Your cart is currently empty!

ISO 11608:2022
ISO 11608:2022 Needle-based injection systems for medical use – Requirements and test methods – Part 4: Needle-based injection systems containing electronics
CDN $351.00
Description
This document specifies requirements and test methods for needle-based injection systems (NISs) containing electronics with or without software (NIS-Es).
The needle-based injection system containing electronics can be single use or reusable and can be operated with or without electrical/conductive connections to other devices. The system is intended to deliver medication to a patient by self-administration or by administration by one other operator (e.g. caregiver or health care provider).
This document applies to electronic accessories that are intended to be physically connected to a NIS or NIS-E according to the NIS/NIS-E intended use.
This document also applies to electronic accessories that are intended to have electrical/conductive connections to a NIS or NIS-E according to the NIS/NIS-E intended use.
This document does not specify requirements for software in programmable NIS-E.
NOTE      IEC 60601-1:2005+AMD1:2012+AMD2:2020, Clause 14 addresses software life cycle processes.
This document does not specify requirements for cybersecurity.
Edition
2
Published Date
2022-04-07
Status
PUBLISHED
Pages
63
Format 
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment

Abstract
This document specifies requirements and test methods for needle-based injection systems (NISs) containing electronics with or without software (NIS-Es).
The needle-based injection system containing electronics can be single use or reusable and can be operated with or without electrical/conductive connections to other devices. The system is intended to deliver medication to a patient by self-administration or by administration by one other operator (e.g. caregiver or health care provider).
This document applies to electronic accessories that are intended to be physically connected to a NIS or NIS-E according to the NIS/NIS-E intended use.
This document also applies to electronic accessories that are intended to have electrical/conductive connections to a NIS or NIS-E according to the NIS/NIS-E intended use.
This document does not specify requirements for software in programmable NIS-E.
NOTE      IEC 60601-1:2005+AMD1:2012+AMD2:2020, Clause 14 addresses software life cycle processes.
This document does not specify requirements for cybersecurity.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-
ISO 3749:2022 Glass syringes – Determination of extractable tungsten
0 out of 5CDN $115.00 Add to cart -
ISO 7885:2010 Dentistry – Sterile injection needles for single use
0 out of 5CDN $115.00 Add to cart -
ISO 10555:2024 Intravascular catheters – Sterile and single-use catheters – Part 8: Catheters for extracorporeal blood treatment
0 out of 5CDN $115.00 Add to cart -
ISO 6009:2016 Hypodermic needles for single use – Colour coding for identification
0 out of 5CDN $76.00 Add to cart