Our valued Partner!
On 26 May 2021, EU Regulation 2017/745, also known as MDR, the European Union Act on Medical Devices, entered into force. On this basis, the Regulation requires new and more structured conditions for manufacturers of Medical Devices wishing to market their products within the European Union.
Our company is committed to comply with all legal provisions, therefore we have prepared our new EU Declarations of Conformity for all our products, and we have notified the required authority about our Class I products.
From below link you can download our ISO-13485 Certification and our EU Declaration of Conformity documents:
Metal walking aids and bathroom equipment:
Hospital and homecare furniture:
rev1 - 2021.05.26.