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SafeBreak Vascular is a break-away connector that fits into any peripheral IV line in the world. The device is designed to separate when damaging force is placed on an IV line, reducing vein irritation and the chances of the IV dislodging. When the device se
The FDA on March 21 shared recommendations for healthcare organizations to conserve prefilled 0.9 percent sodium chloride intravenous lock/flush syringes amid a national shortage.
1. Use preservative-free, sterile 0.9 percent sodium chloride single dose vials if the prefilled syrin
The Medical Device Business Journal — Medical Device News & Articles | MassDevice
The on-label, prospective, multi-center study showed meaningful relief using DTM SCS endurance therapy, a modified, lower-energy variation of Medtronic’s Differential Target Multiplexed (DTM) SC
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The products discussed here were indep
February 11th, 2022 Coherent Market Insights Releases
Implementation of lockdown across various countries because of pandemic has put an economic burden on the private healthcare sector. Medical service providers are facing shortage of raw m
February 8th, 2022 Coherent Market Insights Releases
On May 23, 2020 the Centres for Disease Control and Prevention released an updated interim additional guideline to prevent the infection spread in outpatient hemodialysis facilities. Some
February 11th, 2022 DelveInsight Business Research Releases
The Catheter Stabilization/Securement Device market is anticipated to grow at a CAGR of 6.34% and will rise upto USD 1.88 billion by 2026, as per DelveInsight.
The Global
(May 26, 2015) VertiFlex, Inc., announced that it has been granted pre-market approval by the FDA for its minimally invasive treatment of lumbar spinal stenosis, the Superion Interspinous Spacer System. This approval comes after a successful 470 patient IDE study of the Superion
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