ADOPTED_FROM:CEN/TR 16961:2018
The purpose of this document is to indicate how to present the uncertainty data determined by EN ISO 12999-1 in a laboratory test report of the Sound reduction index R of a building product or a building system, determined in accordance with EN ISO 717-1 and EN ISO 10140-2:2010, Figure B.1. It is planned to include this information in EN ISO 10140-2.
Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
