Pulse Technologies, Inc. Dec 2010 - Apr 2013
Technical Sales Specialist
Ocular Therapeutix, Inc Feb 2008 - Dec 2010
Engineering Manager, New Product Development
Boston Scientific Aug 2006 - Feb 2008
Product Development Engineer
Medtronic 2002 - 2006
Product Development Engineer
Education:
Babson College - Franklin W. Olin Graduate School of Business 2007 - 2010
MBA, Business
University of Massachusetts at Lowell 1999 - 2003
Bachelor of Science, Plastics Engineering
Skills:
Medical Devices Product Development R&D Fda Cross Functional Team Leadership Market Development Product Launch Iso 13485 Commercialization Manufacturing Design Control Sales Engineering Management Business Development Capital Equipment Product Design Start Ups Biomedical Engineering Research and Development U.s. Food and Drug Administration Marketing Strategy Program Management V&V Continuous Improvement Iso Lean Manufacturing Quality System Injection Molding Design of Experiments Biotechnology Orthopedic Validation Project Management
A medical guidewire having a core-to-tip construction that includes a core wire region surrounded by a flexible coil. The core wire having a distal tip segment that includes a proximal flat drop axially separated from a distal flat drop by a cylindrical or frusto-conical linking portion. The proximal and distal flat drops each having a pair of parallel planar surfaces, wherein the planar surfaces of the proximal flat drop are at an angle to the planar surfaces of the distal flat drop. The tip construction provides improved flexibility while maintaining columnar strength and providing excellent torsional characteristics.
James F. Biggins - Waltham MA, US Todd A. Peavey - Denver CO, US
Assignee:
SENTIAL, LLC - Salem MA
International Classification:
G08B 21/00 A43B 23/26 A43B 13/00
US Classification:
34087016, 36 54, 36 25 R
Abstract:
A wear monitor for footgear can indicate when a shoe or component may have exceeded its expected useful life. The indication can be triggered by a measure of use, such as steps taken or distance accrued in the shoes, either through estimation or actual measurements. The monitor can take into account varies parameters related to the individual wearer of the shoe and environmental factors to more accurately determine when a pair of shoes has reached a wear out period. By employing sensors, the monitor can also be measure certain operating parameters of the shoe, such as the loss of a critical amount of resilience, and indicating to the wearer that the shoes are no longer adequate to protect the wearer from injury. The wear monitor can be fabricated into the shoe during manufacturing or can be a portable stand-alone device and can employ various technologies to provide a status indication to the wearer.
Endoprosthesis With Filament Repositioning Or Retrieval Member And Guard Structure
Srinath Tupil - Acton MA, US James Biggins - Waltham MA, US William Bertolino - Framingham MA, US
Assignee:
BOSTON SCIENTIFIC SCIMED, INC. - Maple Grove MN
International Classification:
A61F 2/82
US Classification:
623 115
Abstract:
An endoprosthesis includes a stent structure having an elongate member longitudinal portions of which overlap to define the crossover structures. The stent structure may also include loop structures, which are contiguous with the crossover structures, through which a filament extends. A guard structure is secured to the stent structure and located adjacent to the crossover structures to obstruct displacement of the filament between the longitudinal portions of the elongate member of the crossover structures. A method for operating the endoprosthesis includes displacing the loop structures toward one another along the filament to displaced positions relative to the suture structure for reducing the respective profiles of the stent structure and patch structure.
Flowable Hydrogels For Control Of Cell In-Migration
A guiding catheter for placement in a patient's vessel. The catheter includes an elongate hollow shaft with open proximal and distal ends and a bore extending there through. The catheter shaft includes an inner liner, a metallic reinforcement layer overlying the inner liner, and a unitary outer jacket covering the reinforcement layer. A distal portion of the outer jacket of the catheter shaft is chemically softened to be more flexible than a proximal portion of the outer jacket. A connector fitting is mounted at the proximal end of the shaft in communication with the bore and a distal tip is attached to the distal end of the shaft. A method of manufacturing the guiding catheter is also disclosed.
High Strength Porous Materials For Controlled Release
High strength biomedical materials and processes for making the same are disclosed. Included in the disclosure are nanoporous hydrophilic solids that can be extruded with a high aspect ratio to make high strength medical catheters and other devices with lubricious and biocompatible surfaces. Biologically active agents may be entrapped in pores of materials to provide a controlled release of the biologically active agent.
High Strength Porous Materials Incorporating Water Soluble Polymers
High strength biomedical materials and processes for making the same are disclosed. Included in the disclosure are nanoporous hydrophilic solids that can be extruded with a high aspect ratio to make high strength medical catheters and other devices with lubricious and biocompatible surfaces. Polymers may be entrapped in pores of materials to provide a durable modification of the materials.
Endoprosthesis With Filament Repositioning Of Retrieval Member And Guard Structure
- Maple Grove MN, US James Biggins - Waltham MA, US William Bertolino - Framingham MA, US
Assignee:
BOSTON SCIENTIFIC SCIMED INC. - Maple Grove MN
International Classification:
A61F 2/88 A61F 2/90
US Classification:
623 133
Abstract:
An endoprosthesis includes a stent structure having an elongate member longitudinal portions of which overlap to define the crossover structures. The stent structure may also include loop structures, which are contiguous with the crossover structures, through which a filament extends. A guard structure is secured to the stent structure and located adjacent to the crossover structures to obstruct displacement of the filament between the longitudinal portions of the elongate member of the crossover structures. A method for operating the endoprosthesis includes displacing the loop structures toward one another along the filament to displaced positions relative to the suture structure for reducing the respective profiles of the stent structure and patch structure.
Amazon
Historians of York (St. Anthony's Hall publications)
know what's going on. This is a movie that is truly made by the fans, for the fans. That is not to say this is a perfect movie. But I have to applaud the visionary story telling by this team who refused the formulaic tropes of modern mainstream film making. RATING 9 (of 10) (James Biggins)