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Automated External Defibrillators For Sale - Articles

Cardiac Science Partners with Best Buy Geek Squad And/Or IT Experts For Sales, Tech Support and Consulting To Include Medical R by Medical Quack Patient ExpertHealth Maven Posted Thu 22 Jul 2010 7:48pm Well it looks like electronic medical records support has reached the retail level.  The article is not too specific on exactly which services they will be supporting but I might guess the medical records part of the business, HeartCentrix might be right in there as it will communicate with various devices that record and collect data and tra ... Read on »
Cardiac Rhythm Management Devices World Markets --- Aarkstore Enterprise by aarks222 Posted Thu 18 Nov 2010 11:19am This TriMark Publications report reviews the worldwide cardiac rhythm management market size for the U.S., European and Asian markets. Individual country markets such as Japan, the Philippines, Australia, and the Middle East are covered. Important regulatory issues that impact the use of cardiac rhythm devices are explored for countries like ... Read on »
Cell Therapy Markets --- Aarkstore Enterprise by aarks222 Posted Thu 18 Nov 2010 11:30am This TriMark Publications report reviews the worldwide cardiac rhythm management market size for the U.S., European and Asian markets. Individual country markets such as Japan, the Philippines, Australia, and the Middle East are covered. Important regulatory issues that impact the use of cardiac rhythm devices are explored for countries like ... Read on »
FDA issues proposal to improve the quality of automated external defibrillators by FDA Posted Fri 22 Mar 2013 12:00am The U.S. Food and Drug Administration today issued a proposed order aimed at helping manufacturers improve the quality and reliability of automated external defibrillators (AEDs). Read on »
Defibtech Lifeline and ReviveR Automated External Defibrillators (AEDs): Recall - Software Defect May Cancel Shock by FDA Posted Wed 11 May 2011 8:00am [Posted 05/10/2011] AUDIENCE: Emergency Medicine, Risk Manager ISSUE: Devices subject to this recall include Model DDU-100 series with software version 2.004 or earlier, sold under the brand names Lifeline and ReviveR. AEDs using software version 2.004 or earlier may cause the device to cancel shock during the charg ... Read on »
Philips HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite Automated External Defibrillators (AED) by FDA Posted Tue 03 Dec 2013 12:00am In September 2012, Philips Healthcare initiated a Voluntary Medical Device Recall of HeartStart Frx, HeartStart HS1 Home, and HeartStart HS1 OnSite AEDs after determining that an internal electrical component in the AED could fail, and the device could... Read on »
FDA Says Build a Better External Defibrillator And Starts a Program-Too Many Recalls by Medical Quack Patient ExpertHealth Maven Posted Tue 16 Nov 2010 2:30am The FDA has begun an extensive look at the design and use of the devices.  According to this article there have been too many mishaps and the FDA believes better designs with incorporating new technologies would improve the process by working with the manufacturers.  In addition the FDA stated they would look at current products on the market ... Read on »
External Defibrillators Not Much Help in Hospitals by Medline Plus Posted Mon 15 Nov 2010 12:00pm While effective in public places, study found differently in hospital setting Monday, November 15, 2010 MONDAY, Nov. 15 (HealthDay News) -- Although automated external defibrillators have been found to reduce heart attack death rates in public places such as restaurants, malls and airplanes, they have no ... Read on »
FDA Launches Initiative to Develop Innovative External Defibrillators by Medline Plus Posted Mon 15 Nov 2010 7:05pm FDA NEWS RELEASE For Immediate Release: Nov. 15, 2010 Media Inquiries: Dick Thompson, 301-796-7566, Dick.Thompson@fda.hhs.gov Consumer Inquiries: 888-INFO-FDA   FDA launches initiative to develop innovative external defibrillators Safety concerns on the devices that treat abnormal heart rhythms also to be address ... Read on »
Medtronic to Recall External Defibrillators by Medical Quack Patient ExpertHealth Maven Posted Thu 22 Apr 2010 8:55pm The FDA has stated it is a Class 1, the most serious type.  To repair the devices the company will be sending service personnel out to fix the units.  These are not consumer units but rather ones used in hospitals or by paramedics.  A unit of Medtronic said Thursday that federal regulators have determined a type of external defibrillator ... Read on »