BS EN ISO 21649:2023

Needle-free injection systems for medical use. Requirements and test methods

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Standard number:	BS EN ISO 21649:2023
Pages:	48
Released:	2023-02-10
ISBN:	978 0 539 18826 4
Status:	Standard

BS EN ISO 21649:2023 Needle-free Injection Systems for Medical Use - Requirements and Test Methods

Introducing the BS EN ISO 21649:2023, the latest standard for needle-free injection systems for medical use. This comprehensive guide sets the benchmark for the requirements and test methods of needle-free injection systems, ensuring the highest level of safety and efficiency in the medical field.

Released on 10th February 2023, this standard is the most up-to-date and relevant guide for professionals in the medical field. With a total of 48 pages, it provides a thorough and detailed overview of the requirements and test methods for needle-free injection systems.

Why Choose BS EN ISO 21649:2023?

The BS EN ISO 21649:2023 is a must-have for any medical professional or organization that values safety, efficiency, and compliance. This standard ensures that your needle-free injection systems meet the highest international standards, reducing the risk of complications and improving patient outcomes.

With its unique ISBN number 978 0 539 18826 4, this standard is easily identifiable and accessible for all medical professionals. It is a valuable resource that can significantly enhance the quality of your medical services.

What Does BS EN ISO 21649:2023 Cover?

The BS EN ISO 21649:2023 covers a wide range of topics related to needle-free injection systems. It provides detailed requirements for the design, manufacturing, and testing of these systems, ensuring that they are safe, effective, and reliable.

It also outlines the test methods for these systems, providing clear and concise instructions for conducting these tests. This ensures that your needle-free injection systems are always performing at their best, providing the highest level of care for your patients.

Who Should Use BS EN ISO 21649:2023?

The BS EN ISO 21649:2023 is suitable for a wide range of professionals in the medical field. Whether you are a medical device manufacturer, a healthcare provider, or a medical researcher, this standard can provide you with the guidance and information you need to ensure the safety and effectiveness of your needle-free injection systems.

How to Get BS EN ISO 21649:2023?

Getting your copy of the BS EN ISO 21649:2023 is easy and straightforward. Simply order it online and have it delivered to your doorstep. With its comprehensive coverage and easy-to-understand language, this standard is a valuable addition to any medical professional's library.

Conclusion

The BS EN ISO 21649:2023 is more than just a standard. It is a commitment to safety, efficiency, and excellence in the medical field. By adhering to this standard, you are not only ensuring the quality of your needle-free injection systems but also improving the health and well-being of your patients.

So don't wait. Get your copy of the BS EN ISO 21649:2023 today and take your medical services to the next level.

DESCRIPTION

BS EN ISO 21649:2023

This standard BS EN ISO 21649:2023 Needle-free injection systems for medical use. Requirements and test methods is classified in these ICS categories:

11.040.20 Transfusion, infusion and injection equipment

This document applies to safety and performance and testing requirements for single-use and multiple-use Needle-Free Injection Systems (NFISs) intended for human use in clinics and other medical settings and for personal use by patients. The dose chamber of the NFIS is often disposable and intended to be replaced after either a single use or a limited number of uses. It is sometimes separable from the injection mechanism and often termed a “cartridge”, “ ampoule”, “syringe”, “capsule” or “disc”. In contrast, the dose chamber can also incorporate a permanent internal chamber designed to last through the claimed life of the device, and an additional member or members which eliminate the risk of cross-contamination. Excluded from this document are drug delivery methods which: — involve penetration of a part of the device itself into or through skin or mucous membranes (such as needles, tines, micro-needles, implantable slow-release drug devices); — generate aerosols, droplets, powders or other formulations for inhalation, insufflation, intranasal or oral deposition (such as sprays, inhalers, misters); — deposit liquids, powders, or other substances on the surface of skin or mucosal surfaces for passive diffusion or ingestion into the body (such as transdermal patches, liquid drops); — apply sonic or electromagnetic energy (such as ultrasonic or iontophoretic devices); — infusion systems for adding or metering medication into or through systems of artificial tubes, catheters, and/or needles which themselves enter the body.

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