BS EN ISO 18777-2:2025 - Transportable Liquid Oxygen Systems for Medical Use

Introducing the BS EN ISO 18777-2:2025, a comprehensive standard that sets forth the particular requirements for portable units of transportable liquid oxygen systems designed for medical use. This standard is an essential resource for manufacturers, healthcare providers, and regulatory bodies involved in the design, production, and utilization of portable liquid oxygen systems.

Overview of the Standard

The BS EN ISO 18777-2:2025 is a meticulously crafted document that provides detailed guidelines and specifications to ensure the safety, reliability, and efficiency of portable liquid oxygen systems. Released on November 26, 2025, this standard is a critical update in the field of medical oxygen delivery systems, reflecting the latest technological advancements and safety protocols.

Key Features and Benefits

• Comprehensive Guidelines: The standard offers a thorough set of requirements that cover all aspects of portable liquid oxygen systems, ensuring they meet the highest safety and performance standards.
• Enhanced Safety: By adhering to the guidelines set out in this standard, manufacturers can significantly reduce the risk of accidents and malfunctions, thereby enhancing patient safety.
• Improved Efficiency: The standard promotes the development of more efficient oxygen delivery systems, which can lead to better patient outcomes and more effective use of resources.
• Global Relevance: As an ISO standard, it is recognized internationally, facilitating global trade and ensuring compatibility across different markets.

Technical Specifications

The BS EN ISO 18777-2:2025 is a 16-page document, identified by the ISBN 978 0 539 25049 7. It is classified as a standard, meaning it provides authoritative guidelines that are widely accepted and implemented across the industry.

Who Should Use This Standard?

This standard is indispensable for a variety of stakeholders in the healthcare and medical device industries, including:

• Manufacturers: Companies involved in the design and production of portable liquid oxygen systems will find this standard crucial for ensuring their products meet international safety and performance criteria.
• Healthcare Providers: Hospitals and clinics that utilize portable oxygen systems can rely on this standard to ensure they are using equipment that is safe and effective for patient care.
• Regulatory Bodies: Organizations responsible for the approval and regulation of medical devices will use this standard as a benchmark for evaluating the safety and efficacy of portable oxygen systems.

Why Choose BS EN ISO 18777-2:2025?

Choosing the BS EN ISO 18777-2:2025 standard means committing to the highest levels of safety and quality in the field of medical oxygen delivery. This standard not only helps in maintaining compliance with international regulations but also fosters innovation and improvement in product design and functionality.

By implementing the guidelines of this standard, manufacturers can enhance their reputation for quality and reliability, while healthcare providers can ensure they are delivering the best possible care to their patients. Moreover, regulatory bodies can streamline their evaluation processes, knowing that products adhering to this standard meet rigorous international criteria.

Conclusion

The BS EN ISO 18777-2:2025 is more than just a set of guidelines; it is a commitment to excellence in the field of medical oxygen systems. Whether you are a manufacturer, healthcare provider, or regulatory body, this standard is an invaluable tool for ensuring the safety, efficiency, and reliability of portable liquid oxygen systems.

Stay ahead in the rapidly evolving medical field by integrating the BS EN ISO 18777-2:2025 into your operations. Embrace the future of medical oxygen delivery with confidence and assurance, knowing you are backed by a standard that represents the pinnacle of industry expertise and innovation.

BS EN ISO 18777-2:2025

This standard BS EN ISO 18777-2:2025 Transportable liquid oxygen systems for medical use is classified in these ICS categories:

• 11.040.99 Other medical equipment
• 11.040.10 Anaesthetic, respiratory and reanimation equipment

This document specifies particular requirements for portable units which are part of a transportable liquid oxygen system and used to provide a controlled flow of oxygen for inhalation by the patient in the home-care environment. Portable units are intended to be used without professional supervision, carried by patients while moving around and during their off-site activities and refilled from a base unit via a transfilling device through the portable unit’s filling port connector. NOTE            Requirements that are common to both portable units and base units are specified in ISO 18777-1.