30.118

Due to market price fluctuations, if you need to purchase or consult the price. You can contact us or emial to us:   sales@allicdata.com

30.118 is a standard issued by the International Electrotechnical Commission (IEC), which refers to the equipment safety requirements and the protection criteria of emergency related personnel for health care applications. It specifies requirements concerning the protection requirements for the general safety of euipment used in the medical field as well as for the health care personnel working with it, such as design, construction, testing, user access and maintenance of the equipment.

The 30.118 application field covers a wide range of medical equipment, including medical imaging equipment, medical therapy equipment, diagnostics equipment, medical laboratory and testing equipment, patient monitor and support systems. In addition, it also covers all electrical medical systems, such as hospital information systems, laboratory information systems and the like that are used for the management of medical data.

The 30.118 provides technical safety requirements covering all aspects of engineering and safety, including but not limited to safety during normal operation, safety during maintenance and commissioning, safety during transport, accidental protection and protection against hazardous parts. Moreover, the standard also includes requirements for security of data exchanged between the medical system and external systems, as well as procedures for maintaining a secure system.

In order to ensure compliance with the 30.118 standard, equipment manufacturers must carry out a number of tests and assessments, such as risk analysis, fail-safe analysis, electromagnetic compatibility (EMC) tests, and environmental tests. Furthermore, manufacturers must also carry out an audit of their system in order to ensure it meets the requirements outlined in the standard.

The working principle of 30.118 is based on the principle of prevention. It is aimed at helping to prevent the occurrence of hazards and risks associated with medical equipment. Through the evaluation of the system\'s safety characteristics, the potential risks to personnel and the environment can be minimized. The standard also specifies the required minimum safety requirements for the equipment and the systems used in medical fields.

The 30.118 standard is a comprehensive document that provides detailed instructions and information relating to the safe and secure use of medical equipment. The application of this standard is essential to ensure the safety of any medical equipment used in the medical field, as well as the safety of personnel working with it. It is important to note that the requirements and guidance outlined in the standard are not exhaustive, and manufacturers must also assess the risk associated to their specific products to ensure that they meet the requirements of the standard.

The specific data is subject to PDF, and the above content is for reference