İnceler Medikal Sağlık Hizmetleri Sanayi Ticaret Limited Şirketi adopts a multidisciplinary working system, and we market our products that have been approved and certified by the Dutch-based KIWA accreditation company in accordance with EN ISO 13485:2016 and Medical Device Regulation 93/42/EEC Annex-II requirements. To bring our company and our products to international standards, we continue to work on the transition to the EU 2017/745 MDR ANNEX-IX quality management system. At the same time, we play an active role in the US market as a registered manufacturer in the FDA database.

Our company has carried out its production and management plans in accordance with international standards and has adopted the principle of providing instant support to customers in their requests and needs by the quality department. In addition, due to our quality policy, the pre-sales and after-sales satisfaction of our customers is very important to us. For this reason, we are working to provide the best technical service with our surveys and customer relations, which we always ensure to be traceable, to maintain our relations and keep our brand open to development.