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Normas BSI – AENOR
20/30385404 DC

20/30385404 DC

BS ISO 11608-6. Needle-based injection systems for medical use. Requirements and test methods. Part 6. On-body delivery systems

Fecha:
2020-02-18 /Definitive
Comité:
CH/84
Equivalencias internacionales:

ISO/DIS 11608-6

Resumen:

This document specifies requirements and test methods for On-Body Delivery Systems (OBDS), which are body-worn or patient-worn NISs for single patient use, intended for subcutaneous, intramuscular or intradermal delivery of a discrete volume (bolus) of medicinal product, through needles or soft cannulas, incorporating pre-filled or user-filled, replaceable or non-replaceable containers.

NOTE 1

Although technically a device using a soft cannula is not “needle-based”, the soft cannula is placed by a needle and can be included in this classification.

NOTE 2

Some requirements and methods are already established and included in other parts of the ISO 11608 series. To ensure consistency, these requirements will not be repeated in this document, but referenced.

Infusion pumps which are not body or patient worn, or those that are designed for continuous delivery at a specific rate required to achieve and/or maintain a desired plasma medicinal product concentration, are excluded from this document and may be covered by IEC 60601-2-24 (if electronic) or ISO 28620 (if non-electronic). However, while this document is not intended to directly apply to these pump products, it does contain requirements and tests methods that can be used to help design and evaluate them.

Keywords:
Medical instruments, Fluid equipment, Injection instruments, Examination (medical), Medical sciences, Safety requirements
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