Laboratory testing - Import export

Sensitiv imago® 530 is the previous model in the SensitivE line. Hi-tech hardware-software complexes for diagnostic scan, analysis and healing of organism. Senstiv imago 530 device is being assembled according to the new European quality management standards 9001 full accepted in EU in 2013. The device passed the medical laboratory testing class 2, according to the European Directive.

Declaration of conformity is a document that certifies conformity of the products being released (released) to the requirements of statutory documents including the technical regulations of the Customs Union. Depending on the scheme applied the products conformity assessment in the form of declaring of conformity is to be performed on the basis of applicant’s own evidence and (or) evidence obtained involving the accredited test laboratory and (or) certification authority. Declaration of conformity has equal legal force with the certificate. At the applicant’s will, if provided for by the technical regulations, declaring can be substituted with certification. declaration of conformity shall be executed on a mandatory basis, the forms of voluntary products conformity declaring do not exist