
ISO 10993:2015
ISO 10993:2015 Biological evaluation of medical devices – Part 33: Guidance on tests to evaluate genotoxicity – Supplement to ISO 10993-3
CDN $336.00
SKU: 59099956da18
Category: ICS:11.100.20
Description
There are differences between the views of regulatory bodies on the subject of genotoxicity testing. The purpose of this ISO/TR 10993-33: 2015 is to provide background information to facilitate the selection of tests and guidance on the performance of tests.
Edition
1
Published Date
2015-03-06
Status
PUBLISHED
Pages
47
Format 
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment
Abstract
There are differences between the views of regulatory bodies on the subject of genotoxicity testing. The purpose of this ISO/TR 10993-33: 2015 is to provide background information to facilitate the selection of tests and guidance on the performance of tests.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-

ISO 10993:2017 Biological evaluation of medical devices – Part 11: Tests for systemic toxicity
CDN $333.00 Add to cart -

ISO 17593:2022 Clinical laboratory testing and in vitro medical devices – Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
CDN $379.00 Add to cart -

ISO 11796:2023 Biological evaluation of medical devices – Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices
CDN $295.00 Add to cart -

ISO 22442:2020 Medical devices utilizing animal tissues and their derivatives – Part 2: Controls on sourcing, collection and handling
CDN $186.00 Add to cart







