A new micro diaphragm pump from the Precision Fluidics Division of Parker Hannifin Corporation is specifically designed for the needs of portable medical devices for advanced wound care. The Parker T2-05-IC micro diaphragm pump provides ...
Tags: Micro Diaphragm Pump, Pump
US-based OrthoSensor has announced its plans to launch its Verasense knee system in European markets after recently receiving CE Mark approval. US-based OrthoSensor has announced its plans to launch its Verasense knee system in European ...
Tags: Verasense Knee System
Bausch + Lomb Technolas, a US-based eye care company, has obtained the CE mark for its Technolas Teneo 317 excimer laser workstation, which is designed to treat all types of ametropia (refractive errors). In addition to traditional LASIK ...
Shanghai MicroPort EP MedTech, a wholly-owned subsidiary of Shanghai MicroPort Medical Group, has obtained CE Mark approval for its Columbus 3D EP navigation system, indicated for the diagnosis and treatment of complex arrhythmia diseases. ...
Sequenom, a US-based manufacturer of DNA massarrays, has announced the submission of premarket 510(k) notifications to the US Food and Drug Administration (FDA) for its IMPACT Dx system and the IMPACT Dx Factor V Leiden and Factor II ...
Tags: Impact DX System, Sequenom
Medtronic, a US-based medical device manufacturer, has obtained the CE Mark and announced the launch of its new cervical cage system called Compact Cornerstone-SR Alliance. Compact Cornerstone-SR Alliance cage system has been designed to ...
Tags: Medtronic, Cervical Cage System
SEMI-GAS Systems, a division of Applied Energy Systems Inc of Malvern, PA, USA and a manufacturer of ultra-high-purity gas source and distribution systems, has launched an Xturion custom gas source system that safely and continuously ...
Tags: SEMI-GAS Gas delivery systems, Electrical, Electronics
Smart Vision Lights, a leader in LED research and development, engineering, and manufacturing of machine vision lights for the advanced lighting industry, was recently qualified as a Level IV LED testing and certification facility by ...
Cardiovascular device company CardioLogical Solutions has obtained two additional patents for its family of aortic embolic protection devices, developed to prevent stroke and other ischemic complications. The first patent is issued for ...
Actuated Medical, a US-based medical device company, has obtained the additional US Food and Drug Administration (FDA) approval for its TubeClear system. The company has added several new clearing stem models for the TubeClear system and ...
Tags: Actuated Medical, medical device
US-based in vitro diagnostic company Venaxis announced that the Data and Safety Monitoring Board (DSMD) has recommended the continuation of pivotal clinical trial of the APPY1 test, a multiple biomarker-based assay for identifying patients ...
Tags: Appy1 Test, Clinical Trial
Medtronic, a US-based manufacturer of implantable heart-rhythm devices, has obtained the US Food and Drug Administration (FDA) approval for the Complete SE (self-expanding) vascular stent for use in superficial femoral artery (SFA) and ...
Tags: Medtronic, Lower Extremities
Luminex, a biotechnology company, has obtained the US Food and Drug Administration (FDA) and European approvals for a new personalized medicine genotyping assay, xTAG CYP2C19 kit. xTAG CYP2C19 kit is a comprehensive genotyping assay that ...
Tags: Genotyping Assay, Luminex
US-based LabStyle Innovations has obtained CE Mark approval for its Dario smartphone-based glucose monitor and comprehensive diabetes management system. Particularly useful for insulin-dependent patients, the system provides patients, ...
US-based Sapheon has submitted the first module of pre-market approval (PMA) application to the US Food and Drug Administration (FDA) for its VenaSeal sapheon closure system, designed to treat venous reflux (varicose veins) disease. This ...
Tags: PMA Application, Medicine