ISO 11608-3:2022

Needle-based injection systems for medical use — Requirements and test methods — Part 3: Containers and integrated fluid paths

Needle-based injection systems for medical use — Requirements and test methods — Part 3: Containers and integrated fluid paths

Digital Document2022 edition2022Purchase Options

Referenced standards

ISO 10555-1:2013ISO 10555-5:2013ISO 10993-11ISO 10993-17ISO 11040-4ISO 11040-5ISO 11040-6ISO 11040-8ISO 11607-1ISO 11608-1:2022ISO 13926-1ISO 13926-2ISO 13926-3ISO 21881ISO 7864:2016ISO 80369-7ISO 8872ISO 9626:2016
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ISO 11608-3:2022

Needle-based injection systems for medical use — Requirements and test methods — Part 3: Containers and integrated fluid paths

Needle-based injection systems for medical use — Requirements and test methods — Part 3: Containers and integrated fluid paths

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 ISO?11608-1.

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 ISO?11040-8) 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.

Edition2022
Standard Part No3
Published Date2022
Published ByInternational Standardization Organisation
Page Count27