1 Scope
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-Eintended 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-Eintended 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.

