As a result of the new approach process initiated by the European Union in 1985, today more than twenty directives define the health and safety requirements of products.
While these directives define only the basic requirements and marking conditions, harmonized standards specially prepared for the product under the directives;
It includes details on scope, descriptions, structural requirements, documentation and tests.
These standards are prepared and published by institutions such as CEN, CENELEC and ETSI as a result of commission studies.
In order for the products to be placed on the market, manufacturers have to fulfill the requirements of the directive they are subject to and make CE marking in their products.
The European Union has defined the paths to be followed for CE marking under a total of 8 modules. When we examine the requirements of the modules to which the products are subjected, we come across a technical file definition.
Whether or not the notified body requirement is required, the technical files must be prepared completely by the manufacturer.
This marking made according to the relevant directive or directives is a legal obligation according to the law numbered 4703 in order to put the products on the market.
The technical files of the electrical products should include risk analysis, product description, user manuals, electrical diagrams, and sub-component definitions.
In addition to this, the technical file should contain the complete type of test reports, which were made strictly according to the relevant standard.
Lvt test laboratories offer a wide range of testing services to manufacturers, especially applications of lvd - emc - mdr and harmonized standards of machinery directives.
As our related scope can be examined from the Türkak website, our application areas are mostly switchgears, electrical panels, high voltage product groups, medical devices, information technology devices, machinery, electrical equipment used in the home environment and electric charging stations.