meddevice

medlatest critiques the world of the anodyne medical device corporate press release.

Mobihealth News has reported on what may be the first medical app to gain CE Mark approval in the UK.

California-based Biomerix Corporation has announced that it has received CE Mark approval for its ASSURE soft tissue repair mesh.

Commercial production of a new device that measures melanoma using photoacoustics, or laser-induced ultrasound, will soon be available to scientists and academia for cancer studies.

GI Dynamics, Inc. is to transition its EndoBarrier® Gastrointestinal Liner from clinical research status to commercial availability in Netherlands.

Cook Medical, is to invest up to €16.5m over four years creating highly skilled positions in Research and Development activities at its Limerick site, with Government support through IDA Ireland.

The 2012 International Medical Device Industry Compliance conference will take place in May at the Sheraton Stockholm Hotel, and will feature an illustrious list of guest speakers, no free pens and “buy your own” drinks.

Dutch Haemostasis and Regenerative Medicine company ProFibrix B.V., has announced that its U.S. multicenter Phase II clinical trial with Fibrocaps in spinal, peripheral vascular and general surgery resulted in a highly statistically significant reduction in mean time to haemostasis and incidence of haemostasis at 3, 5 and 10 minutes, as compared to active control.