NEN-EN-ISO 21649:2003 Ontw. en

Needle-free injectors for medical use - Requirements and test methods

  • This norm is withdrawn since 15-06-2006

29,64 35,86 Incl BTW

About norm

Status Withdrawn
Number of pages 32
Committee Transfusie, infusie en injectieapparatuur voor medische toepassingen
Published on 01-10-2003
Language English
This International Standard applies to safety and performance and testing requirements for single-use and multiple-use needle-free injection systems intended for human use in clinics and other medical settings and for personal use by patients. The dose chamber of the injection system 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 also may be a permanent internal chamber designed to last through the claimed life of the device. Excluded from this International Standard 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.


ICS-code 11.040.20
Dutch title Naaldloze injectoren voor medisch gebruik - Eisen en beproevingsmethoden
English title Needle-free injectors for medical use - Requirements and test methods
Replaced by

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