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Bleeding Control Articles & Analysis

18 news found

Instylla announces positive results from preclinical studies of Embrace™ Hydrogel Embolic System in hemorrhage models

Instylla announces positive results from preclinical studies of Embrace™ Hydrogel Embolic System in hemorrhage models

Instylla, Inc., a privately held company developing next-generation liquid embolics for peripheral vascular embolotherapy, today announced two publications that evaluated the Embrace™ Hydrogel Embolic System (HES) in preclinical porcine hemorrhage models. In a Journal of Vascular and Interventional Radiology (JVIR) publication, Dr. Gandras et al. evaluated[i] the ability of Embrace HES to ...

ByInstylla, Inc.


The next evolution in blood vessel occlusion

The next evolution in blood vessel occlusion

The good news for his patient was that she was young. A lower extremity bypass procedure - like any surgery - can be more difficult as we age. The bad news was that the best veins for the procedure - which involves grafting a vein from another part of the body to bypass her blocked arteries in the leg - were unusable. The patient had undergone varicose vein treatments as a young woman that ...

ByAmsel Medical Corporation


RevMedx receives CE Mark for XGAUZE® self-expanding gauze.

RevMedx receives CE Mark for XGAUZE® self-expanding gauze.

Manufacturer of the revolutionary XSTAT technology will now have a second sterile wound dressing available in Europe and other International markets. RevMedx, Inc., a global leader in innovative devices that control severe bleeding, today announced it has received CE (Conformité Européenne) Mark Certification for the XGAUZE wound dressing in Europe. XGAUZE, a Class I sterile ...

ByRevMedx


Life-Changing Watchman Procedure for Patient with Kidney Disease

Life-Changing Watchman Procedure for Patient with Kidney Disease

Like many people with atrial fibrillation (AFib), Sheldon Kittelson of Clarkfield, Minnesota, felt trapped between the fear of having a stroke and the fear of spending a lifetime on blood thinners. For people with AFib, blood doesn’t flow through the heart normally, which can result in a clot forming in the left atrial appendage (LAA) that can break loose and lead to a stroke. ...

ByEchoPixel, Inc.


Pfizer and Sangamo Announce Updated Phase 1/2 Results Showing Sustained Bleeding Control in Highest Dose Cohort Through Two Years Following Hemophilia A Gene Therapy

Pfizer and Sangamo Announce Updated Phase 1/2 Results Showing Sustained Bleeding Control in Highest Dose Cohort Through Two Years Following Hemophilia A Gene Therapy

Pfizer Inc. (NYSE: PFE) and Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicines company, today announced updated follow-up data from the Phase 1/2 Alta study of giroctocogene fitelparvovec, an investigational gene therapy for patients with moderately severe to severe hemophilia A. The Alta study data, in patients with severe hemophilia A, are being presented today at the 63rd American ...

BySangamo Therapeutics


Axio Biosolutions receives another FDA clearance for Axiostat Patch for Vascular Bleeding Control

Axio Biosolutions receives another FDA clearance for Axiostat Patch for Vascular Bleeding Control

Axio Biosolutions, an integrated wound care company has announced FDA 510(k) clearance of its hemostatic product, Axiostat Patch that helps control moderate to severe bleeding in vascular procedures, surgical debridement sites, puncture sites and more. Axiostat Hemostatic Patch is based on a protonated bioadhesive technology which works by providing a strong mechanical barrier to the injury ...

ByAxio Biosolutions Pvt Ltd


First Patients Treated in First-in-Human Trial for ACTISEAL – Polyganics’ Innovative Liver and Pancreas Sealant Patch

First Patients Treated in First-in-Human Trial for ACTISEAL – Polyganics’ Innovative Liver and Pancreas Sealant Patch

Polyganics, a medical technology company developing, manufacturing and commercializing bioresorbable medical devices, today announced treatment of the first patients in its first-in-human study for ACTISEAL®, its Liver and Pancreas Sealant Patch. The ‘SHIELDS’ trial is a prospective, multicenter study, evaluating the safety and performance of ACTISEAL® in reducing fluid ...

ByRegenity


Polyganics Awarded €1.2 Million for Clinical Development of Liver and Pancreas Sealant Patch

Polyganics Awarded €1.2 Million for Clinical Development of Liver and Pancreas Sealant Patch

Polyganics, a medical technology company developing, manufacturing and commercializing bioresorbable medical devices, announced today that it has received EUR 1.2 million in funding from the European Fund for Regional Development (EFRO) through the Northern Netherlands Alliance (SNN) and the city and province of Groningen, to support clinical validation of its Liver and Pancreas Sealant Patch. ...

ByRegenity


Grifols reaches revenue of EUR 5,100 million, a 13.6% increase, and raises its profits to EUR 625 million

Grifols reaches revenue of EUR 5,100 million, a 13.6% increase, and raises its profits to EUR 625 million

Revenue increases 13.6% (9.2% cc) as a result of the sustainable growth strategy, with advances in all divisions and regions Bioscience leads the growth with EUR 3,994 million of revenue (13.6%; 8.9% cc). Diagnostic and Hospital continue to make progress with sales of EUR 734 million (4.5%; 1.1% cc) and EUR 134 million (12.5%; 12.1% cc), respectively. Bio Supplies achieves EUR 267 million in ...

ByGrifols International, S.A.


EndoClot Plus, Inc. Announces FDA Clearance of GI Submucosal Lifting Product

EndoClot Plus, Inc. Announces FDA Clearance of GI Submucosal Lifting Product

EndoClot Plus, Inc. (EPI), a privately held medical device company announced the FDA 510(k) clearance of EndoClot® Submucosal Injection Agent (EndoClot® SIA) manufactured by EndoClot Plus Co., Ltd. located in Suzhou, China. This product is expected to be commercially available in the United States beginning in May 2020 and later this year in several international markets. EndoClot® ...

ByEndoClot Plus, Inc.


Gauss Announces Triton Platform Update to Power Maternal Hemorrhage Response

Gauss Announces Triton Platform Update to Power Maternal Hemorrhage Response

Gauss, the leader in AI-enabled surgical applications, announced an over-the-air software update, Triton QBL, that pairs the company’s AI-powered blood loss monitor with integrated protocols and provider alerts that help to synchronize postpartum hemorrhage care. The update will be available to the company’s network of hospital customers this fall. The United States has the highest ...

ByGauss Surgical


Endomedix, Inc. to present its innovative technology addressing the needs of Warfighters at the upcoming Military Health System and Research Symposium 2019 annual meeting

Endomedix, Inc. to present its innovative technology addressing the needs of Warfighters at the upcoming Military Health System and Research Symposium 2019 annual meeting

Endomedix, Inc., today announced that it will present its patented revolutionary technology to control bleeding in battlefield injuries at the upcoming Military Health System and Research Symposium (MHSRS) annual meeting. Loss of blood still remains the most common cause of potentially preventable deaths in battlefield casualties, two-thirds of such deaths result from truncal hemorrhage that ...

ByEndomedix, Inc.


New Publication Concludes Gauss Surgical’s Triton System Associated with Earlier Postpartum Hemorrhage Intervention and Reduced Costs

New Publication Concludes Gauss Surgical’s Triton System Associated with Earlier Postpartum Hemorrhage Intervention and Reduced Costs

Gauss Surgical, a health technology company, announced that a new study published in the International Journal of Obstetric Anesthesia concluded that the use of the company’s Triton system to monitor maternal blood loss during labor and delivery was associated with earlier postpartum hemorrhage intervention and cost savings. Researchers at Mount Sinai Hospital (New York, NY) studied over ...

ByGauss Surgical


TX Series added to CoTCCC list of recommended limb tourniquets

TX Series added to CoTCCC list of recommended limb tourniquets

RevMedx, Inc., a leader in groundbreaking solutions for the control of severe bleeding, today announced that the CoTCCC has added the TX Series ratcheting tourniquets to its list of recommended Limb Tourniquets. The TX series joins the XSTAT® injectable hemostatic on the TCCC list of recommended hemorrhage control devices for casualty care. Andrew Barofsky, President and CEO of RevMedx, ...

ByRevMedx


EndoClot Expands GI Hemostasis Portfolio With Launch of EndoClot® Adhesive

EndoClot Expands GI Hemostasis Portfolio With Launch of EndoClot® Adhesive

EndoClot Plus, Inc., a privately held medical device company founded by surgeons and biomaterial scientists announces the CE approval of EndoClot® Adhesive manufactured by EndoClot Plus Co., Ltd. located in Suzhou, China. The product will be made available for discussion during the upcoming Digestive Disease Week held in Washington DC, June 2-5, 2018. EndoClot® Adhesive is a single-use ...

ByEndoClot Plus, Inc.


RevMedx receives CE Mark for XSTAT® injectable hemostatic devices

RevMedx receives CE Mark for XSTAT® injectable hemostatic devices

Revolutionary bleeding control technology will now be available in Europe and other International markets. RevMedx, Inc., a leader in innovative devices that control severe bleeding, today announced it has received CE (Conformité Européenne) Mark Certification for the XSTAT 30 and XSTAT 12 hemostatic devices in Europe. Unlike traditional wound treatments that may take several ...

ByRevMedx


Medtech Startup Poised for Success

Medtech Startup Poised for Success

Medtech startup Endomedix is feeling the excitement and satisfaction that follows five years of hard work, and the company is poised for its next key stage of growth. Led by CEO Richard Russo, a veteran at developing products and building businesses, Endomedix has overcome many of the challenges and early missteps that overwhelm most medical device startups. Russo came to Endomedix in 2009 after ...

ByEndomedix, Inc.


Russo finds NJIT is the place to be for Endomedix

Russo finds NJIT is the place to be for Endomedix

Four years ago, Endomedix CEO Richard Russo recognized Stony Brook University was not meeting his company’s needs when it came to facilities and experienced professors. So he loaded up and moved down to the New Jersey Institute of Technology. By relocating to the Newark-based university, the company has been able to tap into the institution’s human and financial resources, allowing ...

ByEndomedix, Inc.

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