BS EN ISO 10555-6:2017+A1:2019 Intravascular Catheters: Sterile and Single-Use Catheters Subcutaneous Implanted Ports

Introducing the BS EN ISO 10555-6:2017+A1:2019, a comprehensive standard that sets the benchmark for intravascular catheters, specifically focusing on sterile and single-use catheters with subcutaneous implanted ports. This standard is an essential resource for healthcare professionals, manufacturers, and regulatory bodies involved in the design, production, and application of intravascular catheters.

Key Features and Benefits

This standard provides detailed guidelines and specifications to ensure the highest quality and safety of intravascular catheters. Here are some of the key features and benefits:

• Comprehensive Coverage: With 28 pages of in-depth information, this standard covers all aspects of intravascular catheters, ensuring that every detail is addressed.
• Up-to-Date Information: Released on November 5, 2019, this standard includes the latest amendments and updates, ensuring that you have access to the most current information available.
• International Recognition: As a part of the ISO 10555 series, this standard is recognized globally, making it a valuable resource for international compliance and standardization.
• Focus on Safety: The guidelines emphasize the importance of sterility and single-use applications, reducing the risk of infection and ensuring patient safety.

Who Should Use This Standard?

The BS EN ISO 10555-6:2017+A1:2019 is designed for a wide range of professionals and organizations, including:

• Healthcare Providers: Ensure that your medical practices align with the highest standards of patient care and safety.
• Manufacturers: Gain insights into the design and production requirements for intravascular catheters, ensuring compliance with international standards.
• Regulatory Bodies: Utilize this standard as a reference for evaluating and approving intravascular catheter products.
• Research and Development Teams: Leverage the detailed specifications to innovate and improve catheter technologies.

Technical Specifications

Here are the technical details of the BS EN ISO 10555-6:2017+A1:2019 standard:

Standard Number	BS EN ISO 10555-6:2017+A1:2019
Pages	28
Release Date	2019-11-05
ISBN	978 0 539 03811 8
Status	Standard

Why Choose BS EN ISO 10555-6:2017+A1:2019?

Choosing this standard means choosing quality, safety, and reliability. Here are some reasons why this standard is a must-have:

• Enhanced Patient Safety: By adhering to the guidelines, healthcare providers can significantly reduce the risk of complications associated with intravascular catheters.
• Regulatory Compliance: Stay ahead of regulatory requirements and ensure that your products meet international standards.
• Quality Assurance: Implementing this standard helps maintain high-quality production processes, leading to better product performance and reliability.
• Global Acceptance: As a recognized international standard, it facilitates easier market entry and acceptance across different regions.

Conclusion

The BS EN ISO 10555-6:2017+A1:2019 is an indispensable resource for anyone involved in the field of intravascular catheters. Its comprehensive guidelines ensure that products are safe, effective, and compliant with international standards. Whether you are a healthcare provider, manufacturer, or regulatory body, this standard provides the necessary framework to achieve excellence in the design and application of intravascular catheters.

Invest in the BS EN ISO 10555-6:2017+A1:2019 standard today and ensure that your practices and products meet the highest standards of quality and safety.

BS EN ISO 10555-6:2017+A1:2019

This standard BS EN ISO 10555-6:2017+A1:2019 Intravascular catheters. Sterile and single-use catheters is classified in these ICS categories:

• 11.040.25 Syringes, needles and catheters

This part of ISO 10555 specifies requirements, performance, and user safety issues related to subcutaneous implanted ports and catheters for intravascular long-term use supplied in sterile condition and intended for single use.

This part of ISO 10555 does not specify requirements, performance, and user safety issues related to non-coring needles.

NOTE Subcutaneous implanted ports are known to be used for indications other than intravascular such as intra-peritoneal, intra-thecal, intra-pleural, and epidural access.