Legal notices

1.     Ritmedic authorized distributors and resellers are not selling on internet marketplaces. Unauthorized reselling of genuine Ritmscenar devices, selling Scenar device imitations as well as unauthorized usage of the registered trademarks Ritmscenar and/or Scenar for promotion through any channel including internet marketplaces or for any other purposes is an illegal act that will be prosecuted to the full extent of the law.

2.     In most countries, the use of (para)medical electrical devices class IIA on patients is not allowed without proof of having attended the minimum training as indicated by the manufacturer through a manufacturer approved training institute. All Ritmedic approved Scenar training is delivered by or under the supervision of medical doctors that have been assigned for this purpose. Without proof of training, the usage of such (para)medical devices on patients is considered as an illegal (para)medical practice and may lead to a fine and the general suspension of the therapeutic license of the practitioner by the Ministry of Health. Please check with your local RITM Group partner how to obtain the required manufacturer approved training for legal use of the Ritmscenar technology and methodology in your country.

3.     Ritmedic authorized distributors, resellers and trained practitioners only sell and use genuine Ritmscenars. Scenar devices have been worldwide classified as medical devices class IIA. In Europe, Scenar devices can only be obtained legally through Ritmedic. Ritmedic Ritmscenars are the only Scenar devices on the EU market that are compliant with the CE regulations and the EU Medical Device Directive (MDD) Council Directive 93/42/EEC for medical devices class IIA. This MDD has been integrally implemented in the laws of all the EU and EFTA countries. The import, promotion, sales and use of Scenar devices through other market channels is an illegal act according to the legislation and may lead to a fine and the suspension of the therapeutic license of the practitioner and the commercial license of the trader. In other parts of the world similar legislation is applicable. Please check with your local RITM Group partner which legislation is applicable in your country for the use of medical devices class IIA and how to obtain Ritmscenar devices and the required manufacturer approved training for legal use of the Ritmscenar technology and methodology in your country.

4.     In most countries, the use of (para)medical electrical devices class IIA which are not obtained through and supported by the official dealer network is considered as an illegal (para)medical practice and may lead to a fine and the general suspension of the therapeutic license of the practitioner by the Ministry of Health.

5.     In case of any questions regarding legal aspects of the use of Scenar devices please contact your local RITM Group representative or contact our legal department directly via legal@ritmgroup.com

SCENAR and RITMSCENAR are worldwide registered trademarks. Any use of these trademarks, other than agreed by legal contract with Kosmed International is an illegal act that will be prosecuted to the full extent of the law.