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Intra Aortic Balloon Pump

intra aortic balloon pump membersMembers related to intra aortic balloon pump

 
Dave1981 California
I am healthcare professional with qualifications in medicine, nutrition and physical... More
IowaGirlEats West Des Moines, Iowa
I’ve lived in Iowa for the better part of 26 years (minus a three year stint in... More
carlp California
i am 62and have been a diabetic for 30 years insulin dependant for about 15years i have been in... More
Ruth Maputo, MZ
David J. Hillsborough, California
I love to do anything that gets the adrenaline pumping

intra aortic balloon pump Blogs and DiscussionsArticles

 
Maquet Datascope Corp. Intra-Aortic Balloon Pumps: Recall – Shuts Off Without Warning by FDA already-present ischemia, thrombus formation, organ injury or other serious events.  BACKGROUND: The intra-aortic balloon pump is an electromechanical system used to inflate and deflate an intra-aortic balloon to provide...
Voluntary Worldwide Field Correction Issued for the S98/98XT, CS100/CS100i and CS300 Intra-Aortic Balloon Pumps by FDA a voluntary worldwide field correction of certain Intra-Aortic Balloon Pumps (IABPs) sold under the Datascope..., CS100/CS100i and CS300 Intra-Aortic Balloon Pumps (IABPs) sold under the Datascope Corp. System 98/98XT...
Class I Medical Device Recall: Arrow Ultra 8 Intra-Aortic Balloon Catheters (IABS) 8 FR 30CC and 40CC Universal and Arrow Intra- by FDA Products: Arrow IAB (Intra Aortic Balloon), Ultra 8 Fr, 30cc Arrow IAB (Intra Aortic Balloon), Ultra 8 Fr, 40cc Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and a Measurement System...
Arrow Intra-Aortic Balloon (IAB) Catheter Products: Class 1 Recall - Catheters Can Become Stuck in the Sheath by FDA Ultra 8 Intra-Aortic Balloon Catheters (IABS) 8 FR 30CC and 40CC Universal and Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and a Measurement System are recalled...
Federal Register: Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary by FDA The FDA is issuing a proposed administrative order to reclassify intra-aortic balloon and control system devices when indicated for acute coronary syndrome, cardiac and non-cardiac surgery, or
Federal Register: Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems for Acute Coronary Syndro by FDA The FDA is issuing a final order to reclassify intra-aortic balloon and control system (IABP) devices when indicated for acute coronary syndrome, cardiac and non-cardiac surgery, or complications
The World’s Smallest Heart Pump Saving Lives in the US - Impella by Medical Quack Patient ExpertHealth Maven One official stated that this device stands to replace the intra-aortic balloon pump... in Texas and the newsman covering the story with one in his hand showing the power of the pump submerged...
Cook Medical Announces FDA Clearance for Advance® 35LP PTA Balloon Dilatation Catheter - PVD by Medical Quack Patient ExpertHealth Maven in the legs are a bit more complex.  Aside from pumping the heart is stationary, whereas the legs... of low-profile PTA balloons, provides physicians with enhanced deliverability to the superficial femoral...
PMA Final Decisions for June 2011 by FDA 6/13/11 135-Day GYNECARE THERMACHOICE III Uterine Balloon Therapy System ETHICON, Inc. Somerville, NJ 08876 Approval for changes to the catheter balloon...
PMA Final Decisions for August 2011 by FDA . P860004/S156 8/17/11 SynchroMed II Implantable Infusion Pump/Intra-arterial Vascular... Pump Medtronic Neuromodulation Minneapolis, MN 55432 Approval for labeling...

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