SOOFT italia, a OOgroup company, has obtained CE mark approval for its iontophoresis device for corneal cross-linking. The device, which includes Ricrolin+ and a new Power Generator I-ON CXL, allows the riboflavin to penetrate in the ...
Tags: SOOFT italia, CE mark, corneal cross linking
The 24th China International Glass Industrial Technical Exhibition (China Glass 2013) is around the corner. This event will take place in Beijing on 24-27 May 2013. More than 800 companies from 30 countries are expected to attend this glass ...
The British Standards Institution (BSI) has granted ISO 13485:2003 certification to Cardium Therapeutics' Excellagen advanced wound care gel product. Excellagen, which is designed for application at only one-week intervals, is a fibrillar ...
MakieLab also picks up an Entertainment and Gaming award. Over 100,000 digital Makie doll characters have been created to date. The news comes as creator of the 3D printed dolls, MakieLab, is honoured at the SXSW 5th Annual Accelerator ...
Tags: makielab, Digital Makie, Gaming
Abbott has presented clinical study data from a Endovascular Valve Edge-to-Edge REpair STudy (EVEREST II ) High Surgical Risk cohort of its MitraClip System for the treatment of mitral regurgitation (MR). The CE-marked catheter-based ...
Tags: clinical study, MitraClip System, medical
Medtronic has obtained CE mark certification from the European Union for its Attain Performa portfolio of quadripolar leads. The quadripolar leads are compatible with the company's Viva/Brava Quad cardiac resynchronization therapy ...
Tags: Medtronic, CE mark certification, Attain Performa portfolio
Boston ScientificBoston Scientific, a manufacturer of medical devices, is now offering Rubicon Support Catheter in 0.035" and 0.018" diameters in the US. The FDA-approved and CE-marked device, which provides various functionalities such ...
Tags: Boston Scientific, medical devices, Rubicon Support Catheter
CircuLite has obtained conditional approval from the US Food and Drug Administration (FDA) for its Synergy Circulatory Support System, designed for reversing the symptoms of heart failure in ambulatory chronic heart failure patients. The ...
Tags: CircuLite, FDA Conditional Approval, Micro-Blood Pump Device
Cohera Medical has treated the first patient in a US no-drain clinical study of its TissuGlu Surgical Adhesive, designed for use during large flap surgeries such as abdominoplasty (tummy tuck). The CE-marked internal surgical adhesive ...
Tags: Cohera Medical, no-drain clinical study, TissuGlu Surgical Adhesive
CeQur has reported its PaQ insulin delivery device initial study data at the 6th International Conference on Advanced Technologies & Treatments for Diabetes (ATTD) in Paris, France. The discreet, wearable CE-marked device, which comprises ...
Tags: CeQur, PaQ insulin delivery device, insulin infuser reservoir
Canton Fair has reached new attendance peak in 2012 No doubt, the Canton Fair with its ever expanding exhibition buildings and numbers of visitors is an impressive event. Yet the ever growing exhibition space and amount of suppliers makes a ...
Tags: Focus Vision, China, Canton Fair Visit, economy
The British Standards Institute (BSI) has awarded ISO 13485: 2003 certification to Zyomyx's quality management system. Zyomyx is involved in developing and commercializing proprietary diagnostic platforms including quantitative disposable ...
Tags: Zyomyx, CD4 diagnostics, proprietary diagnostic platforms
Medtronic has gained CE mark approval for its Engager transcatheter aortic valve implantation (TAVI) system with transapical delivery catheter, from the European Union (EU). The new TAVI system, which is inserted in the apex (the lower, ...
Tags: Medtronic, transcatheter aortic valve implantation, TAVI
Congatec has ported the Windows Embedded Compact 7 operating system to a Qseven embedded module based on the Freescale i.MX6 ARM Cortex-A9 processor. Windows Embedded Compact 7 (WEC7) is the latest generation of Windows CE operating ...
Tags: Congatec, Windows Embedded Compact 7 operating system, company news
PneumRx has treated the first US patient in a FDA-approved RENEW clinical study of its RePneu lung volume reduction coil (LVRC), designed to treat severe emphysema. Made from shape-memory Nitinol, the CE-marked minimally invasive medical ...
Tags: PneumRx, lung volume reduction coil, FDA