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In order to protect patient and user health, the European Union (EU) has made a major change in medical device directive with stricter requirements in order to improve quality, safety and performance data in medical devices and to harmonize all sector stakeholders, whether manufacturers, notified bodies or competent authorities.

Electrical equipment, which are parts of our daily lives, are brought into use in different models and types. As the importance of these products in our lives increases, safety problems for the health of the environment and human beings increases, too. In this context, the Low Voltage Directive has significance in the design and development of electrical products produced. 

LVD (Low Voltage Directive) is the directive relating to the electrical equipment designed for use within specific voltage limits. The aim of this directive is to determine the rules and procedures relating to the safety rules and compliance assessment procedures that are required for introduction of the electrical equipment included within the scope of the 

The aim of this directive is to determine the basic health and safety requirements to be met by lifts and lift security parts, requirements for introduction to the market relating to these products and principles of market surveillance and control.