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EVS-EN ISO 7886-2:1999

Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps

General information

Withdrawn from 02.06.2020
Base Documents
ISO 7886-2:1996; EN ISO 7886-2:1997
ICS Groups
11.040.20 Transfusion, infusion and injection equipment
Directives or regulations
None

Standard history

Status
Date
Type
Name
02.06.2020
Main
EVS-EN ISO 7886-2:2020
01.01.2000
Main
EVS-EN ISO 7886-2:1999
Specifies requirements for sterile single-use hypodermic syringes of nominal capacity 5 ml and above, made of plastics materials and intended for use with power-driven syringe pumps. Does not apply to syringes for use with insulin, single-use syringes made of glass, syringes prefilled with the injection by the manufacturer and syringes supplied with the injection as a doctors kid.

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Standard monitoring
English (PDF 198 KB)

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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