Back

EVS-EN ISO 8872:2004

Aluminium caps for transfusion, infusion and injection bottles - General requirements and test methods

General information
Withdrawn from 01.12.2022
Base Documents
ISO 8872:2003; EN ISO 8872:2003
ICS Groups
11.040.20 Transfusion, infusion and injection equipment
Directives or regulations
None

Standard history

Status
Date
Type
Name
01.12.2022
Main
EVS-EN ISO 8872:2022
10.12.2004
Main
EVS-EN ISO 8872:2004
Main
EVS-EN 28872:1999
This International Standard specifies general requirements and test methods for aluminium caps for injection vials, and for infusion and transfusion bottles.
*
*
*
PDF
12.20 € incl tax
Paper
12.20 € incl tax
Browse standard from 2.44 € incl tax
Standard monitoring
English

Related products

Main

EVS-EN ISO 8872:2022

Aluminium caps and aluminium/plastic caps for infusion bottles and injection vials - General requirements and test methods (ISO 8872:2022)
Newest version Valid from 01.12.2022
Main

EVS-EN ISO 80369-1:2018

Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2018)
Newest version Valid from 03.12.2018
Main

EVS-EN 60601-2-24:2015

Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers
Newest version Valid from 08.06.2015
Main

EVS-EN 60601-2-40:2019

Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Newest version Valid from 16.01.2019

Customers who bought this item also bought

Main

EVS-EN ISO 14405-1:2010

Geometrical product specifications (GPS) - Dimensional tolerancing - Part 1: Linear sizes (ISO 14405-1:2010)
Withdrawn from 04.10.2016
Main

EVS-EN ISO 14405-2:2011

Geometrical product specifications (GPS) - Dimensional tolerancing - Part 2: Dimensions other than linear sizes (ISO 14405-2:2011)
Withdrawn from 01.02.2019
Amendment

EVS-EN ISO 8871-2:2004/A1:2014

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - Amendment 1 (ISO 8871-2:2003/Amd 1:2005)
Withdrawn from 15.06.2020
Main

EVS-EN ISO 8871-5:2014

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2005)
Withdrawn from 06.12.2016

Standards designation

EVS Estonian standard
EN European standard (published by an CEN or CENELEC)
EN ISO International standard adopted as an European standard
ISO International Organization for Standardization’s standard
IEC International Electrotechnical Commission’s standard
HD CENELEC’s harmonisation document
   
EVS-EN European standard implemented in Estonia
EVS-EN ISO International standard adopted in Europe and implemented in Estonia
EVS-EN ISO/IEC International standard/International electrotechnical standard adopted in Europe and implemented in Estonia
EVS-IEC International electrotechnical standard implemented in Estonia
EVS-ISO International standard implemented in Estonia
   
A, AMD amedment
+A a full standard plus the amendment
/A only amendment
COR, AC corrigendum
+COR a full standard plus the corrigendum
NA national annex
+NA a full standard plus the national annex
/NA only national annex
TS technical specification
TR technical report
CWA agreement, developed by a CEN or CENELEC
prEVS-EN (etc) draft standard
   
et the standard is in Estonian only
en the standard is in English only
et-en the standard is in Parallel text Estonian-English

Contact

standard@evs.ee
+372 605 5060
Akadeemia tee 21/6, Tallinn, 12618, Estonia
Reg. code 80120020
Eesti Standardimis- ja Akrediteerimiskeskus MTÜ
E-N 8:30-17:00 R 8:30-16:00

Assistance in ordering

Direct links

Mastercard
Visa
Paypal
Swedbank
SEB
Luminor
LHV
Copyright © 2024 EVS. All rights reserved.