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	<title>Diagnostics Product Guide</title>
	<atom:link href="http://blog.diagnosticsproductguide.com/feed/" rel="self" type="application/rss+xml" />
	<link>http://blog.diagnosticsproductguide.com</link>
	<description>A comprehensive guide to cardiology products for medical professionals </description>
	<lastBuildDate>Wed, 29 Sep 2010 11:14:50 +0000</lastBuildDate>
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		<title>Research Demonstrates Progress Towards DNA Strand Sequencing</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/29/research-demonstrates-progress-towards-dna-strand-sequencing/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/29/research-demonstrates-progress-towards-dna-strand-sequencing/#comments</comments>
		<pubDate>Wed, 29 Sep 2010 11:14:50 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Genetic Testing]]></category>
		<category><![CDATA[alpha hemolysin]]></category>
		<category><![CDATA[DNA]]></category>
		<category><![CDATA[enzyme]]></category>
		<category><![CDATA[Nature Nanotechnology]]></category>
		<category><![CDATA[protein nanopore]]></category>
		<category><![CDATA[Research]]></category>
		<category><![CDATA[University of California Santa Cruz]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=371</guid>
		<description><![CDATA[Research published this week in Nature Nanotechnology shows a new method of enzyme-controlled movement of a single strand of DNA through a protein nanopore. The paper, by researchers at the University of California Santa Cruz (UCSC), represents a key step towards nanopore sequencing of DNA strands. The publication describes the observation of single stranded DNA [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-372" href="http://www.diagnosticsproductguide.com/blog/2010/09/29/research-demonstrates-progress-towards-dna-strand-sequencing/university-of-california-santa-cruz/"><img class="alignleft size-full wp-image-372" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/University-of-California-Santa-Cruz3.png" border="0" alt="University of California Santa Cruz" width="200" height="56" /></a>Research published this week in Nature Nanotechnology shows a new method of enzyme-controlled movement of a single strand of DNA through a protein nanopore. The paper, by researchers at the University of California Santa Cruz (UCSC), represents a key step towards nanopore sequencing of DNA strands. The publication describes the observation of single stranded DNA (ssDNA) as it translocates through a protein nanopore, alpha hemolysin (AHL).</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/202707.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/29/research-demonstrates-progress-towards-dna-strand-sequencing/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Angiotech Announces Long-Term Data Show Advantages For Taxus(R) Liberté(R) Stent In Small Vessels And Long Lesions</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/29/angiotech-announces-long-term-data-show-advantages-for-taxusr-liberter-stent-in-small-vessels-and-long-lesions/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/29/angiotech-announces-long-term-data-show-advantages-for-taxusr-liberter-stent-in-small-vessels-and-long-lesions/#comments</comments>
		<pubDate>Wed, 29 Sep 2010 11:08:51 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Cardiology]]></category>
		<category><![CDATA[Angiotech Pharmaceuticals]]></category>
		<category><![CDATA[Boston Scientific Corporation]]></category>
		<category><![CDATA[clinical program]]></category>
		<category><![CDATA[elute]]></category>
		<category><![CDATA[Liberté®]]></category>
		<category><![CDATA[Paclitaxel-Eluting Stent System]]></category>
		<category><![CDATA[TAXUS ATLAS]]></category>
		<category><![CDATA[TAXUS®]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=367</guid>
		<description><![CDATA[Angiotech Pharmaceuticals, Inc. announced that its corporate partner, Boston Scientific Corporation, has released comprehensive data from the TAXUS ATLAS clinical program, a series of global, prospective, singlearm trials evaluating the TAXUS® Liberté® Paclitaxel-Eluting Stent System in a variety of lesions and patient groups. Five-year results from the TAXUS ATLAS trial and four-year results from the [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-368" href="http://www.diagnosticsproductguide.com/blog/2010/09/29/angiotech-announces-long-term-data-show-advantages-for-taxusr-liberter-stent-in-small-vessels-and-long-lesions/angiotech-pharmaceuticals/"><img class="alignright size-full wp-image-368" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/Angiotech-Pharmaceuticals1.png" border="0" alt="Angiotech Pharmaceuticals" width="200" height="79" /></a>Angiotech Pharmaceuticals, Inc. announced that its corporate partner, Boston Scientific Corporation, has released comprehensive data from the TAXUS ATLAS clinical program, a series of global, prospective, singlearm trials evaluating the TAXUS® Liberté® Paclitaxel-Eluting Stent System in a variety of lesions and patient groups. Five-year results from the TAXUS ATLAS trial and four-year results from the TAXUS ATLAS Small Vessel and Long Lesion trials continue to show significant advantages for the thin-strut TAXUS Liberté Stent.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/202521.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/29/angiotech-announces-long-term-data-show-advantages-for-taxusr-liberter-stent-in-small-vessels-and-long-lesions/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>St. Jude Medical Announces European Approval Of Next-Generation Athena Programmer For The Management Of Deep Brain Stimulation Therapy</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/24/st-jude-medical-announces-european-approval-of-next-generation-athena-programmer-for-the-management-of-deep-brain-stimulation-therapy/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/24/st-jude-medical-announces-european-approval-of-next-generation-athena-programmer-for-the-management-of-deep-brain-stimulation-therapy/#comments</comments>
		<pubDate>Fri, 24 Sep 2010 15:06:09 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Lab Software]]></category>
		<category><![CDATA[Athena(TM) programmer]]></category>
		<category><![CDATA[brain stimulation]]></category>
		<category><![CDATA[European CE Mark]]></category>
		<category><![CDATA[St. Jude Medical]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=353</guid>
		<description><![CDATA[St. Jude Medical, Inc. announced European CE Mark approval of its new Athena(TM) programmer, a deep brain stimulation (DBS) therapy management system. This next-generation platform offers clinicians a powerful yet easy-to-use interface that enables them to set or adjust therapeutic parameters to optimize patient results. Additionally, the system has the most comprehensive data management capacity [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-354" href="http://www.diagnosticsproductguide.com/blog/2010/09/24/st-jude-medical-announces-european-approval-of-next-generation-athena-programmer-for-the-management-of-deep-brain-stimulation-therapy/st-jude-medical/"><img class="alignright size-full wp-image-354" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/St.-Jude-Medical.png" border="0" alt="St. Jude Medical" width="200" height="35" /></a>St. Jude Medical, Inc. announced European CE Mark approval of its new Athena(TM) programmer, a deep brain stimulation (DBS) therapy management system. This next-generation platform offers clinicians a powerful yet easy-to-use interface that enables them to set or adjust therapeutic parameters to optimize patient results. Additionally, the system has the most comprehensive data management capacity on the market, which will aid clinicians in the organization and storage of patient information.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/201842.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/24/st-jude-medical-announces-european-approval-of-next-generation-athena-programmer-for-the-management-of-deep-brain-stimulation-therapy/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Siemens Leads By Example In IVD Industry Through Adopting GS1 Standards For Healthcare Product Identification</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/24/siemens-leads-by-example-in-ivd-industry-through-adopting-gs1-standards-for-healthcare-product-identification/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/24/siemens-leads-by-example-in-ivd-industry-through-adopting-gs1-standards-for-healthcare-product-identification/#comments</comments>
		<pubDate>Fri, 24 Sep 2010 15:02:58 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Equipment and Protective Gear]]></category>
		<category><![CDATA[Molecular Diagnostics]]></category>
		<category><![CDATA[GHX Health ConneXion™]]></category>
		<category><![CDATA[Global Data Synchronization Network]]></category>
		<category><![CDATA[GTIN]]></category>
		<category><![CDATA[Siemens Healthcare Diagnostics]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=359</guid>
		<description><![CDATA[Siemens Healthcare Diagnostics has published product data including GTINs for its complete U.S. product portfolio to the GHX Health ConneXion™ data pool, which is certified by GS1&#8242;s Global Data Synchronization Network (GDSN) to synchronize medical-surgical product data. The GS1 system of standards is the most widely used supply chain standards system in the world. Use [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-360" href="http://www.diagnosticsproductguide.com/blog/2010/09/24/siemens-leads-by-example-in-ivd-industry-through-adopting-gs1-standards-for-healthcare-product-identification/siemens-healthcare-diagnostics/"><img class="alignleft size-full wp-image-360" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/Siemens-Healthcare-Diagnostics.png" border="0" alt="Siemens Healthcare Diagnostics" width="200" height="40" /></a>Siemens Healthcare Diagnostics has published product data including GTINs for its complete U.S. product portfolio to the GHX Health ConneXion™ data pool, which is certified by GS1&#8242;s Global Data Synchronization Network (GDSN) to synchronize medical-surgical product data. The GS1 system of standards is the most widely used supply chain standards system in the world. Use of standards has proven highly effective in other industries, such as retail and consumer packaged goods.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/202081.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/24/siemens-leads-by-example-in-ivd-industry-through-adopting-gs1-standards-for-healthcare-product-identification/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Roche Receives FDA Clearance For U.S. Launch Of Cobas 8000 Modular Analyzer Series For High-Volume Laboratory Testing</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/14/roche-receives-fda-clearance-for-u-s-launch-of-cobas-8000-modular-analyzer-series-for-high-volume-laboratory-testing/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/14/roche-receives-fda-clearance-for-u-s-launch-of-cobas-8000-modular-analyzer-series-for-high-volume-laboratory-testing/#comments</comments>
		<pubDate>Tue, 14 Sep 2010 15:03:32 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[Laboratory Automation]]></category>
		<category><![CDATA[Microbiology and Virology]]></category>
		<category><![CDATA[Molecular Diagnostics]]></category>
		<category><![CDATA[510(k) clearance]]></category>
		<category><![CDATA[Clinical Chemistry]]></category>
		<category><![CDATA[cobas® 8000]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[immunochemistry]]></category>
		<category><![CDATA[modular analyzer series]]></category>
		<category><![CDATA[Roche Diagnostics]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=349</guid>
		<description><![CDATA[Roche Diagnostics announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the cobas® 8000 modular analyzer series, a Serum Work Area solution designed for diagnostic laboratories with a workload of 3-15 million clinical chemistry / immunochemistry tests per year. The cobas 8000 series is the newest member of the [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-350" href="http://www.diagnosticsproductguide.com/blog/2010/09/14/roche-receives-fda-clearance-for-u-s-launch-of-cobas-8000-modular-analyzer-series-for-high-volume-laboratory-testing/roche/"><img class="alignleft size-full wp-image-350" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/Roche.png" border="0" alt="Roche" width="200" height="89" /></a>Roche Diagnostics announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the cobas® 8000 modular analyzer series, a Serum Work Area solution designed for diagnostic laboratories with a workload of 3-15 million clinical chemistry / immunochemistry tests per year. The cobas 8000 series is the newest member of the Roche cobas modular platform family, which combines clinical chemistry and immunochemistry testing.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/200901.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/14/roche-receives-fda-clearance-for-u-s-launch-of-cobas-8000-modular-analyzer-series-for-high-volume-laboratory-testing/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Transgenomic Expands Distribution Of SURVEYOR(R) Scan K-RAS Mutation Detection Kit With CE IVD Mark</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/14/transgenomic-expands-distribution-of-surveyorr-scan-k-ras-mutation-detection-kit-with-ce-ivd-mark/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/14/transgenomic-expands-distribution-of-surveyorr-scan-k-ras-mutation-detection-kit-with-ce-ivd-mark/#comments</comments>
		<pubDate>Tue, 14 Sep 2010 14:56:00 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Genetic Testing]]></category>
		<category><![CDATA[CE IVD Mark]]></category>
		<category><![CDATA[European Union]]></category>
		<category><![CDATA[Mutation Detection]]></category>
		<category><![CDATA[SURVEYOR® Scan]]></category>
		<category><![CDATA[Transgenomic]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=345</guid>
		<description><![CDATA[Transgenomic, Inc. announced that it completed the requirements for CE IVD labeling and has expanded distribution of its SURVEYOR® Scan K-RAS mutation detection kit throughout most of the European Union. The SURVEYOR Scan K-RAS CE IVD kit is a member of Transgenomic&#8217;s family of mutation detection kits, which features proprietary SURVEYOR endonuclease technology. The SURVEYOR [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-346" href="http://www.diagnosticsproductguide.com/blog/2010/09/14/transgenomic-expands-distribution-of-surveyorr-scan-k-ras-mutation-detection-kit-with-ce-ivd-mark/transgenomic/"><img class="alignright size-full wp-image-346" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/Transgenomic.png" border="0" alt="Transgenomic" width="200" height="51" /></a>Transgenomic, Inc. announced that it completed the requirements for CE IVD labeling and has expanded distribution of its SURVEYOR® Scan K-RAS mutation detection kit throughout most of the European Union. The SURVEYOR Scan K-RAS CE IVD kit is a member of Transgenomic&#8217;s family of mutation detection kits, which features proprietary SURVEYOR endonuclease technology. The SURVEYOR Scan is a novel approach to mutation detection, which has been shown to provide comparable sensitivity than other commercial kits.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/200909.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/14/transgenomic-expands-distribution-of-surveyorr-scan-k-ras-mutation-detection-kit-with-ce-ivd-mark/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>The Optimal Set-Up For Obtaining The Best Breast Scan Image With Minimal Radiation Dose To The Patient</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/10/the-optimal-set-up-for-obtaining-the-best-breast-scan-image-with-minimal-radiation-dose-to-the-patient/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/10/the-optimal-set-up-for-obtaining-the-best-breast-scan-image-with-minimal-radiation-dose-to-the-patient/#comments</comments>
		<pubDate>Fri, 10 Sep 2010 05:29:37 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Cancer Testing]]></category>
		<category><![CDATA[breast cancers]]></category>
		<category><![CDATA[International Journal of Low Radiation]]></category>
		<category><![CDATA[mammography]]></category>
		<category><![CDATA[mathematical tool]]></category>
		<category><![CDATA[Monte Carlo]]></category>
		<category><![CDATA[University of Cordoba]]></category>
		<category><![CDATA[X-rays]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=341</guid>
		<description><![CDATA[A mathematical tool known as a Monte Carlo analysis could help improve the way X-rays are used for mammography and reduce the number of breast cancers missed by the technique and avoiding false positives, according to research published in the International Journal of Low Radiation. Researchers at the University of Cordoba have tested the different [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-342" href="http://www.diagnosticsproductguide.com/blog/2010/09/10/the-optimal-set-up-for-obtaining-the-best-breast-scan-image-with-minimal-radiation-dose-to-the-patient/breast-cancers/"><img class="alignleft size-full wp-image-342" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/breast-cancers.png" border="0" alt="breast cancers" width="200" height="170" /></a>A mathematical tool known as a Monte Carlo analysis could help improve the way X-rays are used for mammography and reduce the number of breast cancers missed by the technique and avoiding false positives, according to research published in the International Journal of Low Radiation. Researchers at the University of Cordoba have tested the different configurations used by radiographers to carry out X-ray mammography and analyzed the results statistically using the Monte Carlo technique.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/200216.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/10/the-optimal-set-up-for-obtaining-the-best-breast-scan-image-with-minimal-radiation-dose-to-the-patient/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>ForteBio Announces Launch Of Protein G Biosensor For Use On its Octet(R) Instruments</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/10/fortebio-announces-launch-of-protein-g-biosensor-for-use-on-its-octetr-instruments/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/10/fortebio-announces-launch-of-protein-g-biosensor-for-use-on-its-octetr-instruments/#comments</comments>
		<pubDate>Fri, 10 Sep 2010 05:20:48 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Equipment and Protective Gear]]></category>
		<category><![CDATA[Microbiology and Virology]]></category>
		<category><![CDATA[Molecular Diagnostics]]></category>
		<category><![CDATA[ammalian immunoglobulin (IgG)]]></category>
		<category><![CDATA[antibody molecule]]></category>
		<category><![CDATA[biosensor]]></category>
		<category><![CDATA[Dip and Read™ Protein]]></category>
		<category><![CDATA[ForteBio®]]></category>
		<category><![CDATA[International Standards Organization]]></category>
		<category><![CDATA[Octet instrumentation platform]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=336</guid>
		<description><![CDATA[ForteBio®, Inc. announced the launch of its Dip and Read™ Protein G biosensor for rapid detection and quantification of numerous types of mammalian immunoglobulin (IgG), an antibody molecule, from solution. Because it runs on the company&#8217;s label-free Octet instrumentation platform, the new biosensor enables such measurements with unprecedented speed, ease of use and cost-efficiency. The [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-337" href="http://www.diagnosticsproductguide.com/blog/2010/09/10/fortebio-announces-launch-of-protein-g-biosensor-for-use-on-its-octetr-instruments/fortebio/"><img class="alignright size-full wp-image-337" src="http://blog.diagnosticsproductguide.com/files/2010/09/ForteBio.png" border="0" alt="ForteBio" width="200" height="100" /></a>ForteBio®, Inc. announced the launch of its Dip and Read™ Protein G biosensor for rapid detection and quantification of numerous types of mammalian immunoglobulin (IgG), an antibody molecule, from solution. Because it runs on the company&#8217;s label-free Octet instrumentation platform, the new biosensor enables such measurements with unprecedented speed, ease of use and cost-efficiency. The company also announced that it has completed International Standards Organization (ISO) certification of its biosensor manufacturing facility.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/200027.php" target="_blank">here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://blog.diagnosticsproductguide.com/2010/09/10/fortebio-announces-launch-of-protein-g-biosensor-for-use-on-its-octetr-instruments/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<item>
		<title>Endologix Receives CE Mark Approval For Expanded Line Of Powerlink Products And PowerFit Aortic Extensions</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/01/endologix-receives-ce-mark-approval-for-expanded-line-of-powerlink-products-and-powerfit-aortic-extensions/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/01/endologix-receives-ce-mark-approval-for-expanded-line-of-powerlink-products-and-powerfit-aortic-extensions/#comments</comments>
		<pubDate>Wed, 01 Sep 2010 09:00:41 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Cardiology]]></category>
		<category><![CDATA[FDA Approval]]></category>
		<category><![CDATA[CE Mark]]></category>
		<category><![CDATA[Endologix]]></category>
		<category><![CDATA[European Union]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[PowerFit™ Aortic Extensions]]></category>
		<category><![CDATA[Powerlink®]]></category>
		<category><![CDATA[stent graft]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=332</guid>
		<description><![CDATA[Endologix, Inc. announced that it received CE Mark approval to market its expanded offering of Powerlink® stent graft products and PowerFit™ Aortic Extensions in the European Union. The Company expects to launch the products in a limited market release in Europe during the fourth quarter of 2010, followed by a full product launch in 2011. [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-333" href="http://www.diagnosticsproductguide.com/blog/2010/09/01/endologix-receives-ce-mark-approval-for-expanded-line-of-powerlink-products-and-powerfit-aortic-extensions/endologix/"><img class="alignleft size-full wp-image-333" style="margin: 5px" src="http://blog.diagnosticsproductguide.com/files/2010/09/Endologix.png" border="0" alt="Endologix" width="200" height="94" /></a>Endologix, Inc. announced that it received CE Mark approval to market its expanded offering of Powerlink® stent graft products and PowerFit™ Aortic Extensions in the European Union. The Company expects to launch the products in a limited market release in Europe during the fourth quarter of 2010, followed by a full product launch in 2011. Endologix recently received U.S. Food and Drug Administration (FDA) approval for these new products and they are currently in a limited market release in the U.S., with a full market release in the U.S. planned for the fourth quarter of 2010.</p>
<p>Read the fulls story <a href="http://www.medicalnewstoday.com/articles/199278.php" target="_blank">here</a></p>
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		<title>Toolbox Of MiniPromoters For Gene Research And Therapy Unvelied By UBC Researchers</title>
		<link>http://blog.diagnosticsproductguide.com/2010/09/01/toolbox-of-minipromoters-for-gene-research-and-therapy-unvelied-by-ubc-researchers/</link>
		<comments>http://blog.diagnosticsproductguide.com/2010/09/01/toolbox-of-minipromoters-for-gene-research-and-therapy-unvelied-by-ubc-researchers/#comments</comments>
		<pubDate>Wed, 01 Sep 2010 08:46:51 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Cancer Testing]]></category>
		<category><![CDATA[Genetic Testing]]></category>
		<category><![CDATA[brain]]></category>
		<category><![CDATA[eye function]]></category>
		<category><![CDATA[genes]]></category>
		<category><![CDATA[human DNA]]></category>
		<category><![CDATA[MiniPromoters]]></category>
		<category><![CDATA[spinal cord]]></category>
		<category><![CDATA[therapeutic genetic medicine]]></category>
		<category><![CDATA[University of British Columbia]]></category>
		<guid isPermaLink="false">http://www.diagnosticsproductguide.com/blog/?p=327</guid>
		<description><![CDATA[University of British Columbia researchers have led the development of a new &#8220;toolbox of MiniPromoters&#8221; for research and future therapies on brain, spinal cord and eye function. MiniPromoters are small segments of human DNA with the ability to turn genes on and off at specific times and locations. They&#8217;re important tools used by scientists and [...]]]></description>
			<content:encoded><![CDATA[<p><a rel="attachment wp-att-328" href="http://www.diagnosticsproductguide.com/blog/2010/09/01/toolbox-of-minipromoters-for-gene-research-and-therapy-unvelied-by-ubc-researchers/university-of-british-columbia/"><img class="alignright size-full wp-image-328" src="http://blog.diagnosticsproductguide.com/files/2010/09/University-of-British-Columbia.png" border="0" alt="University of British Columbia" width="200" height="203" /></a>University of British Columbia researchers have led the development of a new &#8220;toolbox of MiniPromoters&#8221; for research and future therapies on brain, spinal cord and eye function. MiniPromoters are small segments of human DNA with the ability to turn genes on and off at specific times and locations. They&#8217;re important tools used by scientists and clinicians to mark cells, explore function and deliver therapeutic genetic medicine.</p>
<p>Read the full story <a href="http://www.medicalnewstoday.com/articles/199468.php" target="_blank">here</a></p>
]]></content:encoded>
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