AS IEC 60601.1.9:2017 PDF
The objective of this Standard is to improve the environmental impact for the entire range of medical equipment (ME), taking into account all stages of the product life cycle: product specification, design, manufacturing, sales, logistics, installation, use and end of life management.
International standard IEC 60601-1-9 has been prepared by IEC subcommittee 62A: Common aspects of electrical equipment used in medical practice, of IEC technical committee 62: Electrical equipment in medical practice.
The first edition of this publication constitutes a collateral standard to IEC 60601-1: Medical electrical equipment – Part 1: General requirements for safety and essential performance hereafter referred to as the general standard.
This publication has been drafted in accordance with the ISO/IEC Directives, Part 2.
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