Each year, the FDA receives several hundred thousand medical device reports of suspected device-associated deaths, serious injuries and malfunctions. Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products. To learn more about how to report an adverse event, please visit the FDA website for updated information.
FDA is working with U.S. Government partners, including CDC, and international partners to address the coronavirus disease 2019 (COVID-19) outbreak.
FDA is working with U.S. Government partners, including the U.S. Centers for Disease Control and Prevention (CDC), and international partners to closely monitor an outbreak caused by a novel (new) coronavirus first identified in Wuhan City, Hubei Province, China.
The virus has been named “SARS-CoV-2” and the disease it causes has been named “coronavirus disease 2019” (abbreviated “COVID-19”).
While the U.S. Government considers this a serious public health concern, based on current information, the CDC has determined that the immediate health risk from COVID-19 to the general American public is considered low at this time. People in communities where ongoing community spread with the virus that causes COVID-19 has been reported are at elevated risk of exposure. Travelers returning from affected international locations, close contacts of persons with COVID-19, and healthcare workers caring for patients with COVID-19 are at elevated risk of exposure. [Read More]
Each year, SCAI brings together 2,000 physicians, cardiovascular professionals, hospital administrators, academics, and industry professionals from around the world to share knowledge, clinical expertise, and the latest medical advances, with the single goal of advancing care to Save and Enhance Lives.
Date : April 28 – May 1, 2021
Venue: Hyatt Regency, Chicago
One of the best meeting to discuss the M-CATH micro catheter in challenging lesions.
GEST is the premiere global resource for advancing embolotherapy in interventional radiology.
Date: May 14-17, 2020
EKOBI biodegradable microspheres are available in the USA and Canada.
As the largest collection of healthcare product manufacturers and service providers under one roof, FIME is your one-stop shop for all your healthcare sourcing and procurement needs.
FIME 2020 has been cancelled.
Date : summer 2021
Venue: Miami Beach Convention Center, Miami
Dawa Medical LLC will be there to discuss your needs for US Agent, Initial Importer, Distribution and Warehousing.
Transcatheter Cardiovascular Therapeutics (TCT) is the world’s largest and most important educational meeting specializing in interventional cardiovascular medicine. For 32 years, TCT has been the center of cutting-edge educational content, showcasing the latest advances in current therapies and clinical research.
Date : October 14-18, 2020
We were so anxious for that great opportunity to talk about the M-CATH micro catheter for your challenging lesions…next year !
The world of medicine meets at MEDICA 2020. A must of anyone who wants to experience tomorrow’s healthcare market live.
Date : November 16-17, 2020
Venue: Düsseldorf Exhibition Centre, Düsseldorf (Germany)
If you are looking for an Initial Importer for the US market, we will be there to discuss.