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公开(公告)号：USD721815S1
公开(公告)日：2015-01-27
申请号：US29452860
申请日：2013-04-22
Applicant: Medtronic, Inc
Designer： David Lura , Martin Gerber , Bryant Pudil , Thomas Meyer , Brian Mullins
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公开(公告)号：USD713042S1
公开(公告)日：2014-09-09
申请号：US29446285
申请日：2013-02-21
Applicant: Medtronic, Inc.
Designer： Martin Gerber , David Lura , Bryant Pudil , Thomas Meyer , Brian Mullins
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公开(公告)号：USD711543S1
公开(公告)日：2014-08-19
申请号：US29446283
申请日：2013-02-21
Applicant: Medtronic, Inc.
Designer： Martin Gerber , David Lura , Bryant Pudil , Thomas Meyer , Brian Mullins
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公开(公告)号：US11759557B2
公开(公告)日：2023-09-19
申请号：US17034250
申请日：2020-09-28
Applicant: Medtronic, Inc.
Inventor： Martin Gerber , John Burnes , SuPing Lyu , Venkatesh R. Manda , Bryant Pudil
IPC: A61M1/16 , A61B5/00 , A61M1/00 , A61B5/053 , G16H20/17 , G16H40/63 , A61B5/145 , A61M1/34 , A61M1/36 , A61M1/14 , B01D61/00 , B01D61/32 , A61B5/0295 , A61B5/0537 , B01D65/02 , G16Z99/00 , G16H20/40 , A61B5/026 , A61M1/28
CPC classification number: A61M1/1603 , A61B5/0031 , A61B5/026 , A61B5/0295 , A61B5/053 , A61B5/0537 , A61B5/145 , A61B5/14503 , A61B5/14535 , A61B5/14539 , A61B5/14546 , A61B5/4836 , A61B5/4848 , A61B5/6866 , A61M1/00 , A61M1/14 , A61M1/16 , A61M1/1601 , A61M1/1605 , A61M1/1607 , A61M1/1613 , A61M1/28 , A61M1/34 , A61M1/342 , A61M1/3403 , A61M1/361 , A61M1/3607 , A61M1/3609 , A61M1/3612 , B01D61/00 , B01D61/32 , B01D65/02 , G16H20/17 , G16H20/40 , G16H40/63 , G16Z99/00 , A61B2560/0223 , A61M2205/04 , A61M2205/18 , A61M2205/33 , A61M2205/3303 , A61M2205/3306 , A61M2205/3313 , A61M2205/3331 , A61M2205/3334 , A61M2205/3375 , A61M2205/3523 , A61M2205/50 , A61M2205/52 , A61M2205/60 , A61M2205/70 , A61M2230/00 , A61M2230/005 , A61M2230/20 , A61M2230/207 , A61M2230/208 , A61M2230/65 , B01D2321/12 , B01D2321/40
Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.
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公开(公告)号：US10967112B2
公开(公告)日：2021-04-06
申请号：US15693535
申请日：2017-09-01
Applicant: Medtronic, Inc.
Inventor： Martin Gerber , John Burnes , SuPing Lyu , VenKatesh R. Manda , Bryant Pudil
IPC: A61M1/16 , A61B5/145 , A61B5/00 , A61M1/34 , A61M1/36 , A61M1/00 , A61M1/14 , A61B5/0295 , A61B5/053 , A61B5/026 , A61M1/28 , B01D61/00 , B01D61/32 , B01D65/02 , A61B5/0537 , G06F19/00
Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.
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Patent Agency Ranking
公开(公告)号：US20210008265A1
公开(公告)日：2021-01-14
申请号：US17034250
申请日：2020-09-28
Applicant: Medtronic, Inc.
Inventor： Martin Gerber , John Burnes , SuPing Lyu , VenKatesh R. Manda , Bryant Pudil
IPC: A61M1/16 , A61B5/145 , A61B5/00 , A61M1/34 , A61M1/36 , A61M1/00 , A61M1/14 , B01D61/00 , B01D61/32 , A61B5/0295 , A61B5/053 , B01D65/02 , A61B5/026 , A61M1/28
Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.
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公开(公告)号：US10406268B2
公开(公告)日：2019-09-10
申请号：US15067559
申请日：2016-03-11
Applicant: Medtronic, Inc.
Inventor： Martin Gerber , Suping Lyu , Bryant Pudil
IPC: A61M1/16 , A61M1/36 , B01D61/32 , B01D65/02 , A61M1/14 , A61M1/34 , A61B5/145 , A61B5/00 , A61B5/026 , A61B5/053 , A61M1/00 , A61B5/0295 , B01D61/00 , A61M1/28 , G06F19/00
Abstract: Monitoring of the performance of a blood fluid removal medium of a blood fluid removal device includes monitoring of condition, such as fluid flow rate or concentration of blood waste product, downstream of the medium. Upstream monitoring of the condition may also be performed to enhance the ability to determine whether the blood fluid removal medium is performing within predetermined ranges.
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公开(公告)号：US10064985B2
公开(公告)日：2018-09-04
申请号：US15384912
申请日：2016-12-20
Applicant: MEDTRONIC, INC.
Inventor： Martin Gerber , Suping Lyu , Bryant Pudil
IPC: A61B5/00 , A61M1/16 , A61B5/145 , A61B5/026 , A61B5/053 , A61M1/34 , B01D65/02 , A61M1/00 , A61B5/0295 , A61M1/14 , B01D61/00 , B01D61/32 , A61M1/36 , A61M1/28 , B01D11/00
Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patent parameters. By comparing the patient's current parameters to past parameters in response to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.
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公开(公告)号：US09968721B2
公开(公告)日：2018-05-15
申请号：US14554338
申请日：2014-11-26
Applicant: Medtronic, Inc.
Inventor： Martin Gerber , John Burnes , Suping Lyu , VenKatesh R. Manda , Bryant Pudil
IPC: A61M37/00 , A61M1/16 , A61B5/145 , A61B5/00 , A61B5/026 , A61B5/053 , A61M1/34 , B01D65/02 , A61M1/00 , A61B5/0295 , A61M1/14 , B01D61/00 , B01D61/32 , A61M1/36 , A61M1/28
CPC classification number: A61M1/1603 , A61B5/0031 , A61B5/026 , A61B5/0295 , A61B5/053 , A61B5/0537 , A61B5/145 , A61B5/14503 , A61B5/14535 , A61B5/14539 , A61B5/14546 , A61B5/4836 , A61B5/4848 , A61B5/4875 , A61B5/6866 , A61B5/7282 , A61B2560/0223 , A61M1/00 , A61M1/14 , A61M1/16 , A61M1/1601 , A61M1/1605 , A61M1/1607 , A61M1/1613 , A61M1/28 , A61M1/34 , A61M1/3403 , A61M1/342 , A61M1/3607 , A61M1/3609 , A61M1/361 , A61M1/3612 , A61M1/3672 , A61M2202/0498 , A61M2205/04 , A61M2205/18 , A61M2205/33 , A61M2205/3303 , A61M2205/3306 , A61M2205/3313 , A61M2205/3331 , A61M2205/3334 , A61M2205/3375 , A61M2205/3523 , A61M2205/50 , A61M2205/502 , A61M2205/52 , A61M2205/60 , A61M2205/70 , A61M2230/00 , A61M2230/005 , A61M2230/06 , A61M2230/20 , A61M2230/207 , A61M2230/208 , A61M2230/65 , B01D61/00 , B01D61/32 , B01D65/02 , B01D2321/12 , B01D2321/40 , G06F19/00
Abstract: A method includes monitoring an indicator of fluid volume of a patient via a sensor device, and setting an initial fluid volume removal prescription for a blood fluid removal session based on the monitored indicator of fluid volume. The method may further include transmitting data regarding the indicator of fluid volume from the implantable sensor device to fluid removal device. The system includes a blood fluid removal device and control electronics configured to set the initial fluid removal volume and rate prescription. In some embodiments, the fluid removal device sets or calculated the initial fluid volume removal prescription based on the data received from the implantable sensor. The indicator of fluid volume may be an indicator of tissue fluid volume or an indicator of blood fluid volume.
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公开(公告)号：US20170100529A1
公开(公告)日：2017-04-13
申请号：US15384912
申请日：2016-12-20
Applicant: MEDTRONIC, INC.
Inventor： Martin Gerber , Suping Lyu , Bryant Pudil
CPC classification number: A61M1/1603 , A61B5/0031 , A61B5/026 , A61B5/0295 , A61B5/053 , A61B5/0537 , A61B5/145 , A61B5/14503 , A61B5/14535 , A61B5/14539 , A61B5/14546 , A61B5/4836 , A61B5/4848 , A61B5/4875 , A61B5/6866 , A61B5/7282 , A61B2560/0223 , A61M1/00 , A61M1/14 , A61M1/16 , A61M1/1601 , A61M1/1605 , A61M1/1607 , A61M1/1613 , A61M1/28 , A61M1/34 , A61M1/3403 , A61M1/342 , A61M1/3607 , A61M1/3609 , A61M1/361 , A61M1/3612 , A61M1/3672 , A61M2202/0498 , A61M2205/04 , A61M2205/18 , A61M2205/33 , A61M2205/3303 , A61M2205/3306 , A61M2205/3313 , A61M2205/3331 , A61M2205/3334 , A61M2205/3375 , A61M2205/3523 , A61M2205/50 , A61M2205/502 , A61M2205/52 , A61M2205/60 , A61M2205/70 , A61M2230/00 , A61M2230/005 , A61M2230/06 , A61M2230/20 , A61M2230/207 , A61M2230/208 , A61M2230/65 , B01D61/00 , B01D61/32 , B01D65/02 , B01D2321/12 , B01D2321/40 , G06F19/00
Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patent parameters. By comparing the patient's current parameters to past parameters in response to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.
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