ASTM F 2312 : 2011
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Standard Terminology Relating to Tissue Engineered Medical Products
Hardcopy , PDF
04-06-2020
English
01-04-2011
Important note : Users cannot be edited or removed once added to your Multi user PDF.| Committee |
F 04
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| DocumentType |
Reference Material
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| Pages |
9
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| PublisherName |
American Society for Testing and Materials
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| Status |
Superseded
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| SupersededBy | |
| Supersedes |
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.
| ASTM F 3209 : 2016 | Standard Guide for Autologous Platelet-Rich Plasma for Use in Tissue Engineering and Cell Therapy |
| ASTM F 2903 : 2011 | Standard Guide for Tissue Engineered Medical Products (TEMPs) for Reinforcement of Tendon and Ligament Surgical Repair (Withdrawn 2020) |
| ASTM F 3163 : 2016 | Standard Guide for Classification of Cellular and/or Tissue-Based Products (CTPs) for Skin Wounds |
| ASTM F 2383 : 2011 | Standard Guide for Assessment of Adventitious Agents in Tissue Engineered Medical Products (TEMPs) (Withdrawn 2020) |
| ASTM F 3368 : 2019 | Standard Guide for Cell Potency Assays for Cell Therapy and Tissue Engineered Products |
| ASTM F 2791 : 2015 | Standard Guide for Assessment of Surface Texture of Non-Porous Biomaterials in Two Dimensions |
| ASTM F 2997 : 2013 | Standard Practice for Quantification of Calcium Deposits in Osteogenic Culture of Progenitor Cells Using Fluorescent Image Analysis |
| ASTM F 3225 : 2017 | Standard Guide for Characterization and Assessment of Vascular Graft Tissue Engineered Medical Products (TEMPs) |
| ASTM F 3106 : 2014 | Standard Guide for <emph type="bdit">in vitro</emph> Osteoblast Differentiation Assays |
| ASTM F 2150 : 2013 | Standard Guide for Characterization and Testing of Biomaterial Scaffolds Used in Tissue-Engineered Medical Products |
| ASTM F 3369 : 2019 : EDT 1 | Standard Guide for Assessing the Skeletal Myoblast Phenotype |
| ASTM F 2664 : 2019 : EDT 1 | Standard Guide for Assessing the Attachment of Cells to Biomaterial Surfaces by Physical Methods |
| ASTM F 3223 : 2017 | Standard Guide for Characterization and Assessment of Tissue Engineered Medical Products (TEMPs) for Knee Meniscus Surgical Repair and/or Reconstruction |
| ASTM F 3224 : 2017 | Standard Test Method for Evaluating Growth of Engineered Cartilage Tissue using Magnetic Resonance Imaging |
| ASTM F 2664 : 2011 | Standard Guide for Assessing the Attachment of Cells to Biomaterial Surfaces by Physical Methods |
| ASTM F 3142 : 2016 | Standard Guide for Evaluation of <emph type="bdit">in vitro</emph> Release of Biomolecules from Biomaterials Scaffolds for TEMPs |
| ASTM F 2315 : 2018 | Standard Guide for Immobilization or Encapsulation of Living Cells or Tissue in Alginate Gels |
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