ASTM F 2211 Standard Classification for Tissue Engineered Medical Products (TEMPs)
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ASTM F 2211 Document Information:
Title
Standard Classification for Tissue Engineered Medical Products (TEMPs)
ASTM International
Publication Date:
Oct 1, 2004
Scope:
This classification outlines the aspects of tissue engineered medical
products that will be
developed as standards. This classification excludes traditional
transplantation of organs and
tissues as well as transplantation of living cells alone as cellular
therapies.
This classification does 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.
This standard does not purport to address specific components coverd
in other standards. Any safety
areas associated with the medical product's use will not be addressed
in this standard. 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 requirements
prior to use.
Keywords:
- biomaterials
- biomolecules
- cells
- classification
- TEMPs
- tissue-engineering
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