Abstract
Ïã¸ÛÁùºÏ²Ê¿ª½± 7886-1:2017 specifies requirements and test methods for verifying the design of empty sterile single-use hypodermic syringes, with or without needle, made of plastic or other materials and intended for the aspiration and injection of fluids after filling by the end-users. This document does not provide requirements for lot release. The syringes are primarily for use in humans.
Sterile syringes specified in this document are intended for use immediately after filling and are not intended to contain the medicament for extended periods of time.
It excludes syringes for use with insulin (see Ïã¸ÛÁùºÏ²Ê¿ª½± 8537), single-use syringes made of glass, syringes for use with power-driven syringe pumps, syringes pre-filled by the manufacturer, and syringes intended to be stored after filling (e.g. in a kit for filling by a pharmacist).
Hypodermic syringes without a needle specified in this document are intended for use with hypodermic needles specified in Ïã¸ÛÁùºÏ²Ê¿ª½± 7864.
General information
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Status: PublishedPublication date: 2017-05
Corrected version (en): 2019-08
Corrected version (fr): 2019-08Stage: International Standard to be revised [90.92] -
Edition: 2Number of pages: 28
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Technical Committee :Ïã¸ÛÁùºÏ²Ê¿ª½±/TC 84ICS :11.040.25
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Life cycle
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Previously
WithdrawnÏã¸ÛÁùºÏ²Ê¿ª½± 7886-1:1993
WithdrawnÏã¸ÛÁùºÏ²Ê¿ª½± 7886-1:1993/Cor 1:1995
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Now
PublishedÏã¸ÛÁùºÏ²Ê¿ª½± 7886-1:2017
A standard is reviewed every 5 years
Stage: 90.92 (To be revised) -
Will be replaced by
Under developmentÏã¸ÛÁùºÏ²Ê¿ª½±/AWI 7886-1
Opening hours:
Monday to Friday - 09:00-12:00, 14:00-17:00 (UTC+1)