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ASTM F 2394 : 2007 : R2022

Current

Current

The latest, up-to-date edition.

Standard Guide for Measuring Securement of Balloon-Expandable Vascular Stent Mounted on Delivery System

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

12-10-2022

1.1This guide provides guidance for the design and development of pre-test treatments, tests, and test endpoints to measure stent securement of pre-mounted, unsheathed, balloon-expandable stent delivery systems. This guide is intended to aid investigators in the design, development, and in vitro characterization of pre-mounted, unsheathed, balloon-expandable stent delivery systems.

1.2This guide covers the laboratory determination of the shear force required to displace or dislodge a balloon-expandable endovascular stent mounted on a delivery system. The guide proposes a set of options to consider when testing stent securement. The options cover pre-test treatments, possible stent securement tests, and relevant test endpoints. An example test apparatus is given in 7.1.

1.3This guide covers in vitro bench testing characterization only. Measured levels of securement and product design/process differentiation may be particularly influenced by selections of pre-test treatments, securement test type (for example, stent gripping method), and test endpoint. In vivo characteristics may also differ from in vitro results.

1.4This guide does not cover all possible pre-test treatments, stent securement tests, or test endpoints. It is intended to provide a starting point from which to select and investigate securement test options.

1.5This guide does not specify a method for mounting the stent onto the delivery system.

1.6The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.

1.7This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

1.8This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Committee
F 04
DocumentType
Guide
Pages
13
PublisherName
American Society for Testing and Materials
Status
Current
Supersedes

ASTM F 3206 : 2017 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
ASTM F 3036 : 2021 Standard Guide for Testing Absorbable Stents

ASTM E 1488 : 2012 : R2023 Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods
ASTM E 1488 : 2023 Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods
ASTM E 1488 : 2012 : R2018 Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods

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£57.60
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