European Medical Device Technology, November/December 2013, Volume 4, No. 5


November 26th, 2013


This Issue's Articles
Medical and in vitro diagnostic device manufacturers soon will need to comply with European requirements restricting the use of certain hazardous substances in electrical and electronic equipment. By: Maria E. Donawa

To successfully extrude medical tubing, a number of factors must be considered, including the manufacturing environment, material properties and the function of the finished device.

Overshadowed by the BRIC countries, Turkey, Indonesia and Iran don’t get the attention they deserve. Here’s why they should be on the global medtech industry’s radar.