EN ISO 9187-1:2003/AC:2005
(Corrigendum)Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2000)
Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2000)
TC - Addition of an A-deviation
Infusionsgeräte zur medizinischen Verwendung - Teil 1: Ampullen für Injektionspräparate (ISO 9187-1:2000)
Matériel d'injection à usage médical - Partie 1: Ampoules pour produits injectables (ISO 9187-1:2000)
Oprema za injiciranje za uporabo v medicini - 1. del: Ampule za paranteralne farmacevtske oblike (ISO 9187-1:2000)
General Information
- Status
- Withdrawn
- Publication Date
- 01-Mar-2005
- Withdrawal Date
- 25-Mar-2008
- Technical Committee
- CEN/SS S02 - Transfusion equipment
- Drafting Committee
- CEN/SS S02 - Transfusion equipment
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 26-Mar-2008
- Completion Date
- 26-Mar-2008
Relations
- Effective Date
- 22-Dec-2008
- Effective Date
- 22-Dec-2008
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Frequently Asked Questions
EN ISO 9187-1:2003/AC:2005 is a corrigendum published by the European Committee for Standardization (CEN). Its full title is "Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2000)". This standard covers: TC - Addition of an A-deviation
TC - Addition of an A-deviation
EN ISO 9187-1:2003/AC:2005 is classified under the following ICS (International Classification for Standards) categories: 11.040.20 - Transfusion, infusion and injection equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN ISO 9187-1:2003/AC:2005 has the following relationships with other standards: It is inter standard links to EN ISO 9187-1:2008, EN ISO 9187-1:2003. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN ISO 9187-1:2003/AC:2005 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2000)Oprema za injiciranje za uporabo v medicini - 1. del: Ampule za paranteralne farmacevtske oblike (ISO 9187-1:2000)Matériel d'injection a usage médical - Partie 1: Ampoules pour produits injectables (ISO 9187-1:2000)Infusionsgeräte zur medizinischen Verwendung - Teil 1: Ampullen für Injektionspräparate (ISO 9187-1:2000)11.040.20Transfuzijska, infuzijska in injekcijska opremaTransfusion, infusion and injection equipmentICS:SIST EN ISO 9187-1:2003/AC:2005en,fr,deTa slovenski standard je istoveten z:EN ISO 9187-1:2003/AC:200501-junij-2005SIST EN ISO 9187-1:2003/AC:2005SLOVENSKI
STANDARD
EUROPEAN STANDARDNORME EUROPÉENNEEUROPÄISCHE NORMEN ISO 9187-1:2003/ACMarch 2005Mars 2005März 2005ICS 11.040.20English versionVersion FrançaiseDeutsche FassungInjection equipment for medical use - Part 1: Ampoules for injectables (ISO9187-1:2000)Matériel d'injection à usage médical - Partie1: Ampoules pour produits injectables (ISO9187-1:2000)Infusionsgeräte zur medizinischenVerwendung - Teil 1: Ampullen fürInjektionspräparate (ISO 9187-1:2000)This corrigendum becomes effective on 2 March 2005 for incorporation in the three official languageversions of the EN.Ce corrigendum prendra effet le 2 mars 2005 pour incorporation dans les trois versions linguistiquesofficielles de la EN.Die Berichtigung tritt am 2.März 2005 zur Einarbeitung in die drei offiziellen Sprachfassungen der ENin Kraft.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMITÉ EUROPÉEN DE NORMALISATIONEUROPÄISCHES KOMITEE FÜR NORMUNGManagement Centre: rue de Stassart, 36
B-1050 Brussels© 2005 CENAll rights of exploitation in any form and by any means reserved worldwide for CEN national Members.Tous droits d'exploitation sous quelque forme et de quelque manière que ce soit réservés dans le monde entier auxmembres nationaux du CEN.Alle Rechte der Verwertung, gleich in welcher Form und in welchem Verfahren, sind weltweit den nationalen Mitgliedernvon CEN vorbehalten.Ref. No.:EN ISO 9187-1:2003/AC:2005 D/E/F
The following A-deviation is to be added:
Annex A (informative) A-deviation
A-deviation: National deviation due to regulations, the alteration of which is for the time being outside the competence of CEN/CENELEC member:
NOTE: Where standards fall under EC Directives it is the view of the Commission of the European Communities (OJ No G 59, 9.3, 1982) that the effect of the decision of the Court of Justice in case 815/79 Cremonini/Vrankovitch (European Court Reports 1980, p.3583) is that compliance with A-deviations is no longer mandator
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