Kiwa Notified Body for Medical Devices
Within the Kiwa group, Kiwa Cermet Italia (NB 0476) and Kiwa Belgelenddirme Hizmetleri in Turkeij (NB 1984) are notified for the medical devices directive MDD 93/42 / EEC. 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.
Are you located in the EU or North- or South-America? Please contact Kiwa Italia.
Are you located in Asia and Africa? Please contact Kiwa Turkey.
More than twenty years of experience
Kiwa boasts a wide and in-depth experience as Notified Body from over 20 years in medical devices certification, with thousands of products already certified according to the MDD 93/42/EEC Directive and subsequent amendments.
Member of TEAM-NB
Kiwa Cermet Italia and Kiwa Turkey are members of TEAM-NB, the European Association Medical devices of Notified Bodies.