| 881 - 900 of 1000 Benin Republic News Headlines |
Page 45 of 50 Pages |
ST. JUDE MEDICAL ANNOUNCES AGREEMENT WITH LUMEDX TO MANAGE CARDIOVASCULAR PATIENT DATA
FDAnews
- Sunday, August 13, 2006
St. Jude Medical, Inc. today announced a joint marketing and development agreement with LUMEDX to integrate and manage cardiovascular patient
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AMERICAN MEDICAL SYSTEMS SIGNS CROSS-LICENSING AGREEMENT WITH CALDERA MEDICAL
FDAnews
- Sunday, August 13, 2006
American Medical Systems Holdings, Inc. and Caldera Medical, Inc. today announced that they have entered into a settlement and cross-license
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TOPSPIN MEDICAL GETS FDA APPROVAL TO START CLINICAL TRIALS IN THE US AND COMPLETES THE DEVELOPMENT OF A PROTOTYPE OF ITS ADVANCED GENERATION INTRAVASCULAR MRI (IVMRI) CATHETER
FDAnews
- Sunday, August 13, 2006
TopSpin Medical announced it has received FDA approval to start conducting clinical trials in the US with its IntraVascular MRI (IVMRI) catheter, intended for the characterization of lipid-rich lesions in the coronary
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rison Inmates 'Like Corpses in the Drawers of a Morgue'
allAfrica.com
- Sunday, August 13, 2006
Maggots usually digest the bodies of the dead. In Benin's cramped and decaying prison of Abomey they infest the flesh of the
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Ministry Warns Illegal Land Speculators
allAfrica.com
- Sunday, August 13, 2006
Federal Ministry of Housing and Urban Development has warned land speculators in Benin City who have been selling land belonging to the Federal Government illegally to desist from doing so or be prepared to face the wrath of the government. Besides, it said that all illegal structure or property developed
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Benin Receives Assistance for Forests, Adjacent Lands Management Program
allAfrica.com
- Sunday, August 13, 2006
The World Bank Board of Executive Directors today approved a project that will promote socially, technically and economically viable management of forest and adjacent land resources by communities in
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PPEALS COURT CALLS STATE DME MEDICAID POLICY 'UNREASONABLE'
FDAnews
- Sunday, August 13, 2006
A panel of the Eighth U.S. Circuit Court of Appeals June 22 overturned a ruling in a case where a Missouri policy denied Medicaid device coverage to most of the state's adult program
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MRL, FDA ANNOUNCE CLASS I RECALL FOR ANOTHER BRAND OF WELCH ALLYN AEDS
FDAnews
- Sunday, August 13, 2006
MRL has issued a worldwide Class I recall of 1,184 Welch Allyn PIC50 automated external defibrillators (AEDs) manufactured between February 2002 and October 2004, the FDA said July
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PLAINTIFF WINS CASE AGAINST J&J, ALZA FOR TRANSDERMAL PATCH DEFECT
FDAnews
- Sunday, August 13, 2006
A Houston jury July 7 awarded $772,500 to the daughter of a woman who died in 2004 after using a fentanyl transdermal drug patch sold by Johnson & Johnson
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FDA APPROVES CLINICAL TRIAL FOR MEDTRONIC'S DIAM SPINAL STABILIZATION SYSTEM
FDAnews
- Sunday, August 13, 2006
Medtronic, Inc. announced today that the U.S. Food and Drug Administration (FDA) has granted an investigational device exemption (IDE) to the DIAM Spinal Stabilization System for use in a clinical
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PROMETHEUS LAUNCHES PROMETHEUS IBD SEROLOGY 7
FDAnews
- Sunday, August 13, 2006
Prometheus Laboratories Inc., a specialty pharmaceutical company announced today that it has launched PROMETHEUS IBD Serology 7, the Company's most advanced diagnostic panel for inflammatory bowel
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INTERTON SELECTS AMI SEMICONDUCTOR FOR DEVELOPMENT OF ADVANCED WIRELESS CAPABILITIES IN DIGITAL HEARING AIDS
FDAnews
- Sunday, August 13, 2006
AMI Semiconductor, a designer and manufacturer of state-of-the-art integrated mixed-signal and structured digital products, today announced that it has been selected by Interton, a leading hearing system manufacturer, to develop advanced wireless capabilities in hearing aid devices through an ultra low-power radio frequency (RF)
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EUROCOR GMBH RECEIVES CE MARK APPROVAL FOR TAXCOR I
FDAnews
- Sunday, August 13, 2006
Eurocor Gmbh an Opto Circuits company has received CE mark approval of its new polymer-free, TAXCOR I.Paclitaxel-eluting coronary stent
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NORTHSTAR NEUROSCIENCE SELECTS AMI SEMICONDUCTOR TO DEVELOP ASIC FOR NEW STROKE THERAPY NEUROSTIMULATION DEVICE
FDAnews
- Sunday, August 13, 2006
AMI Semiconductor, a leading designer and manufacturer of state-of-the-art integrated mixed-signal and structured digital products for the automotive, medical and industrial markets, today announced that Northstar Neuroscience, Inc., a medical device company, selected AMIS to design and manufacture the application specific integrated circuit (ASIC) for the Northstar Stroke Recovery
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NC IDEA GRANTS AWARDED TO SEVEN N.C. COMPANIES
FDAnews
- Sunday, August 13, 2006
NC IDEA has awarded $225,000 in grants to seven early-stage companies located throughout North Carolina ? CardioVascular Resonances, Illuminus, InsituTec, ZumaTek, DeltaSphere, ImagineOptix, and
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World Bank President Travels to Africa On the Eve of the G8 Summit
allAfrica.com
- Sunday, August 13, 2006
World Bank President Paul Wolfowitz began today the first of two visits to Africa this month, before and after the G8 summit, where he will press world leaders to make good on the pledges they made last year to help Africa's poorest
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GERMAN-BASED EKSA CITED FOR QS, MDR VIOLATIONS
FDAnews
- Sunday, August 13, 2006
ESKA Implants was issued a May 16 warning letter for quality system (QS) and medical device reporting deficiencies that were uncovered during a November 2005 inspection of the company's Lubeck, Germany,
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MINIMALLY INVASIVE DEVICE MARKET SHOULD SEE BIG GROWTH, ANALYST SAYS
FDAnews
- Sunday, August 13, 2006
The global market for minimally invasive surgery (MIS) devices and instruments ? including catheters, balloons, stents and other devices used in minimally invasive angioplasty ? is expected to grow from an estimated $12 billion in 2005 to $12.9 billion in 2006 and should reach $18.5 billion by 2011, according to
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FDA CLEARS BIOSITE DRUG SCREENING DIAGNOSTIC TO PERFORM METHADONE DETECTION
FDAnews
- Sunday, August 13, 2006
Biosite has received FDA clearance to its Triage TOX Drug Screen diagnostic test for methadone detection, the company said July
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BOSTON SCIENTIFIC LAUNCHES RADIAL JAW 4, NEWEST VERSION OF SINGLE-USE BIOPSY FORCEPS
FDAnews
- Sunday, August 13, 2006
Boston Scientific Corporation announced the U.S. launch of the newest version of its Radial Jaw Single-Use Biopsy Forceps, featuring more jaw volume and an improved jaw design compared to the market-leading Radial Jaw 3
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