ASTM F 2394 : 2007 : R2017
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Standard Guide for Measuring Securement of Balloon Expandable Vascular Stent Mounted on Delivery System
Hardcopy , PDF
18-10-2022
English
08-09-2017
CONTAINED IN VOL. 13.01, 2017 Gives 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.
Committee |
F 04
|
DocumentType |
Guide
|
Pages |
13
|
ProductNote |
Reconfirmed 2017
|
PublisherName |
American Society for Testing and Materials
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
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 may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard.
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 and health practices and determine the applicability of regulatory requirements 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.
ASTM F 3206 : 2017 | Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies |
ASTM F 3036 : 2013 | Standard Guide for Testing Absorbable Stents |
ASTM F 3036 : 2021 | Standard Guide for Testing Absorbable Stents |
ASTM E 1169 : 2017 : EDT 1 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2014 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1488 : 2009 | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
ASTM E 1169 : 1989 : R1996 | Standard Guide for Conducting Ruggedness Tests |
ASTM E 1169 : 2018 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1488 : 2002 : EDT 1 | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
CFR 21(PTS800-1299) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 800-1299 |
ASTM E 1169 : 2021 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2017 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2002 | Standard Guide for Conducting Ruggedness Tests |
ASTM E 1488 : 2008 | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
ASTM E 1488 : 1996 | Standard Guide for Statistical Procedures to Use in Developing and Applying ASTM Test Methods |
ASTM E 1488 : 2008 : REV A | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
ISO 10555-1:2013 | Intravascular catheters — Sterile and single-use catheters — Part 1: General requirements |
ASTM E 1488 : 2012 : R2018 | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
ASTM E 1488 : 2012 : EDT 1 | Standard Guide for Statistical Procedures to Use in Developing and Applying Test Methods |
ASTM E 1169 : 2007 | Standard Practice for Conducting Ruggedness Tests |
EN 14299:2004 | Non active surgical implants - Particular requirements for cardiac and vascular implants - Specific requirements for arterial stents |
ASTM E 1169 : 2013 : REV A | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2012 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2020 | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2012 : REV A | Standard Practice for Conducting Ruggedness Tests |
ASTM E 1169 : 2013 | Standard Practice for Conducting Ruggedness Tests |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.