ÍST EN ISO 23908:2013

Staða:

Fellur úr gildi - 5.10.2025

Íslenskt heiti:

Varnir gegn meiðslum af völdum beittra og oddhvassra áhalda - Kröfur og prófunaraðferðir – Stungu- og skurðvarnir fyrir einnota sprautur, æðaleggi, leiðara fyrir æðaleggi og nálar til notkunar við töku blóðsýna

Enskt heiti:

Sharps injury protection - Requirements and test methods - Sharps protection features for single-used hypodermic needles, catheters, introducers for catheters and needles used for blood sampling

Tengdur staðall:

ISO/DIS 23908-1:2009

Tækninefnd:

CEN/TC 205

ICS flokkur:

11.040

Auglýst:

30.9.2025

Umfang (scope):

Varnir gegn meiðslum af völdum beittra og oddhvassra áhalda - Kröfur og prófunaraðferðir – Stungu- og skurðvarnir fyrir einnota sprautur, æðaleggi, leiðara fyrir æðaleggi og nálar til notkunar við töku blóðsýna

Hafðu samband í síma 520-7150 varðandi þennan staðal.

Mynd sem fylgir ÍST EN ISO 23908:2025

ÍST EN ISO 23908:2025

This document provides requirements and test methods to evaluate the performance and usability of sharps injury protection mechanisms (SIPMs) of devices including a single use sharp, for administration and/or extraction of blood or body fluids and/or medicinal substances. The sharps injury protection mechanisms covered by this document can be provided integral to the device or for assembly with the device prior to use. The aim of the tests is to confirm minimization of risks of accidental sharps injury from contaminated sharps, after the period of intended use, including the path to safe disposal or recovery, where this is a legal requirement or the manufacturers’ decision. This document does not cover —     devices for medication loading and transfer, utilizing a blunt tip design, or —     invasive products whose intended use is to access small spaces, particularly ear, nose and throat, to perform ophthalmic procedures because their SIPMs have been found to adversely affect the usabil
Verð: 8.211 kr.
Mynd sem fylgir ÍST EN ISO 23908:2025

ÍST EN ISO 23908:2025

This document provides requirements and test methods to evaluate the performance and usability of sharps injury protection mechanisms (SIPMs) of devices including a single use sharp, for administration and/or extraction of blood or body fluids and/or medicinal substances. The sharps injury protection mechanisms covered by this document can be provided integral to the device or for assembly with the device prior to use. The aim of the tests is to confirm minimization of risks of accidental sharps injury from contaminated sharps, after the period of intended use, including the path to safe disposal or recovery, where this is a legal requirement or the manufacturers’ decision. This document does not cover —     devices for medication loading and transfer, utilizing a blunt tip design, or —     invasive products whose intended use is to access small spaces, particularly ear, nose and throat, to perform ophthalmic procedures because their SIPMs have been found to adversely affect the usabil
Verð: 8.211 kr.
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