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What is IEC 6060122Ed72018

The IEC 60601-2-2 standard, edition 7:2018, is a technical document that provides requirements for the basic safety and essential performance of high-frequency surgical equipment. This standard was developed by the International Electrotechnical Commission (IEC) in collaboration with medical device manufacturers, healthcare professionals, and regulatory authorities.

Scope and Purpose

The scope of IEC 60601-2-2 is to ensure the safety of both patients and operators when using high-frequency surgical equipment. This standard applies to equipment used in various medical procedures, such as cutting, coagulation, and tissue removal, where high-frequency electrical energy is applied to or removed from the patient.

The purpose of this standard is to establish general requirements for the design, manufacturing, labeling, and testing of high-frequency surgical equipment. It aims to minimize risks associated with electrical hazards, mechanical hazards, and other potential dangers that could arise from the use of this equipment.

Main Requirements

IEC 60601-2-2 specifies several requirements that high-frequency surgical equipment must meet. These include:

Electrical Safety: The equipment should be designed and manufactured to prevent electrical shocks, fires, and other electrical hazards. It should also comply with relevant national and international electrical safety standards.

Mechanical Safety: The equipment should be mechanically stable, secure, and easy to use. Users should not face any risk of injury due to equipment malfunction, tip-over, or instability.

Compatibility: The equipment should be compatible with other medical devices and systems commonly used in surgical settings. It should not interfere with the functionality or safety of other devices.

Information and Marking: The equipment should have clear and visible labels, warnings, and instructions for use. It should provide relevant information about its intended use, potential risks, and recommended maintenance procedures.

Conformity Assessment and Compliance

Manufacturers of high-frequency surgical equipment are responsible for ensuring their products comply with IEC 60601-2-2. They must perform various tests and assessments to demonstrate conformity before placing their equipment on the market.

Regulatory authorities and certification bodies may also conduct inspections and audits to verify compliance with this standard. Non-compliance can result in penalties, recalls, or even legal consequences for manufacturers.

In conclusion, IEC 60601-2-2 is a crucial standard for the safety and performance of high-frequency surgical equipment. By adhering to the requirements outlined in this document, manufacturers can ensure that their products are safe, reliable, and fit for medical use. Healthcare professionals and patients can trust that these devices meet stringent safety standards, minimizing the risk of accidents and ensuring effective medical interventions.


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