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API TR 2583 : Measurement of Produced Water for Custody Transfer

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174

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API TR 2581: Wet Gas Sampling

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API TR 2581 Wet Gas Sampling : Errata 1

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API SPEC 16B Coiled Tubing, Snubbing and Wireline Well Intervention Equipment

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API SPEC 5CT: Casing and Tubing w/ Addendum 1

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API SPEC 5CT: Casing and Tubing Addendum 1

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API RP 1161: Hazardous Liquid Pipeline Operator Qualification (OQ) : Edition 6

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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

SKU: 2ba8a7b6928b Category:

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

Language Detail Icon

English

Format Secure Icon

Secure PDF

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.

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