RUS/99
WTO/TBT
RU Russie
  • 30 - Produits pharmaceutiques
  • 90 - Instruments et appareils d'optique, de photographie ou de cinématographie, de mesure, de contrôle ou de précision; instruments et appareils médico-chirurgicaux; parties et accessoires de ces instruments ou appareils
  • 94 - Meubles; mobilier médico-chirurgical; articles de literie et similaires; appareils d'éclairage non dénommés ni compris ailleurs; lampes-réclames, enseignes lumineuses, plaques indicatrices lumineuses et articles similaires; constructions préfabriquées
2020-04-20
2020-02-24

Wadding, gauze, bandages (dressings, adhesive plasters, poultices), impregnated or coated with pharmaceutical substances or in forms or packings for retail sale, for medical, surgical or veterinary use (HS 3005); Instruments and appliances used in medical, surgical, dental or veterinary sciences, including scintigraphic apparatus, other electro-medical apparatus and sight testing instruments (HS 9018); X-ray, alpha, beta, gamma radiation apparatus; x‑ray tubes, x-ray generators, high tension generators, control panels and desks, screens, examination or treatment tables, chairs and the like (HS 9022); Furniture; medical, surgical, dental or veterinary (e.g. operating tables, hospital beds, dentists' chairs) barbers' chairs; parts (HS 9402).

Draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices (104 page(s), in Russian)

The Draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices apply to medical devices issued for circulation in the territory of the Eurasian economic union and provide for the following: 

- clarification of terms and definitions; 

 - clarification of the mechanism for implementing the procedure for approval by States of the recognition of the expert opinion of the reference state; 

 - determination of cases when changes are made to the registration dossier of medical devices in the notification procedure; 

- clarification of the procedure for canceling the validity (cancellation) of the registration certificate of a medical device.

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