ASTM F2038-00(2011)
Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part Imdash;Formulations and Uncured Materials
- Standard No.
- ASTM F2038-00(2011)
- Release Date
- 2000
- Published By
- American Society for Testing and Materials (ASTM)
- Status
- Replace By
- ASTM F2038-18
- Latest
- ASTM F2038-18
- Scope
4.1 This guide is intended to provide guidance for the specification and selection of silicone materials for medical device applications.
Silicone manufacturers supplying materials to the medical device industry should readily provide information regarding non-proprietary product formulation to their customers either directly, or through the US FDA master file program.
1.1 This guide is intended to educate potential users of silicone elastomers, gels, and foams relative to their formulation and use. It does not provide information relative to silicone powders, fluids, and other silicones. The information provided is offered to guide users in the selection of appropriate materials, after consideration of the chemical, physical, and toxicological properties of individual ingredients or by-products. This guide offers general information about silicone materials typically used for medical applications. Detail on the crosslinking and fabrication of silicone materials is found in Part II of this guide.
1.2 Fabrication and properties of elastomers is covered in the companion document, F604, Part II. This monograph addresses only components of uncured elastomers, gels, and foams.
1.3 Silicone biocompatibility issues can be addressed at several levels, but ultimately the device manufacturer must assess biological suitability relative to intended use.
1.4 Biological and physical properties tend to be more reproducible when materials are manufactured in accordance with accepted quality standards such as ANSI ISO 9001 and current FDA Quality System Regulations/Good Manufacturing Practice Regulations.
1.5 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard.
1.6 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. Users are also advised to refer to Material Safety Data Sheets provided with uncured silicone components.
ASTM F2038-00(2011) Referenced Document
- ANSI/AAMI ST29 Recommended Practice for Determining Residual Ethylene Oxide in Medical Devices
- ANSI/AAMI ST41
- ANSI/AAMI ST50
- ASTM D1566 Standard Terminology Relating to Rubber
- ASTM F813 Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
ASTM F2038-00(2011) history
- 2018 ASTM F2038-18 Standard Guide for Silicone Elastomers, Gels and Foams Used in Medical Applications Part I - Formulations and Uncured Materials
- 2000 ASTM F2038-00(2011) Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part Imdash;Formulations and Uncured Materials
- 2005 ASTM F2038-00(2005) Standard Guide for Silicone Elastomers, Gels and Foams Used in Medical Applications Part I - Formulations and Uncured Materials
- 2000 ASTM F2038-00e1 Standard Guide for Silicone Elastomers, Gels and Foams Used in Medical Applications Part I - Formulations and Uncured Materials
- 2000 ASTM F2038-00 Standard Guide for Silicone Elastomers, Gels and Foams Used in Medical Applications Part I - Formulations and Uncured Materials
