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International

Devon Medical Products Announces Strategic Alliance with PKUcare BeiYi Pharmaceutical Co. to Distribute U.S.-Made Medical Products in China

May 18 | News

Devon Medical Products, a global medical device manufacturer and distributor, today announced PKUcare BeiYi Pharmaceutical Co. (PKU) as a strategic distribution partner in the People’s Republic of China. Under the agreement, PKU will distribute...

Think that Europe is more welcoming to medical devices? It may not be for long

May 4 | News

The grass is greener on the other side. That is traditionally how device makers have viewed Europe when it comes to medical device regulation and the ease of getting products approved and commercialized compared to the U.S.

US spends far more for health care than 12 industrialized nations, but quality varies

May 4 | News

The United States spends more on health care than 12 other industrialized countries yet does not provide "notably superior" care, according to a new study from The Commonwealth Fund. The U.S. spent nearly $8,000 per person in 2009 on health care services...

Indian Prime Minister Inaugurates Elekta Cancer Treatment Machine at Bhubaneswar Borooah Cancer Institute

May 2 | News

Prime Minister of India, Dr. Manmohan Singh, honored Bhubaneswar Borooah Cancer Institute by presiding over the inauguration of its Elekta Synergy linear accelerator on April 20 in Guwahati. The Synergy system – equipped to perform the most advanced radiotherapy...

Elekta's New Agility MLC Solution Poised to Revolutionize Beam Shaping of Radiation Therapy Cancer Treatments

Apr 2 | News

CRAWLEY, England/PRNewswire/ -- Elekta announced today it has received clearance to CE mark Agility™*, a revolutionary beam-shaping device integrated into the head of a linear accelerator (linac). Patients and clinics will benefit from the speed and reliability of this new MLC design.

Diabetes Set to Become Biggest Killer in India, China and Brazil

Mar 22 | News

NEW YORK (GBI Research) - The emerging countries of India, Brazil and China are seeing swift increases in the prevalence of diabetes, as financial development is met by unhealthy lifestyle choices and subsequent chronic disease, according to a new report by business intelligence expert GBI Research.

Interventional Cardiology Device Markets in Pakistan, Saudi Arabia, South Africa and Turkey to Grow to $461 Million by 2016

Mar 13 | News

TORONTO--(BUSINESS WIRE)--According to Millennium Research Group (MRG), the global authority on medical technology market intelligence, the interventional cardiology (IC) market in Pakistan, Saudi Arabia, South Africa and Turkey will reach a value of more than $460 million by 2016.

MEDICREA’s PASS MIS: FDA Approval and First Surgery in the US

Feb 9 | News

LYON, France--(BUSINESS WIRE)--The MEDICREA group, a medical company specialized in the development of innovative surgical technologies for the treatment of spinal pathologies, today announced the approval by the FDA of the PASS MIS system and the first PASS MIS surgery...

Tornier to Highlight Products and Education Programs at American Academy of Orthopedic Surgeons (AAOS) Meeting

Feb 9 | News

AMSTERDAM--(BUSINESS WIRE)--Tornier N.V., a global medical device company focused on providing surgical solutions to orthopaedic extremity specialists, today announced it will highlight a range of products and patient education programs at the American Academy of Orthopaedic Surgeons...

UroShield Applied to Urinary Catheters Increases Susceptibility of Bacteria Biofilm to Antibiotic Treatment

Feb 9 | News

NESHER, Israel--(BUSINESS WIRE)--NanoVibronix, a medical device company which develops innovative therapeutic ultrasound applications, reported that a study titled “Surface Acoustic Waves Increase the Susceptibility of Pseudomonas Aeruginosa Biofilms to Antibiotic Treatment” has been published...

BD Veritor System for Flu A+B Featuring Alverix Technology Receives Regulatory Approval in Japan

Feb 9 | News

SAN JOSE, Calif.--(BUSINESS WIRE)--Alverix announced today that BD (Becton, Dickinson and Company) has received approval from the Japanese Ministry of Health, Labour, and Welfare (MHLW) for the BD Veritor™ System Flu A+B Test. The BD Veritor System was developed...

Which Way to Go: CE Mark or FDA Approval?

Feb 7 | Articles

Start-ups and large device makers alike have difficulty bringing new products to market without greater predictability and transparency from the FDA. According to an online survey funded by the medical technology industry’s Institute for Health Technology Studies, most medical device companies today are seeking regulatory approval and launching their products overseas first. This article will look at whether this is a good business decision for all device manufacturers.

Genetic variant increases risk of common type stroke

Feb 5 | News

(Wellcome Trust) A genetic variant that increases the risk of a common type of stroke has been identified by scientists in a study published online in Nature Genetics today. This is one of the few genetic variants to date to be associated with risk of stroke and the discovery opens...

Irish Medical Device Association: Vibrant Med Tech Sector in Ireland Identifies Continued Evolution & Convergence in 4 Year Plan

Feb 2 | News

DUBLIN--(BUSINESS WIRE)--Over the last twelve months, medical technology companies publically announced the investment of approximately €170m and the creation of an estimated 875 jobs in Ireland over the coming years, according to the Irish Medical Device Association (IMDA)...

Cook Medical Launches Zenith Low Profile Endovascular Graft in Canada

Feb 1 | News

Stouffville, Ontario—Following Health Canada approval, the Zenith Low Profile AAA Endovascular Graft (Zenith AAA LP) from Cook Medical is now approved and will be launched to physicians in Canada. With a low-profile delivery system diameter of 18 Fr and simplified deployment...

Singapore Scientists Lead in 3D Mapping of Human Genome to Help Understand Human Diseases

Feb 1 | News

Singapore - (ACN Newswire) - Genome Institute of Singapore's (GIS) Associate Director of Genomic Technologies, Dr Yijun RUAN, led a continuing study on the human genome spatial/structural configuration, revealing how genes interact/communicate and influence each other, even when...

Baxter Announces FDA Approval of Expanded Indication for TISSEEL [Fibrin Sealant] for General Hemostasis in Surgery

Jan 31 | News

DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. announced today that the U.S. Food and Drug Administration (FDA) has approved TISSEEL [Fibrin Sealant] to include general hemostasis in surgery when control of bleeding by standard surgical techniques is ineffective or impractical.

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