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In a study conducted by a Northeast hospital, Pressure Right, a new 5" medical-style, acupressure wristband, was found to help reduce the incidence of postoperative nausea and vomiting (PONV) to a very low level in high-risk patients.
Medical Carbon Research Institute L.L.C. (MCRI(TM)) announced initiation of the FDA approved clinical trial PROACT (Prospective Randomized On-X(R) Prosthetic Heart Valve Anticoagulation Clinical Trial) being conducted under an investigational device exemption (IDE) at reduced anticoagulation levels at Emory Crawford Long Hospital, Emory University in Atlanta, Georgia.
Nanomaterials group Oxonica jumped on news it has signed a licence agreement for its Nanoplex technology with US medical technology firm Becton, Dickinson and Company (BD).
Possis Medical, Inc., announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its GuardDOG Occlusion System for use during the treatment of peripheral vascular disease.
Centers for Medicare & Medicaid Services (CMS) proposals to cut physician fee schedules could lead doctors to severely scale back on new device purchases.
Irish industry is in the grip of an energy crisis and the forthcoming Budget must address fiscal imbalances in the cost of energy and the loss of competitiveness due to rising oil prices, according to the Irish Medical Devices Association (IMDA).
Emergency Filtration Products Inc. reported that its NanoMask has been registered with the Therapeutics Goods Administration (TGA) (the Australian counterpart to the U.S. FDA) as a Class 1 medical device.