Biological evaluation of medical devices - Tests for genotoxicity, carcinogenicity and reproductive toxicityBS EN ISO 10993 3 specifies strategies for hazard identification and tests on medical devices for the biological aspects of genotoxicity, carcinogenicity, and reproductive and developmental toxicity. It is applicable for evaluation of a medical device whose potential for genotoxicity, carcinogenicity or reproductive toxicity has been identified. Guidance on selection of tests is provided in BS EN ISO 10993 1.

The information exchange model reflects the whole active functionality of the server

This document applies to parabolic-trough collectors equipped with the manufacturer-supplied sun tracking mechanism

service or process involved

Creation and destruction of BIP links

Requirements governing domain of applicability

helps ensure adequate safety and protection against hazards presented by the use of gas

6:1990 is applicable to the species and grades of timber given in BS 5268-2

Determination of nitrogen content

BS EN 15696 gives recommendations on:

are assumed to be small compared with the wavelengths of the interfering signals

Such benefits are most often associated with the application of a number of key principles and attributes in the design and implementation of the asset management system

The emission limits given are on the basis that the equipment of the product family range is installed in railway substation areas