1 Scope
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:
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— 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);
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— generate aerosols, droplets, powders or other formulations for inhalation, insufflation,
intranasal or oral deposition (such as sprays, inhalers, misters);
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— 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);
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— apply sonic or electromagnetic energy (such as ultrasonic or iontophoretic devices);
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— infusion systems for adding or metering medication into or through systems of artificial
tubes, catheters, and/or needles which themselves enter the body.