Robert T. V. Kung - Auburn MA David M. Lederman - Marblehead MA Meir Rosenberg - Newton MA
Assignee:
Abiomed, Inc. - Danvers MA
International Classification:
A61F 202
US Classification:
600 37
Abstract:
Artificial implantable active and passive girdles include a heart assist system with an artificial myocardium employing a number of flexible, non-distensible tubes with the walls along their long axes connected in series to form a cuff and a passive girdle is wrapped around a heart muscle which has dilatation of a ventricle to conform to the size and shape of the heart and to constrain the dilatation during diastole. The passive girdle is formed of a material and structure that does not expand away from the heart but may, over an extended period of time be decreased in size as dilatation decreases.
Terri K. Taylor - Marlborough MA Meir Rosenberg - Newton MA Rainuka Gupta - Cambridge MA Stephen F. Wilson - Raynham MA Pierre S. Ostiguy - Rochester MA Bertil Romner - Lund, SE Alan J. Dextradeur - Franklin MA
Assignee:
Codman Shurtleff, Inc. - Raynham MA
International Classification:
A61B 800
US Classification:
600437
Abstract:
An acoustic monitoring system that is able to verify the success or failure of the positional adjustment of a valve without the need for additional energy during non-invasive reprogramming is provided. The acoustic monitoring system includes a programmer for generating a sequence of commands to adjust the valve mechanism, and for receiving acoustic signals for analysis, a transmitter to implement the command and adjust the valve, and a sensor for detecting an acoustic signal generated from the valve during execution of the commands. A method for using the acoustic monitoring system is also provided.
An anti-siphon shunt device is provided that is insensitive to body postural changes. The shunt device has a housing having a chamber, an inlet port, and an outlet port. A valve mechanism disposed within the housing manages fluid movement into and out of the chamber over a pressure gradient. The valve mechanism includes a blocking element configured to seat against an opening in a barrier mounted within the chamber for preventing fluid flow therethrough. A pressure sensor having a conformable membrane detects the external pressure surrounding the chamber and communicates with a biasing element to exert a biasing force against a first surface of the blocking element, while a second surface of the blocking element is acted upon by a countervailing pressure in a direction opposite the biasing force. The conformable membrane can be enclosed within a housing to protect the device from shutting off when a patient inadvertently lies on the valve mechanism.
Meir Rosenberg - Newton MA, US Pierre Ostiguy - Hampshire MA, US
Assignee:
Codman & Shurtleff, Inc. - Raynham MA
International Classification:
A61M 5/00
US Classification:
604 8, 604 7, 604264
Abstract:
An implantable fluid management device includes a catheter with an elongate proximal portion, a flexible distal portion, and a fluid passageway flowing therethrough. The distal portion includes a coil-shaped portion that defines a spiral having at least one turn. The distal portion of the catheter includes at least one pore in fluid communication with the fluid passageway of the catheter, which is located on an internal portion of the spiral. The positioning of the pore(s) on the internal portion of the spiral protects the pore(s) from obstruction or occlusion caused by tissue growing into or around the catheter.
A self adjusting hydrocephalus valve that continuously drains cerebrospinal fluid at a rate which is proportional to the average pressure difference across the valve. The valve employs a ball-in-cone mechanism having an associated biasing element that is insensitive to high frequency pressure variations for regulating the opening of the valve mechanism. The biasing element includes flexible bellows having a preset tension.
Meir Rosenberg - Newton MA, US Douglas MacBride - Walpole MA, US
Assignee:
Codman & Shurtleff, Inc. - Raynham MA
International Classification:
A61K 9/22
US Classification:
6048911
Abstract:
A valve that is adapted to control the flow rate of fluid flow from an implantable pump or other fluid delivery device is provided. In general, the valve includes a multi-lumen member that is adapted to receive fluid-flow therethrough, and a restrictor member that is coupled to the multi-lumen member such that the restrictor member is effective to selectively restrict at least a portion of one or more lumens in the multi-lumen member to thereby adjust the flow rate of fluid flowing through the multi-lumen member. The valve can be built into an implantable drug pump to control fluid flow exiting the pump, or alternatively the valve can disposed within a catheter or otherwise coupled to an outlet port in an implantable drug pump to control the flow rate of fluid exiting the drug pump.
Terri K. Taylor - Marlborough MA, US Meir Rosenberg - Newton MA, US Rainuka Gupta - Cambridge MA, US Stephen Ferrer Wilson - Raynham MA, US Pierre S. Ostiguy - Rochester MA, US Bertil Romner - Lund, SE Alan J. Dextradeur - Franklin MA, US
An acoustic monitoring system that is able to verify the success or failure of the positional adjustment of a valve without the need for additional energy during non-invasive reprogramming is provided. The acoustic monitoring system includes a programmer for generating a sequence of commands to adjust the valve mechanism, and for receiving acoustic signals for analysis, a transmitter to implement the command and adjust the valve, and a sensor for detecting an acoustic signal generated from the valve during execution of the commands. A method for using the acoustic monitoring system is also provided.
Meir Rosenberg - Newton MA, US Douglas MacBride - Walpole MA, US
Assignee:
Codman & Shurtleff, Inc. - Raynham MA
International Classification:
A61M 5/00
US Classification:
604246
Abstract:
A valve that is adapted to control the flow rate of fluid flow from an implantable pump or other fluid delivery device is provided. In general, the valve includes a multi-lumen member that is adapted to receive fluid-flow therethrough, and a restrictor member that is coupled to the multi-lumen member such that the restrictor member is effective to selectively restrict at least a portion of one or more lumens in the multi-lumen member to thereby adjust the flow rate of fluid flowing through the multi-lumen member. The valve can be built into an implantable drug pump to control fluid flow exiting the pump, or alternatively the valve can disposed within a catheter or otherwise coupled to an outlet port in an implantable drug pump to control the flow rate of fluid exiting the drug pump.
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