scispace - formally typeset
Search or ask a question
Author

Lars Tenerz

Bio: Lars Tenerz is an academic researcher from Uppsala University. The author has contributed to research in topics: Pressure sensor & Wafer. The author has an hindex of 19, co-authored 41 publications receiving 2054 citations.

Papers
More filters
Patent
24 Apr 2003
TL;DR: A dissolvable medical sealing device (3, 4, 6, 7, 9) for closing a wound in vessel is described in this paper. But it is not shown how to construct such a sealing device.
Abstract: The present invention provides a dissolvable medical sealing device (3, 4; 6, 7; 9) for closing a wound in vessel. A sealing device (3, 4; 6, 7; 9) according to the invention is made of a material that dissolves by means of physical processes, rather than by means of chemical or biological processes. Such a sealing device (3, 4; 6, 7; 9) can be made of polyethylene glycol, polypropylene glycol, copolymers containing ethylene glycol and propylene glycol, polyvinyl alcohol or polyvinyl pyrolidone, or any combinations thereof.

670 citations

Journal ArticleDOI
TL;DR: Fracture testing of silicon cantilever beams (thicknesses 10-20 μm) was performed in situ in a scanning electron microscope by means of an equipment specially designed for this purpose as mentioned in this paper.
Abstract: Fracture testing of silicon cantilever beams (thicknesses 10–20 μm) was performed in situ in a scanning electron microscope by means of an equipment specially designed for this purpose. Beams of various sizes and orientations (〈011〉 and 〈001〉) were manufactured in Si (100) wafers by two different micromachining procedures. The beams were tested by simple bending to fracture, and a number of fundamental fracture parameters were determined from an analytical model of elastic fracture. To verify its validity, the model was utilized to evaluate an experimental E modulus, which was found to agree well with previous results. Fracture limits, fracture strains, and initiating flaw sizes were determined. The maximum fracture limit was very high; about 10 GPa. The strengths of different beams scattered from this value down to practically zero strength, with an average close to 4 GPa. The corresponding fracture strains and initiating flaw sizes were 6% and 3 nm, respectively (maximum strength), and 2% and 17 nm (ave...

216 citations

Patent
23 Feb 2006
TL;DR: A sensor and guide wire assembly includes a core wire having a distal end, a proximal end, and a plurality of sections of different cross sections and thereby different flexibilities.
Abstract: A sensor and guide wire assembly includes a core wire having a distal end, a proximal end, and a plurality of sections of different cross sections and thereby different flexibilities. At least one of the core wire sections has an enlarged portion with a sensor receptacle therein. The assembly also includes a tube that encloses the core wire over at least a fraction of its length such that the core wire extends out from a distal end of the tube. The tube is configured to enable the sensor and guide wire assembly to be inserted into an artery and to be passed to a measurement site inside a patient's body. The assembly further includes a sensor mounted in the sensor receptacle of the enlarged portion of the core wire. A first coil is arranged to enclose a first portion of the core wire extending out from the distal end of the tube, and the first coil is located nearer to the proximal end of the core wire than the sensor. A second coil is arranged to enclose a second portion of the core wire extending out from the distal end of the tube. The second coil is located nearer to the distal end of the core wire than the sensor.

185 citations

Patent
18 Jun 1996
TL;DR: In this paper, a sensor/guide wire device for biological pressure measurements has been proposed, which is mounted in a cantilevering fashion such that a pressure sensitive end of the sensor does not contact any structure other than its mount.
Abstract: The invention relates to a sensor/guide wire device for biological pressure measurements having a guide wire (16, 17, 18, 21, 23) having a distal and a proximal end, and a pressure sensor device (19) mounted at the distal end of the guide wire. The distal portion can be a solid wire member (16) surrounded by a spiral member (18), and the sensor (19) can be an electrical sensor of a piezoresistive type. The sensor (19) is mounted on the solid wire (16). The sensor is mounted in a cantilevering fashion such that a pressure sensitive end of the sensor does not contact any structure other than its mount. This prevents forces (bending artifacts) from being exerted on the sensor, which could otherwise interfere with pressure measurements.

123 citations

Patent
25 Mar 1998
TL;DR: In this article, the authors present a guide wire assembly, comprising of a proximal end and a distal end, where a measuring device is mounted in the proximal portion of the guide wire.
Abstract: The invention relates to a guide wire assembly, comprising a guide wire (2) having a distal end portion (16) and a proximal end, wherein a measuring device (14) is mounted in the distal end portion (16) of said guide wire (2). It also has an interface cable (4) having a first end connectable to a control unit (8), and a second end connectable to the proximal end of said guide wire. Furthermore there is provided information storing means (20; 22; Rx) on said interface cable, containing calibration-/temperature compensation data, uniquely characteristic of said measuring device. The data and an uncompensated output from said measuring device forming the input for calculation of a correct measurement value.

117 citations


Cited by
More filters
Patent
10 Jun 2011
TL;DR: In this article, a surgical stapling device particularly suited for endoscopic procedures is described, which includes a handle assembly and an elongated body extending distally from the handle assembly.
Abstract: A surgical stapling device particularly suited for endoscopic procedures is described The device includes a handle assembly and an elongated body extending distally from the handle assembly The distal end of the elongated body is adapted to engage a disposable loading unit A control rod having a proximal end operatively connected to the handle assembly includes a distal end extending through the elongated body A control rod locking member is provided to prevent movement of the control rod until the disposable loading unit is fully secured to the elongated body of the stapling device

2,013 citations

Patent
30 Sep 2004
TL;DR: In this paper, a surgical stapling instrument (1) comprises a body portion (2, 3), a handle (4), and a staple fastening assembly (8), which includes a curved cartridge (10), which comprises at least one curved open row of staples, and a curved anvil (22), which is adapted to cooperate with the cartridge for forming the ends of the staples exiting from the cartridge.
Abstract: A surgical stapling instrument (1) comprises a body portion (2, 3), a handle (4) and a staple fastening assembly (8). The staple fastening assembly (8) includes a curved cartridge (10), which comprises at least one curved open row of staples, and a curved anvil (22), which is adapted to cooperate with the cartridge (10) for forming the ends of the staples exiting from the cartridge (10). The staple fastening assembly (8) is adapted to allow unobstructed access towards the concave inner faces of the cartridge (10) and the anvil (22). The cartridge (10) can be moved towards the anvil (22) from a spaced position for positioning tissue therebetween to a closed position for clamping the tissue. Preferably, a knife is contained within the cartridge (10) and is positioned such that there is at least one row of staples on at least one side of the knife.

1,502 citations

Patent
14 Jun 2016
TL;DR: Newness and distinctiveness is claimed in the features of ornamentation as shown inside the broken line circle in the accompanying representation as discussed by the authors, which is the basis for the representation presented in this paper.
Abstract: Newness and distinctiveness is claimed in the features of ornamentation as shown inside the broken line circle in the accompanying representation.

1,500 citations

Patent
21 Apr 2011
TL;DR: In this paper, a surgical instrument can comprise a channel configured to support a staple cartridge and, in addition, an anvil pivotable between open and closed positions relative to the channel.
Abstract: A surgical instrument can comprise a channel configured to support a staple cartridge and, in addition, an anvil pivotable between open and closed positions relative to the channel. The surgical instrument can further comprise a cutting member configured to incise tissue positioned captured between the staple cartridge and the anvil and, in addition, means for stopping the cutting member prior to a distal end datum, wherein the distal end datum can be defined by the distal-most staple cavity in the staple cartridge. In such embodiments, the incision within the tissue may not extend beyond the portion of the tissue that has been stapled.

1,498 citations

Patent
19 Jun 1996
TL;DR: In this article, the authors present a controller that can cause the generator to supply a blended output signal alternating constantly between a first output signal across the output connections in which the radio frequency output voltage developed across output connections is limited to at least a first predetermined threshold value for cutting or vaporization of tissue, and a second output signal with a power supply coupled to the output stage for supplying power to output stage.
Abstract: In an electrosurgical generator for generating radio frequency power, the generator includes a radio frequency output stage having two or more output connections, and a power supply coupled to the output stage for supplying power to the output stage. A controller is operable to cause the generator to supply a blended output signal alternating constantly between a first output signal across the output connections in which the radio frequency output voltage developed across the output connections is limited to at least a first predetermined threshold value for cutting or vaporisation of tissue, and a second output signal across the output connections in which the radio frequency output voltage developed across the output connections is limited to a second threshold value for coagulation. There is also provided adjustment means, operable by a user of the electrosurgical generator, for changing between various preset settings for the blended signal, the preset settings each having a predetermined duty cycle of the blended signal that is limited to the first threshold value for cutting or vaporisation, and a predetermined duty cycle of the blended signal that is limited to the second threshold value for coagulation.

1,486 citations