As İnceler Medikal Health Services Industry Trade Limited Company, we embrace a multidisciplinary working system and market our products, which are approved and certified by the Dutch accreditation company KIWA according to the requirements of EN ISO 13485:2016 and Annex II of the Medical Device Directive 93/42/EEC. We are currently working on the transition to the EU 2017/745 MDR Annex IX quality management system to bring our company and products up to international standards. We also play an active role in the US market as a manufacturer registered with the FDA.
Our company has implemented its production and management plans in accordance with international standards, and our quality department has made it a principle to provide prompt support to customers regarding their requests and needs. Furthermore, as part of our quality policy, customer satisfaction, both before and after sales, is paramount. Therefore, to maintain our relationships and keep our brand open to development, we strive to provide the best possible service through surveys and customer feedback, which we constantly monitor.
