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ASTM F2312-03

Historical Revision

Standard Terminology Relating to Tissue Engineered Medical Products

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1.1 This 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.

1.2 The 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.

1.3 The 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.

1.4 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 and health practices and determine the applicability of regulatory limitations prior to use.


SDO ASTM: ASTM International
Document Number F2312
Publication Date Sept. 10, 2003
Language en - English
Page Count 6
Revision Level 03
Supercedes
Committee F04.41
Publish Date Document Id Type View
Oct. 1, 2024 F2312-24 Revision
April 1, 2011 F2312-11 Revision
June 1, 2010 F2312-10 Revision
Nov. 1, 2004 F2312-04 Revision
Sept. 10, 2003 F2312-03 Revision
Feb. 1, 2020 F2312-11R20 Reaffirmation