93/42 / EEC Medical Device Directive was published by the Ministry of Health , since January 1, 2004, that if products carry the CE mark, they will accept in the European Union and Turkey’ borders. All MEDİSPO’ branded products have CE mark in accordance with the legislation since 2008. Accordingly, the main topics of our company’s quality policy are as follows;
To work in compliance with all laws and rules in the medical device industry,
To fulfill all the requirements of the quality system at all stages of production,
To implement the training processes required to keep the product quality up to date,
To develop the product range by considering customer demands,
To ensure that all product groups comply with the prescribed specifications.