EN ISO 8536-3:2009/A1:2022
(Amendment)Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles - Amendment 1 (ISO 8536-3:2009/Amd 1:2022)
Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles - Amendment 1 (ISO 8536-3:2009/Amd 1:2022)
Infusionsgeräte zur medizinischen Verwendung - Teil 3: Aluminium-Bördelkappen für Infusionsflaschen - Änderung 1 (ISO 8536-3:2009/Amd 1:2022)
No scope available
Matériel de perfusion à usage médical - Partie 3: Capsules en aluminium pour flacons de perfusion - Amendement 1 (ISO 8536-3:2009/Amd 1:2022)
Infuzijska oprema za uporabo v medicini - 3. del: Aluminijeve zaporke za infuzijske steklenice - Dopolnilo A1 (ISO 8536-3:2009/Amd 1:2022)
General Information
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Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 8536-3:2009/A1:2022
01-november-2022
Infuzijska oprema za uporabo v medicini - 3. del: Aluminijeve zaporke za infuzijske
steklenice - Dopolnilo A1 (ISO 8536-3:2009/Amd 1:2022)
Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles -
Amendment 1 (ISO 8536-3:2009/Amd 1:2022)
Infusionsgeräte zur medizinischen Verwendung - Teil 3: Aluminium-Bördelkappen für
Infusionsflaschen - Änderung 1 (ISO 8536-3:2009/Amd 1:2022)
Matériel de perfusion à usage médical - Partie 3: Capsules en aluminium pour flacons de
perfusion - Amendement 1 (ISO 8536-3:2009/Amd 1:2022)
Ta slovenski standard je istoveten z: EN ISO 8536-3:2009/A1:2022
ICS:
11.040.20 Transfuzijska, infuzijska in Transfusion, infusion and
injekcijska oprema injection equipment
SIST EN ISO 8536-3:2009/A1:2022 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 8536-3:2009/A1:2022
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SIST EN ISO 8536-3:2009/A1:2022
EN ISO 8536-3:2009/A1
EUROPEAN STANDARD
NORME EUROPÉENNE
September 2022
EUROPÄISCHE NORM
ICS 11.040.20
English Version
Infusion equipment for medical use - Part 3: Aluminium
caps for infusion bottles - Amendment 1 (ISO 8536-
3:2009/Amd 1:2022)
Matériel de perfusion à usage médical - Partie 3: Infusionsgeräte zur medizinischen Verwendung - Teil
Capsules en aluminium pour flacons de perfusion - 3: Aluminium-Bördelkappen für Infusionsflaschen -
Amendement 1 (ISO 8536-3:2009/Amd 1:2022) Änderung 1 (ISO 8536-3:2009/Amd 1:2022)
This amendment A1 modifies the European Standard EN ISO 8536-3:2009; it was approved by CEN on 19 March 2022.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of
this amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.
This amendment 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-CENELEC Management Centre has the
same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2022 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8536-3:2009/A1:2022 E
worldwide for CEN national Members.
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SIST EN ISO 8536-3:2009/A1:2022
EN ISO 8536-3:2009/A1:2022 (E)
Contents Page
European foreword . 3
2
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SIST EN ISO 8536-3:2009/A1:2022
EN ISO 8536-3:2009/A1:2022 (E)
European foreword
This document (EN ISO 8536-3:2009/A1:2022) has been prepared by Technical Committee ISO/TC 76
"Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical
use" in collaboration with CCMC.
This Amendment to the European Standard EN ISO 8536-3:2009 shall be given the status of a national
standard, either by publication of an identical text or by endorsement, at the latest by March 2023, and
conflicting national standards shall be withdrawn at the latest by March 2023.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
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,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania,
...
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