BS ISO 18193:2021+A1:2025 - Cardiovascular Implants and Artificial Organs: Cannulae for Extracorporeal Circulation

Introducing the BS ISO 18193:2021+A1:2025, a comprehensive standard that sets the benchmark for the design, production, and application of cannulae used in extracorporeal circulation. This essential document is a must-have for professionals in the field of cardiovascular implants and artificial organs, providing critical guidelines to ensure safety, efficacy, and quality in medical procedures.

Key Features and Benefits

• Standard Number: BS ISO 18193:2021+A1:2025
• Pages: 42
• Release Date: 30th July 2025
• ISBN: 978 0 539 33342 8
• Status: Standard

This standard is meticulously crafted to address the intricate requirements of cannulae used in extracorporeal circulation, a critical component in cardiovascular surgeries and treatments. With the latest amendments included, it reflects the most current advancements and best practices in the field.

Comprehensive Coverage

The BS ISO 18193:2021+A1:2025 spans 42 pages of detailed information, offering a thorough exploration of the specifications and requirements for cannulae. It covers a wide range of topics, including:

• Design specifications and material requirements
• Performance criteria and testing methods
• Safety and risk management protocols
• Quality assurance and control measures
• Guidelines for clinical application and usage

Each section is designed to provide clarity and guidance, ensuring that medical professionals and manufacturers can adhere to the highest standards of practice.

Why Choose BS ISO 18193:2021+A1:2025?

In the rapidly evolving field of cardiovascular medicine, staying updated with the latest standards is crucial. The BS ISO 18193:2021+A1:2025 offers several advantages:

• Enhanced Patient Safety: By adhering to this standard, healthcare providers can significantly reduce the risk of complications during extracorporeal procedures.
• Improved Clinical Outcomes: The guidelines help ensure that cannulae are used effectively, leading to better patient outcomes.
• Regulatory Compliance: This standard helps manufacturers and healthcare facilities meet regulatory requirements, facilitating smoother operations and approvals.
• Innovation and Development: By following the latest standards, manufacturers can innovate and develop new products that meet the highest quality benchmarks.

Who Should Use This Standard?

The BS ISO 18193:2021+A1:2025 is an invaluable resource for a wide range of professionals, including:

• Medical device manufacturers
• Healthcare providers and clinicians
• Regulatory bodies and compliance officers
• Research and development teams in medical technology
• Quality assurance and control specialists

By integrating this standard into their practices, these professionals can ensure that they are at the forefront of medical technology and patient care.

Stay Ahead with the Latest Amendments

The inclusion of Amendment 1:2025 ensures that this standard is up-to-date with the latest technological advancements and industry practices. This amendment provides additional insights and refinements to the original 2021 standard, making it even more relevant and applicable to current medical practices.

Conclusion

The BS ISO 18193:2021+A1:2025 is more than just a standard; it is a vital tool for ensuring the highest levels of safety, quality, and performance in the use of cannulae for extracorporeal circulation. Whether you are a manufacturer, healthcare provider, or regulatory professional, this document is essential for staying compliant and competitive in the field of cardiovascular implants and artificial organs.

Equip yourself with the knowledge and guidelines provided by this standard to enhance your practice and contribute to the advancement of medical technology and patient care.

BS ISO 18193:2021+A1:2025

• 11.040.40 Implants for surgery, prosthetics and orthotics