ISO/TS 37137-1:2021 PDF
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Biological evaluation of absorbable medical devices — Part 1: General requirements
This document specifies the requirements for the evaluation of absorbable medical devices during a biological risk assessment based on ISO 10993-1, including a clarification of the terms “absorb”, “degrade” and other related terms (see Annex A).
| Edition | 2021 |
|---|---|
| Standard Part No | 1 |
| Published Date | 2021 |
| Published By | ISO/TS |
| Page Count | 12 |
