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ASTM F3575-24

Standard Guide for Model Development for Particulate Generation Testing of Endovascular Devices

Standard Guide for Model Development for Particulate Generation Testing of Endovascular Devices F3575-24 ASTM|F3575-24|en-US Standard Guide for Model Development for Particulate Generation Testing of Endovascular Devices Standard new BOS Vol. 13.02 Committee F04
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Significance and Use

5.1 The evaluation of particulates from endovascular devices is a critical parameter to help ensure that the devices can be delivered to and from the treatment site with minimal unintended effects due to particulate generation.

5.2 This guide is intended for the development and design of a simulated use model for the evaluation of particulate generation by those manufacturing and/or evaluating endovascular devices.

5.3 This guide may be useful for establishment of credibility of a simulated use model as part of development testing and regulatory submission testing and filings.

Scope

1.1 This standard provides recommendations regarding the development of a simulated use model for particulate generation testing of endovascular devices.

1.2 Corresponding recommendations will be provided for the coronary, peripheral, and neurovascular anatomy respectively, as these different environments each have unique challenges and considerations that should be incorporated into the model development.

1.3 Considerations include, but are not limited to: anatomical considerations (for example, tortuosity, dimensions, disease state), working path length of the human vasculature, model/device interactions (for example, material properties, vessel straightening due to device placement), and device/device interactions (for example, use of delivery catheters and/or guide wires).

1.4 Standardizing the model development allows for better interpretation of the test results and comparison of performance of similar medical devices.

1.5 Explicit models for devices (or groups of devices) are not provided in this document as specific device attributes (for example, device flexibility, device material), anatomical target locations, and intended patient population can strongly impact model design. This document enables the development of a model that appropriately and sufficiently challenges the subject device with respect to particulate generation.

1.6 While this document is intended to aid in the development and design of the simulated use model for the assessment of particulate generation, additional information regarding the evaluation of the particulate matter and particulate measurements can be found in AAMI TIR 42. Similarly, this document is not intended to address testing associated with the use of the model.

1.7 This 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.

1.8 This 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.

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Details
Book of Standards Volume: 13.02
Developed by Subcommittee: F04.30
Pages: 5
DOI: 10.1520/F3575-24
ICS Code: 11.040.40