EN ISO 11608-3:2022
Current
The latest, up-to-date edition.
Needle-based injection systems for medical use - Requirements and test methods - Part 3: Containers and integrated fluid paths (ISO 11608-3:2022, Corrected version 2023-01)
04-05-2022
This document specifies requirements and test methods for design verification of containers and integrated fluid paths used with Needle-Based Injection Systems (NISs) according to ISO11608-1.It is applicable to single and multi-dose containers either filled by the manufacturer (primary container closure) or by the end-user (reservoir) (e.g. cartridges, syringes) and fluid paths that are integrated with the NIS at the point of manufacture.This document is also applicable to prefilled syringes (see ISO11040-8) when used with a NIS (see also scope of ISO 11608-1:2022).This document is not applicable to the following products:— sterile hypodermic needles;— sterile hypodermic syringes;— sterile single-use syringes, with or without needle, for insulin;— containers that can be refilled multiple times;— containers intended for dental use;— catheters or infusion sets that are attached or assembled separately by the user.
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
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Status |
Current
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Standards | Relationship |
PN-EN ISO 11608-3:2022-11 | Identical |
NF EN ISO 11608-3:2022 | Identical |
ÖNORM EN ISO 11608-3:2022 10 15 | Identical |
UNI EN ISO 11608-3:2022 | Identical |
ÖNORM EN ISO 11608-3:2024 01 01 | Identical |
BS EN ISO 11608-3:2022 | Identical |
UNE-EN ISO 11608-3:2022 | Identical |
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