YY/T 1842.1-2022 Medical devices-connectors for reservoir delivery systems for healthcare applications-part 1: general requirements and common test methods

Standard Number: YY/T 1842.1-2022(YY/T1842.1-2022)
Chinese:医疗器械 医用贮液容器输送系统用连接件 第1部分:通用要求和通用试验方法
English:Medical devices-connectors for reservoir delivery systems for healthcare applications-part 1: general requirements and common test methods

Effective Date:2023-06-01
ICS:11.040.25
Standard Applicability:This document specifies general requirements for connectors for reservoir container delivery systems in medical applications. These reservoir connections are used in medical devices or accessories intended for use on patients. This document also specifies the medical fields in which these receptacle connectors are intended to be used. These medical fields include, but are not limited to, the following applications: respiratory; gastrointestinal; neurological; intravascular; citrate anticoagulant, and irrigation. Unless otherwise specified in the YY/T 1842 series, the receptacle connections specified herein are non-interconnecting with the following: receptacle connections for all other applications specified in the YY/T 1842 series; removable temperature sensor ports as specified in Appendix EE of ISO 80601-2-74:2017; and threaded connections as specified in Appendix B of ISO 17256. The application part of the YY/T 1842 series may specify other connections that are not interconnected with the receptacle connections (specified in the application part). This document specifies the methodology for evaluating the non-interconnecting characteristics of liquid receptacle connections based on their inherent design and dimensions. This document does not specify requirements for medical devices or accessories using these reservoir vessel connectors, which are given in the relevant standards for the particular medical device or accessory. This document also specifies test methods for verifying the generic performance requirements of the receptacle connections. The performance requirements for these generic test methods are specified in the application section and not in the generic section.

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