrates manufactured, packaged and labelled according to this standard, mixed with defined large proportions of water meeting national requirements on water for dialysis. Operation of water treatment equipment, selection and handling of concentrates after delivery to the hospital or clinic, and operation of the dialysis equipment are the responsibility of the dialysis facility. The properties of the final mixed dialysing fluids are not within the control of concentrate manufacturers. This standard does not address the important clinical and technical processes connected with the selection of concentrates and preparation of dialysing fluids. Dialysis professionals make choices about the various applications (e.g. haemodialysis, haemodiafiltration, haemofiltration) and it is essential they understand the corresponding risks and the requirements for safety of fluids used for each therapy. SIST EN 13867:2003+A1:2009



EN 13867:2002+A1:2009 (E) 5 1 Scope This European Standard specifies requirements for dry and liquid concentrates to be diluted for use as dialysing fluids in haemodialysis or related therapies. It addresses chemical and microbiological quality and purity, handling and labelling of concentrates, the requirements for containers and the tests to monitor chemical and microbiological contents and quality of such concentrates. This European standard does not address the final mixing and use of these concentrates or the treated water used in connection with haemodialysis and related therapies.
This European standard does not apply to dialysing fluid regeneration systems. 2 Normative references This European Standard incorporates by dated or undated reference, provisions from other publications. These normative references are cited at the appropriate places in the text and the publications are listed hereafter. For dated references, subsequent amendments to or revisions of any of these publications apply to this European Standard only when incorporated in it by amendment or revision. For undated references the latest edition of the publication referred to applies (including amendments). EN 556,
Sterilization of medical devices – Requirements for medical devices to be labelled “Sterile” EN 980, Graphical symbols for use in the labelling of medical devices EN 1174-1, Sterilization of medical devices – Estimation of the population of micro-organisms on product – Part 1: Requirements EN 1174-2, Sterilization of medical devices - Estimation of the population of micro-organisms on product – Part 2: Guidance EN 1174-3, Sterilization of medical devices – Estimation of the population of micro-organisms on product – Part 3: Guide to the methods for validation of microbiological techniques European Pharmacopoeia 3rd edition: 1999 (including supplements 2000 and 2001)
3 Terms and definitions For the purpose of this European standard, the following terms and definitions apply: 3.1
acetate dialysing fluid dialysing fluid without bicarbonate, using acetate as a
...

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