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SES Conclusion for Medical Products Not Required Anymore for Customs Clearance

28/ 02/ 2018
  On February 2nd, 2018 Resolution of the Cabinet of Ministers No. 44 dated January 31st, 2018 On Amendments to Resolution of the Cabinet of Ministers of Ukraine No. 1031 dated October 5th , 2011 and No. 256 dated May 25th, 2016 came into force. With the entry into force of the resolution, the list of goods that were not subject to sanitary-epidemiological control (including in the form of preliminary documentary control) at crossing the customs control zone was expanded. Therefore, Ukrainian legislation does not require to provide the SES conclusion at customs clearance for medical products, medical products for in vitro diagnosis and aids to them, as well as active implantable medical products that have passed the procedure for assessing compliance with the requirements of technical regulations.
On February 2nd, 2018 Resolution of the Cabinet of Ministers No. 44 dated January 31st, 2018 “On Amendments to Resolution of the Cabinet of Ministers of Ukraine No. 1031 dated October 5th , 2011 and No. 256 dated May 25th, 2016″ came into force.

With the entry into force of the resolution, the list of goods that were not subject to sanitary-epidemiological control (including in the form of preliminary documentary control) at crossing the customs control zone was expanded.

Therefore, Ukrainian legislation does not require to provide the SES conclusion at customs clearance for medical products, medical products for in vitro diagnosis and aids to them, as well as active implantable medical products that have passed the procedure for assessing compliance with the requirements of technical regulations.

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