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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.10 Anaesthetic, respiratory and reanimation equipment>BS EN ISO 9170-1:2020 Terminal units for medical gas pipeline systems Terminal units for use with compressed medical gases and vacuum
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BS EN ISO 9170-1:2020 Terminal units for medical gas pipeline systems Terminal units for use with compressed medical gases and vacuum

BS EN ISO 9170-1:2020

Terminal units for medical gas pipeline systems Terminal units for use with compressed medical gases and vacuum

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Standard number:BS EN ISO 9170-1:2020
Pages:34
Released:2024-06-04
ISBN:978 0 580 88401 6
Status:Standard

BS EN ISO 9170-1:2020: Terminal Units for Medical Gas Pipeline Systems

Introducing the BS EN ISO 9170-1:2020, a comprehensive standard that sets the benchmark for terminal units used in medical gas pipeline systems. This essential document is designed to ensure the highest level of safety, reliability, and efficiency in the delivery of compressed medical gases and vacuum, which are critical components in healthcare facilities worldwide.

Overview

The BS EN ISO 9170-1:2020 standard is a pivotal resource for professionals involved in the design, installation, and maintenance of medical gas pipeline systems. It provides detailed guidelines and specifications for terminal units, which are the crucial points of connection between the pipeline system and the medical equipment used by healthcare providers.

With a total of 34 pages, this standard offers a thorough exploration of the requirements and testing methods necessary to ensure that terminal units meet the stringent demands of medical environments. Released on June 4, 2024, this document reflects the latest advancements and best practices in the field, making it an indispensable tool for ensuring compliance and enhancing patient safety.

Key Features

  • Standard Number: BS EN ISO 9170-1:2020
  • Pages: 34
  • Release Date: 2024-06-04
  • ISBN: 978 0 580 88401 6
  • Status: Standard

Why Choose BS EN ISO 9170-1:2020?

The importance of reliable medical gas delivery systems cannot be overstated. In critical care settings, the precision and dependability of these systems can directly impact patient outcomes. The BS EN ISO 9170-1:2020 standard ensures that terminal units are designed and tested to meet the highest standards of performance and safety.

By adhering to this standard, healthcare facilities can minimize the risk of gas leaks, contamination, and other potential hazards associated with medical gas systems. This not only protects patients but also enhances the working environment for healthcare professionals, allowing them to focus on providing the best possible care.

Comprehensive Coverage

The BS EN ISO 9170-1:2020 standard covers a wide range of topics related to terminal units for medical gas pipeline systems, including:

  • Design and construction requirements
  • Performance criteria
  • Testing methods and procedures
  • Marking and labeling requirements
  • Installation and maintenance guidelines

Each section is meticulously detailed to provide clear and actionable guidance for professionals in the field. Whether you are an engineer, installer, or healthcare facility manager, this standard is an invaluable resource for ensuring that your medical gas systems are up to code and functioning optimally.

Global Relevance

The BS EN ISO 9170-1:2020 standard is recognized internationally, making it a critical document for facilities that operate on a global scale. By implementing this standard, organizations can ensure consistency and compatibility across different regions, facilitating smoother operations and enhancing the quality of care provided to patients worldwide.

Invest in Safety and Quality

Investing in the BS EN ISO 9170-1:2020 standard is an investment in the safety and quality of your healthcare facility. By following the guidelines set forth in this document, you can ensure that your medical gas pipeline systems are equipped with terminal units that meet the highest standards of performance and reliability.

Don't compromise on the safety and efficiency of your medical gas systems. Equip your facility with the knowledge and tools necessary to deliver exceptional care by adhering to the BS EN ISO 9170-1:2020 standard.

Conclusion

The BS EN ISO 9170-1:2020 standard is an essential resource for any healthcare facility that utilizes medical gas pipeline systems. With its comprehensive guidelines and specifications, this document ensures that terminal units are designed, tested, and maintained to the highest standards of safety and performance.

Stay ahead of the curve and ensure the safety and reliability of your medical gas systems by incorporating the BS EN ISO 9170-1:2020 standard into your operations. This investment in quality and safety will pay dividends in the form of enhanced patient care and improved operational efficiency.

DESCRIPTION

BS EN ISO 9170-1:2020


This standard BS EN ISO 9170-1:2020 Terminal units for medical gas pipeline systems is classified in these ICS categories:
  • 11.040.10 Anaesthetic, respiratory and reanimation equipment

This document is intended especially to ensure the gas-specific assembly, mechanical resistance, flow, leakage and pressure drop of terminal units and to prevent their interchange between different gases and services and applies to terminal units:

  1. intended for use in medical gas pipeline systems in accordance with ISO 7396‑1;

  2. used as pressure outlets on pressure regulators in accordance with ISO 10524‑1;

  3. used as pressure outlets on pressure regulators integrated with cylinder valves (VIPR) in accordance with ISO 10524‑3.

This document applies to terminal units for use with the following gases for administration to patients or for medical uses (A):

  • oxygen (A);

  • nitrous oxide (A);

  • medical air (A);

  • carbon dioxide (A);

  • oxygen/nitrous oxide mixture (A);

  • helium/oxygen mixtures (A);

  • oxygen 93 (A);

  • gases and gas mixtures classified as medical device (A);

  • gases delivered to medical devices or intended for medical purposes (A);

  • gases and gas mixtures for medicinal use not specified above (A).

This document applies to terminal units for use with the following gases (B):

  • air for driving surgical tools (B);

  • nitrogen for driving surgical tools (B).

This document applies to terminal units for use with vacuum systems (C).

NOTE The requirements of this document can be used as guidelines for terminal units for other gases. These other gases will be considered for inclusion in this document when they come into general use.

This document specifies requirements for terminal units for supply and disposal of nitrogen and air for driving surgical tools.

This document specifies requirements for probes intended to be connected to the gas-specific connection point.

This document does not specify the dimensions of probes or of the gas-specific connection points.

NOTE Regional or national standards specifying dimensions of probes and gas-specific connection points are given in the Bibliography.

Other connection systems in national use may be acceptable under this document. Dimensioning for such connections will be specified by their respective national standards.

This document does not specify the requirements for terminal units for anaesthetic gas scavenging systems (AGSS), which are specified in ISO 9170‑2.

This document is intended especially to ensure the gas-specific assembly, mechanical resistance, flow, leakage and pressure drop of terminal units and to prevent their interchange between different gases and services and applies to terminal units:

  1. intended for use in medical gas pipeline systems in accordance with ISO 7396‑1;

  2. used as pressure outlets on pressure regulators in accordance with ISO 10524‑1;

  3. used as pressure outlets on pressure regulators integrated with cylinder valves (VIPR) in accordance with ISO 10524‑3.

This document applies to terminal units for use with the following gases for administration to patients or for medical uses (A):

  • oxygen (A);

  • nitrous oxide (A);

  • medical air (A);

  • carbon dioxide (A);

  • oxygen/nitrous oxide mixture (A);

  • helium/oxygen mixtures (A);

  • oxygen 93 (A);

  • gases and gas mixtures classified as medical device (A);

  • gases delivered to medical devices or intended for medical purposes (A);

  • gases and gas mixtures for medicinal use not specified above (A).

This document applies to terminal units for use with the following gases (B):

  • air for driving surgical tools (B);

  • nitrogen for driving surgical tools (B).

This document applies to terminal units for use with vacuum systems (C).

NOTE The requirements of this document can be used as guidelines for terminal units for other gases. These other gases will be considered for inclusion in this document when they come into general use.

This document specifies requirements for terminal units for supply and disposal of nitrogen and air for driving surgical tools.

This document specifies requirements for probes intended to be connected to the gas-specific connection point.

This document does not specify the dimensions of probes or of the gas-specific connection points.

NOTE Regional or national standards specifying dimensions of probes and gas-specific connection points are given in the Bibliography.

Other connection systems in national use may be acceptable under this document. Dimensioning for such connections will be specified by their respective national standards.

This document does not specify the requirements for terminal units for anaesthetic gas scavenging systems (AGSS), which are specified in ISO 9170‑2.