BS EN ISO 19211:2025 - Anaesthetic and Respiratory Equipment

Introducing the BS EN ISO 19211:2025, a pivotal standard in the realm of anaesthetic and respiratory equipment. This comprehensive document is essential for professionals involved in oxygen therapy, providing critical guidelines for the use of fire-activated oxygen shut-off devices. Released on August 28, 2025, this standard is a must-have for ensuring safety and efficiency in medical environments.

Key Features

• Standard Number: BS EN ISO 19211:2025
• Pages: 24
• ISBN: 978 0 539 35370 9
• Status: Standard

Overview

The BS EN ISO 19211:2025 standard is meticulously crafted to address the critical need for safety in oxygen therapy. It focuses on fire-activated oxygen shut-off devices, which are crucial in preventing potential hazards associated with oxygen use. This standard provides a detailed framework for the design, implementation, and maintenance of these devices, ensuring they function effectively in emergency situations.

Why This Standard is Essential

Oxygen therapy is a vital component of medical treatment for patients with respiratory issues. However, the presence of oxygen increases the risk of fire, making it imperative to have reliable safety mechanisms in place. The BS EN ISO 19211:2025 standard addresses this need by setting forth guidelines for fire-activated oxygen shut-off devices. These devices are designed to automatically stop the flow of oxygen in the event of a fire, thereby minimizing the risk of exacerbating the situation.

Comprehensive Guidance

With 24 pages of in-depth information, this standard provides comprehensive guidance on the following aspects:

• Design specifications for fire-activated oxygen shut-off devices
• Installation procedures to ensure optimal functionality
• Maintenance protocols to guarantee long-term reliability
• Testing methods to verify device performance

Who Should Use This Standard?

This standard is indispensable for a wide range of professionals, including:

• Medical equipment manufacturers
• Healthcare facility managers
• Safety officers in medical settings
• Regulatory compliance specialists

Benefits of Compliance

Adhering to the BS EN ISO 19211:2025 standard offers numerous benefits, such as:

• Enhanced safety for patients and healthcare providers
• Reduced risk of fire-related incidents during oxygen therapy
• Increased confidence in the reliability of oxygen therapy equipment
• Alignment with international safety standards

Conclusion

The BS EN ISO 19211:2025 standard is an essential resource for anyone involved in the provision of oxygen therapy. By setting clear guidelines for fire-activated oxygen shut-off devices, it plays a crucial role in enhancing safety and ensuring the effective delivery of care. Whether you are a manufacturer, healthcare provider, or safety officer, this standard is a valuable tool in your efforts to maintain the highest standards of safety and quality in medical environments.

BS EN ISO 19211:2025

This standard BS EN ISO 19211:2025 Anaesthetic and respiratory equipment. Fire-activated oxygen shut-off devices for use during oxygen therapy is classified in these ICS categories:

• 11.040.10 Anaesthetic, respiratory and reanimation equipment

This document specifies requirements for fire activated oxygen shut-off devices that stop the flow of oxygen in respiratory therapy tubing when activated by fire. NOTE 1        Typical arrangements for fire activated oxygen shut-off devices are shown in Annex C. NOTE 2        Respiratory therapy tubing is covered by ISO 17256. NOTE 3        Use of fire activated oxygen shut-off devices in medical devices or accessories is not mandated in this document. The fire activated oxygen shut-off devices specified in this document are not suitable for use with oxygen therapy systems with flows in excess of 20 l/min). NOTE 4        There is rationale for this clause in A.2. The requirements in this device-specific standard take precedence over any conflicting requirements in the general standard for airway devices (ISO 18190). All the common requirements that appear in the general standard for airway devices have been removed from this document.