Standard Terminology Relating to Tissue Engineered Medical Products

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-04-2020

Publisher

American Society for Testing and Materials

1.1This terminology defines basic terms and presents the relationships of the scientific fields related to Tissue Engineered Medical Products (TEMPs). Committee F04 has defined these terms for the specific purpose of unifying the language used in standards for TEMPs.

1.2The terms and relationships defined here are limited to TEMPs. They do not apply to any medical products of human origin regulated by the U.S. Food and Drug Administration under 21 CFR Parts 16 and 1270 and 21 CFR Parts 207, 807, and 1271.

1.3The terms and nomenclature presented in this standard are for the specific purposes of unifying the language used in TEMP standards and are not intended for labeling of regulated medical products.

1.4This 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.

1.5This 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	Reference Material
Pages	9
ProductNote	THIS STANDARD IS ALSO REFERS TO 21 CFR Parts 16 and 1270, 21 CFR Parts 207, 807, and 1271
PublisherName	American Society for Testing and Materials
Status	Current
Supersedes	ASTM F 2312 : 2011

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ASTM F 2315 : 2018	Standard Guide for Immobilization or Encapsulation of Living Cells or Tissue in Alginate Gels
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