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Description of 20/30385404 DC 2020This 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.
About BSIBSI Group, also known as the British Standards Institution is the national standards body of the United Kingdom. BSI produces technical standards on a wide range of products and services and also supplies certification and standards-related services to businesses. |
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