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ILNAS-EN ISO 7886-2:2020 Edition 05/2020
Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps (ISO 7886-2:2020)
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Abstract

This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps. This document does not apply to syringes with auto-disable syringe features (ISO 7886-3[2]), syringes for use with insulin (ISO 8537[3]), single-use syringes made of glass, syringes prefilled with the injection by the manufacturer and syringes supplied with the injection as a kit for filling by a pharmacist. It does not address compatibility with injection fluids.

Status

Standard - Active

Origin

Technical Committee :
CEN/TC 205 : Non-active medical devices

Implementation

start of the vote on the project    16/05/2019   date of ratification (dor)    27/04/2020
end of the vote on the project    09/08/2019   date of anouncement (doa)    31/08/2020
start of the vote on the final project    30/01/2020   date of publication (dop)    30/11/2020
end of the vote on the final project    26/03/2020   date of withdrawal (dow)    30/11/2020


Publication Official Journal
of the Grand-Duchy of Luxembourg
16/11/2020
Reference Mémorial A N° 903

Relations

Relations to older standards
ILNAS-EN ISO 7886-2:1997

Relations to international standards
ISO 7886-2 
ISO 7886-2:2020 

International Classification for Standards (ICS codes) :

11.040.25 : Syringes, needles and catheters

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