BS EN ISO 7886-4:2019: Sterile Hypodermic Syringes for Single Use with Re-use Prevention Feature

Introducing the BS EN ISO 7886-4:2019, a comprehensive standard that sets the benchmark for sterile hypodermic syringes designed for single use, equipped with a re-use prevention feature. This standard is an essential resource for healthcare professionals, manufacturers, and regulatory bodies who prioritize safety and efficiency in medical practices.

Key Features and Benefits

The BS EN ISO 7886-4:2019 standard is meticulously crafted to ensure that hypodermic syringes meet the highest safety and quality standards. Here are some of the key features and benefits:

• Re-use Prevention Feature: This standard emphasizes the importance of syringes that are designed to prevent re-use, significantly reducing the risk of cross-contamination and infection. This feature is crucial in maintaining the integrity of medical procedures and ensuring patient safety.
• Sterility Assurance: The standard outlines stringent requirements for maintaining sterility, ensuring that each syringe is free from contaminants and safe for use in medical settings.
• Comprehensive Guidelines: With 20 pages of detailed instructions and specifications, this standard provides a thorough understanding of the requirements for manufacturing and using these syringes effectively.
• International Recognition: As part of the ISO standards, this document is recognized globally, facilitating international trade and ensuring consistency in medical practices across borders.

Technical Specifications

The BS EN ISO 7886-4:2019 standard is a vital document for anyone involved in the production or use of hypodermic syringes. Here are the technical specifications:

• Standard Number: BS EN ISO 7886-4:2019
• Pages: 20
• Release Date: 2019-05-15
• ISBN: 978 0 539 05025 7
• Status: Standard

Why Choose BS EN ISO 7886-4:2019?

Choosing the BS EN ISO 7886-4:2019 standard means opting for a document that is at the forefront of medical safety and innovation. Here’s why it stands out:

• Enhanced Patient Safety: By adhering to this standard, healthcare providers can ensure that they are using syringes that minimize the risk of infection and enhance patient safety.
• Regulatory Compliance: This standard helps manufacturers and healthcare facilities comply with international regulations, avoiding legal issues and ensuring smooth operations.
• Quality Assurance: The guidelines provided in this standard ensure that syringes are manufactured to the highest quality, providing peace of mind to both healthcare providers and patients.
• Cost-Effective: By preventing re-use, these syringes help reduce the costs associated with treating infections and other complications arising from contaminated medical equipment.

Applications

The BS EN ISO 7886-4:2019 standard is applicable in various medical settings, including:

• Hospitals and Clinics: Ensuring that all hypodermic syringes used in these settings meet the highest safety standards.
• Pharmaceutical Companies: Assisting in the development and production of syringes that comply with international safety standards.
• Regulatory Bodies: Providing a benchmark for evaluating the safety and efficacy of hypodermic syringes.
• Medical Device Manufacturers: Guiding the design and production of syringes that meet global safety requirements.

Conclusion

The BS EN ISO 7886-4:2019 standard is an indispensable resource for anyone involved in the healthcare industry. Its focus on safety, quality, and international compliance makes it a critical tool for ensuring the well-being of patients and the efficiency of medical practices. By choosing this standard, you are investing in a safer, more reliable future for healthcare.

Embrace the future of medical safety with the BS EN ISO 7886-4:2019 standard, and ensure that your practices are aligned with the highest international standards.

BS EN ISO 7886-4:2019

• 11.040.25 Syringes, needles and catheters

This document specifies requirements for sterile single-use hypodermic syringes made of plastic and rubber materials with or without needle, and intended for the aspiration of fluids or for the injection of fluids immediately after filling and of design such that the syringe can be rendered unusable after use.

This document is not applicable to syringes made of glass [specified in ISO 595 (withdrawn)], auto-disable syringes for fixed dose immunization (ISO 7886‑3) and syringes designed to be pre-filled. It does not address compatibility with injection fluids. Other standards can be applicable when syringes are used for any other intended purpose than those specified in this document.

NOTE Syringes designed to reduce the risk of needle-stick injuries can also comply with this document with regard to their re-use prevention properties, but it is stressed that anti-needle-stick properties of syringes are not in themselves addressed in this document.