KGZ/66
WTO/TBT
KG Kirgisische Republik
  • 30 - Pharmazeutische Erzeugnisse
  • 90 - Optische, fotografische oder kinematografische Instrumente, Apparate und Geräte; Mess-, Prüf- oder Präzisionsinstrumente, -apparate und -geräte; medizinische und chirurgische Instrumente, Apparate und Geräte; Teile und Zubehör für diese
  • 94 - Möbel; medizinisch-chirurgisches Mobiliar; Bettzeug und dergleichen; Beleuchtungskörper, anderweit weder genannt noch inbegriffen; Reklameleuchten, Leuchtschilder und ähnliche Waren; vorgefertigte Gebäude
2026-06-14
2026-05-20

Cotton wool, gauze, bandages and similar articles (for example, bandages, Band-Aids, poultices), impregnated or coated with pharmaceutical substances or packaged in forms or packages for retail sale, intended for use in medicine, surgery, dentistry or veterinary medicine (HS 3005); Devices and instruments used in medicine, surgery, dentistry or veterinary medicine, including scintigraphic equipment, other electro-medical equipment and vision testers (HS 9018); Equipment based on the use of X-ray, alpha, beta or gamma radiation, intended or not intended for medical, surgical, dental or veterinary use, including X-ray or radiotherapy equipment, X-ray tubes and other X - ray generators, high-voltage generators, shields and control panels, screens, tables, chairs and similar products for examination or treatment (HS 9022); Medical, surgical, dental or veterinary furniture (for example, operating tables, examination tables, hospital beds with mechanical devices, dental chairs); barber chairs and similar chairs with devices for rotating and simultaneously for tilting and lifting; parts of the above-mentioned products (HS Code 9402).

Draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices; (2 page(s), in Russian)

The draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices provides for the possibility of suspending the validity of the marketing authorization in the event that there is no valid report on the results of inspection in the marketing authorization application of a medical device in order to prevent the release into circulation of a poor quality medical product.