BS EN ISO 7886-2:2020 Sterile Hypodermic Syringes for Single Use

Syringes for Use with Power-Driven Syringe Pumps

Introducing the BS EN ISO 7886-2:2020, a comprehensive standard that sets the benchmark for sterile hypodermic syringes designed for single use, specifically tailored for use with power-driven syringe pumps. This standard is an essential resource for healthcare professionals, medical device manufacturers, and quality assurance teams who are committed to ensuring the highest levels of safety and efficacy in medical procedures.

Standard Number: BS EN ISO 7886-2:2020
Pages: 28
Released: 2024-05-08
ISBN: 978 0 539 01729 8
Status: Standard

Why Choose BS EN ISO 7886-2:2020?

The BS EN ISO 7886-2:2020 standard is meticulously crafted to address the specific requirements and challenges associated with the use of hypodermic syringes in conjunction with power-driven syringe pumps. This standard ensures that the syringes meet stringent safety and performance criteria, providing peace of mind to both healthcare providers and patients.

Key Features:

• Comprehensive Guidelines: The standard provides detailed guidelines on the design, materials, and performance of sterile hypodermic syringes, ensuring they are fit for purpose and safe for use.
• Quality Assurance: Adhering to this standard helps manufacturers maintain high-quality production processes, reducing the risk of defects and ensuring consistent product performance.
• Patient Safety: By following the BS EN ISO 7886-2:2020 standard, healthcare providers can minimize the risk of complications during medical procedures, enhancing patient safety and care outcomes.
• Compatibility: The standard ensures that syringes are compatible with a wide range of power-driven syringe pumps, offering flexibility and convenience in various medical settings.

Applications and Benefits

The BS EN ISO 7886-2:2020 standard is applicable in numerous medical environments, including hospitals, clinics, and research facilities. It is particularly beneficial for procedures that require precise and controlled administration of medications or fluids, such as in critical care, anesthesia, and oncology.

Enhanced Precision: The use of syringes compliant with this standard ensures accurate dosing and delivery, which is crucial in treatments where precision is paramount.

Streamlined Operations: By standardizing syringe specifications, healthcare facilities can streamline their operations, reducing the complexity of inventory management and ensuring that staff are familiar with the equipment in use.

Regulatory Compliance: Adopting the BS EN ISO 7886-2:2020 standard helps organizations meet regulatory requirements, facilitating smoother audits and inspections.

Commitment to Excellence

The development of the BS EN ISO 7886-2:2020 standard reflects a commitment to excellence in medical device manufacturing and healthcare delivery. By setting high standards for product quality and safety, this standard plays a crucial role in advancing medical technology and improving patient outcomes.

Global Recognition: As an internationally recognized standard, BS EN ISO 7886-2:2020 is trusted by healthcare professionals and organizations worldwide, underscoring its importance in the global medical community.

Future-Proofing: With its release in 2024, this standard incorporates the latest advancements in medical technology and practices, ensuring that it remains relevant and effective in the years to come.

Conclusion

The BS EN ISO 7886-2:2020 standard is an indispensable tool for anyone involved in the design, manufacture, or use of sterile hypodermic syringes with power-driven syringe pumps. By adhering to this standard, you are not only ensuring compliance with international best practices but also contributing to the safety and well-being of patients worldwide.

Invest in the BS EN ISO 7886-2:2020 standard today and take a significant step towards enhancing the quality and safety of medical procedures in your organization.

BS EN ISO 7886-2:2020

This standard BS EN ISO 7886-2:2020 Sterile hypodermic syringes for single use is classified in these ICS categories:

• 11.040.25 Syringes, needles and catheters

This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps.

This document does not apply to syringes with auto-disable syringe features ( ISO 7886-3^{[ 2]}), syringes for use with insulin ( ISO 8537^{[ 3]}), single-use syringes made of glass, syringes prefilled with the injection by the manufacturer and syringes supplied with the injection as a kit for filling by a pharmacist. It does not address compatibility with injection fluids.