Kiwa is a global leader in Testing, Inspection and Certification (TIC) market. With our services, we create trust in our customers products, services, processes, management systems and personal capabilities and we help them to improve.
Within the Kiwa Group, Kiwa Italy and Kiwa Turkey are Notified Bodies and can assess if medical devices with medium or high risk meet the legal requirements according to the MDD 93/42/EEC Directive. If the devices meet the requirements, they can be admitted to the European market and be CE marked.
Kiwa has the ability to supply the tools for the conformity evaluation, according to what is set by the MDD and subsequent amendments or by optional technical regulations.