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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Jan. 31, 2012

View Archived Issues

Report from Europe: Custom Spine receives CE mark for its current U.S. products

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Washington roundup: Whistleblowers sue FDA over surveillance of personal e-mail

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Agreements/contracts: Cardinal, Cook distribute vascular access products

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New ventures: Aperture subsidiary in JV with Reliable Medical

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Deals roundup: Bain Capital completes $487M Physio-Control acquisition

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Med-Tech Notes

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Court report: Ortho Caps opposes Align's dental fabrication models

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Product Briefs

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People in the News

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MDD's Cardio Extra

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Medtronic receives FDA nod for DF4 High-Voltage Connector

Medtronic (Minneapolis) reported FDA approval and launch of the DF4 High-Voltage Connector System, a right ventricular lead and connector used with implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) to detect and accurately treat potentially life-threatening heart rhythms. The DF4 Connector System helps simplify implantation procedures via a redesigned port and provides additional reliability by giving physicians visual confirmation of the lead connection to the device. (Medical Device Daily) Read More

Financings roundup: ConforMIS raises $89 million in its Series E funding round

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