Documentation
Medical Device Regulation (MDR)
Careturner A/S confirms that our products – Careturner as well as Soft Tilt for Invacare has been tested and approved by TÜV and fulfills the relevant standards. We certify that the product complies with the essential requirements defined in the Medical Device Directive standards and satisfies the Medical Device Regulation 2017/745 (MDR). Our product is classified in Class 1.
Our product has gone through intensive tests at hospitals and nursing homes and we have described many positive business cases together with our customers – reports we can supply by request.
Please also read our Declaration of Conformity
