ASTM F1027-86(1995)e1 - 1.1.1995
 
1. Scope

1.1 This practice describes a procedure to assess the cytotoxic potential of materials for use in the construction of medical materials and devices using human excised donor (HED) tissues and their derived primary cells taken from the orofacial region.

1.2 This practice may be used either directly to evaluate materials or as a reference against which other cytotoxicity methods may be compared.

1.3 This practice is one of a series of reference methods for assessment of cytotoxic potential, employing different techniques.

1.4 Assessment of cytotoxicity is one of several procedures employed in determining the biological response to a material, as recommended in Practice F748.

1.5 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.

 
2. Referenced Documents

D883-24

Standard Terminology Relating to Plastics

F748-16

Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices

F813-20

Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices

F703-18(2022)

Standard Specification for Implantable Breast Prostheses

F604-94

Specification for Silicone Elastomers Used in Medical Applications (Withdrawn 2001)