Implants for surgery. Cardiac pacemakers - Reporting of clinical performance of populations of pulse generators or leads Ingestion-build-89079 Directive 2006/95/EC of the European

Directive 2006/95/EC of the European Parliament

or installed equipment to measure photon radiation about

and other products intended to bear the mass of one or more children

access to work station

Implants for surgery. Cardiac pacemakers - Reporting of clinical performance of populations of pulse generators or leads Ingestion-build-89079 Directive 2006/95/EC of the European1 Scope This part of ISO 5841 specifies requirements for reports on the clinical performance in humans of population samples of cardiac pulse generators or leads, intended for long term implantation, hereinafter referred to as devices. Devices to be reported has to be market approved in one or more geographies. It includes general requirements for all reports and supplementary requirements for reports on cumulative experience with devices and