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The Medical Industry
Business Weekly
May 08, 2008

Other Headlines

DOTmed was first to break the news late last week that GE's OEC division was given the green light to re-start production; GE says more than 300 OEC® 9900 Elite C-arms are slated to ship within the first 10 days as they start to fill back-orders.
Quinn succeeds Jim Reid-Anderson, who has been named new CEO of Siemens Healthcare.
Account rep Grant Norris is DOTmed Certified.
Normally, three's a crowd. But the trifecta of OEMs, refurbishers and broker/dealers is the engine that's driving the medical trailer business.
Online marketplace for new and used medical equipment reaches another milestone.

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More Industry Headlines

OEC Re-Certified by FDA -- Latest Update DOTmed was first to break the news late last week that GE's OEC division was given the green light to re-start production; GE says more than 300 OEC® 9900 Elite C-arms are slated to ship within the first 10 days as they start to fill back-orders.

SNM Annual Meeting Just About a Month Away The Society of Nuclear Medicine -- SNM -- holds its Annual Meeting this June 14-18 in New Orleans, LA. Exhibitors: You can still get a booth if you hurry!

Medicare Expands Coverage for Artificial Heart Devices Decision opens access to advanced technology.

GE Healthcare Introduces New 3.0T MR Scanner Breakthrough technology with simple design provides radiologists with powerful applications for increased clinical capability.

Get Your Bid in Now on This GE Signa MR/i Hispeed Plus MRI Scanner -- Just Posted on DOTmed! Also see the other great lasers, imaging systems, and more... all on your favorite website for used medical equipment!

Manufacturer of Heart Defibrillator Signs Consent Decree of Permanent Injunction Device manufacturer Physio-Control, Inc., its parent company Medtronic, Inc., and their two top executives have signed a consent decree of permanent injunction related to Automatic External Defibrillators.

Legislative Work Continues on Revamping FDA Congress, Agency say more funding is needed to improve safety.

Cosmetic Soft-Tissue Filler Injections Linked to Cases of Acute Renal Failure Investigation finds adverse effects from non-medically supervised procedures.

Wolters Kluwer Health & Johns Hopkins Launch The Patient First journal dedicated to using scientific methods for patient-centric research.

Speaker to Explore Amazing Future of Biotechnology at AAMI Conference Joint Commission executive to provide up-to-date guidance at Association for the Advancement of Medical Instrumentation meeting May 31-June 2 in San Jose, CA.

The 2008 MDMA Annual
Meeting is June 12-13
in Washington, DC

Healthcare Experts to Address Medical Technology Executives at Annual Conference

by Becky Jacoby, Reporter
Medical device industry leaders and key healthcare subject matter experts will meet in Washington, DC for the 2008 Annual Meeting of the Medical Device Manufacturers Association (MDMA). The conference will be held June 12th and 13th at the Marriott, Metro Center.

As the voice for innovative, entrepreneurial medical technology companies, MDMA brings lawmakers and industry executives together annually to confer about the potential impact of developments in industry and government. Panelists will discuss topics in the areas of patents, the health care system, reimbursement issues, international markets, and legal compliance.

"The meeting provides industry leaders with the opportunity to network with colleagues and hear from lawmakers and leading government officials about current and future trends in our industry," said Joe Kiani, Chairman and CEO of Masimo Corporation.

The MDMA is a national trade organization based in Washington, DC. It seeks to improve the quality of patient care by providing marketplace opportunities for innovative products and new medical technology. To find out more, call MDMA at (202) 354-7172, or visit www.medicaldevices.org.

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