BIOTRONIK, pioneer of remote patient management solutions, has announced the introduction of a new online Quick View report designed to deliver improved efficiency when managing patients using BIOTRONIK Home Monitoring® technology.
Launches / Withdrawals
Boston Scientific Launches Coyote™ Balloon Catheter
Ultra-low profile, highly deliverable balloon dilatation catheter offers physicians exceptional performance in peripheral angioplasty procedures
MAQUET CARDIOVASCULAR RECEIVES FDA 510(K ) CLEARANCE AND CE MARK FOR ITS NEW SENSATION PLUS™ INTRA-AORTIC BALLOON CATHETER
MAQUET Cardiovascular, a leading provider of cardiovascular technologies, announced today that it has received both 510(k) clearance from the U.S. Food & Drug Administration (FDA) and CE mark approval for its new SENSATION PLUS™ 50cc 8 Fr. intra-aortic balloon catheter.
BD Launches a New Generation Short Peripheral IV Catheter to Reduce Risk of Blood Exposure to Healthcare Workers
A new generation of safety short peripheral IV catheter (SPIVC) technology designed to keep healthcare workers safe from needlestick injuries and blood exposure is now available from BD Medical.
NAVISCAN RECEIVES CE MARK APPROVAL FOR HIGH-RESOLUTION BREAST PET AND PET-GUIDED BIOPSY
NAVISCAN RECEIVES CE MARK APPROVAL FOR HIGH-RESOLUTION BREAST PET AND
PET-GUIDED BIOPSY: Positron Emission Mammography (PEM) Expands into 13 European Countries
Smith & Nephew introduces VERSAJET II, next-generation surgical wound care device
The Advanced Wound Management division of Smith & Nephew, has announced the launch of its VERSAJET II Hydrosurgery system for precise excision during surgical debridement.
St. Jude Medical Announces European Launch of Smaller Quadripolar Pacing System
St. Jude Medical, Inc. has announced the European launch of the Unify Quadra cardiac resynchronization therapy defibrillator
Cohera Medical Receives CE Mark Approval for TissuGlu® Surgical Adhesive
Cohera Medical, Inc.®, a rapidly growing medical device company, announced today that it has received CE Mark approval for its lead product, TissuGlu® Surgical Adhesive.
Covidien Announces U.S. 510(k) Clearance and European CE Mark Approval of Parietex(TM) Optimized Composite Mesh
Covidien gains CE mark for its new Parietex Optimized Composite mesh features optimized protection, integration and handling during laparoscopic ventral hernia repair
Covidien Unveils Next Generation EverFlex+(TM) Peripheral Stent System
Covidien has announced availability of the EverFlex+(TM) Self-Expanding Peripheral Stent System in Europe.