ISO/TS 37137-1:2021
Current
The latest, up-to-date edition.
Biological evaluation of absorbable medical devices — Part 1: General requirements
Hardcopy , PDF
English
12-03-2021
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).
| DocumentType |
Technical Specification
|
| Pages |
12
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Standards | Relationship |
| ABNT ISO/TS 37137-1:2026 | Identical |
| PD ISO/TS 37137-1:2021 | Identical |
| I.S. EN ISO 10993-1:2025 | Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO 10993-1:2025) |
| I.S. EN ISO 10993-12:2021 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021) |
Please Login or Create an Account so you can add users to your Multi user PDF Later.
Important note : All end users must be registered with an Account prior to user licenses being assigned.
Users cannot be edited or removed once added to your Multi user PDF.