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公开(公告)号:US10575715B2
公开(公告)日:2020-03-03
申请号:US15563807
申请日:2016-03-31
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Rudolf Maria Jozef Voncken , Jacob Roger Haartsen , Maurice Hubertus Elisabeth Van Der Beek
Abstract: A deflectable medical device (1) includes a shape memory alloy wire (15) integrated into a flexible elongated body (11). The shape memory alloy wire (15) is arranged to shorten upon receiving energy from an energy supply (2,4), thereby deflecting the medical device (1). A rod (18) positioned in a lumen (14) of the flexible elongated body (11) and compressed between a fixture (16) in the proximal end (12) of the elongated body (11) and the distal end (13) of the elongated body (11) is responsible for the shape memory alloy wire (15) recovering its initial length upon discontinuation of energy supply.
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公开(公告)号:US11376385B2
公开(公告)日:2022-07-05
申请号:US15105675
申请日:2014-12-15
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Mareike Klee , Nocolaas Petrus Willard , Joyce Van Zanten , Lutz Christian Gerhardt , Jacob Roger Haartsen , Cornelis Bernardus Aloysius Wouters , Jan Henrik Poesse
Abstract: The present disclosure relates to a wear-out assessment system including a patient interface for delivering a flow of breathable gas to an airway of a patient, wherein the patient interface includes a first wireless communication unit a communication device including a second wireless communication unit configured to wirelessly communicate with the first wireless communication unit and a wear-out assessment unit for determining wear-out data relating to a wear-out of the patient interface. The first and second wireless communication unit are configured to exchange at least parts of the wear-out data. The present disclosure also relates to a method of assessing wear-out of a patient interface.
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公开(公告)号:US10960183B2
公开(公告)日:2021-03-30
申请号:US16308510
申请日:2017-06-28
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Cornelis Gerardus Maria De Haas , Johannus Gerardus Van Beek , Rudolf Maria Jozef Voncken , Jacob Roger Haartsen , Franciscus Reinier Antonius Van Der Linde , Franciscus Johannes Gerardus Hakkens
Abstract: A deflectable device (100) comprising an elongate body (110) and a folded elongate member (120) is configured to change an orientation of the distal portion (114) of the elongate body (110) with respect to the proximal portion (112) of the elongate body (110) upon an electrical current flowing through the folded elongate member (120) causing a change of a length of the folded elongate member (120).
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4.
公开(公告)号:US20150209540A1
公开(公告)日:2015-07-30
申请号:US14405063
申请日:2013-06-06
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Cornelis Petrus Hendriks , Susanne Maaike Valster , Marc Matysek , Sander Theodoor Pastoor , Roland Alexander Van De Molengraaf , Nicolaas Petrus Willard , Richard Johannus Maria Van De Ven , Joyce Van Zanten , Willem Potze , Sima Asvadi , Rudolf Maria Jozef Voncken , Jacob Roger Haartsen , Mareike Klee , Matthew John Lawrenson , Julian Charles Nolan
CPC classification number: A61M16/0622 , A61M16/0003 , A61M16/0605 , A61M16/0633 , A61M16/0683 , A61M2016/0661 , A61M2205/0266 , A61M2205/0283 , A61M2205/15 , A61M2205/332 , A61M2205/3368 , A61M2230/06 , A61M2230/30 , A61M2230/005
Abstract: The present invention relates to a patient interface and a patient interface system comprising a responsive material and a method for preventing the formation of red marks due to wearing a patient interface (10) that is pressing against the skin of a patient (14) for a longer time and/or for reducing air leakages of the patient interface (10) that may result from an unintended shift of the patient interface (10) on the patient's face. The responsive material is configured for alternating the pressure exerted by the cushion element (18, 26) on the patient (14), and/or the area on the patient where the pressure is exerted by the cushion element in response to a physical quantity acting on the responsive material. The formation of red marks and of air leakages can be reduced or even avoided by means of the responsive material.
Abstract translation: 本发明涉及一种患者接口和患者接口系统,其包括响应材料和用于防止由于佩戴患者接口(10)而形成红色痕迹的方法,所述患者界面(10)压在患者(14)的皮肤上以用于 更长的时间和/或用于减少可能由患者接口(10)在患者面部上的意外移动而导致的患者接口(10)的空气泄漏。 响应材料构造成用于将由衬垫元件(18,26)施加的患者(14)施加的压力和/或患者的区域响应于物理量作用而被缓冲元件施加的压力 对响应材料。 红色痕迹和空气泄漏的形成可以通过响应材料减少甚至避免。
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公开(公告)号:US10532172B2
公开(公告)日:2020-01-14
申请号:US14401279
申请日:2013-05-07
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Rudolf Maria Jozef Voncken , Cornelis Petrus Hendriks , Nicolaas Petrus Willard , Mareike Klee , Joyce Van Zanten , Jacob Roger Haartsen , Willem Potze , Sima Asvadi
IPC: A61M16/06
Abstract: A patient interface device uses a pressure flap which extends inwardly from an outer edge of a mask of the device. The pressure flap is for contacting the skin of the patient to provide a seal or partial seal between the mask volume and the ambient surroundings. The pressure flap includes a cavity area which is exposed to a reduced pressure compared to the mask volume. This assists in keeping the pressure flap pressed against the patient's skin, and thereby maintain a large contact area. This in turn gives a reduction in local high pressure areas.
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公开(公告)号:US09987462B2
公开(公告)日:2018-06-05
申请号:US15318730
申请日:2015-06-01
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Jacob Roger Haartsen , Martinus Bernardus Van Der Mark , Franciscus Johannes Gerardus Hakkens , Maurice Hubertus Elisabeth Van Der Beek
CPC classification number: A61M25/0043 , A61B1/00078 , A61F2/95 , A61M25/0158 , A61M25/09041 , A61M2025/0064 , A61M2025/09158
Abstract: An elongated device includes an optical fiber arranged to allow transmission of light to phase change material arranged long the elongated device, for optically heating the phase change material to change its stiffness from one stiffness value to a different stiffness value. Using distributed tilted or blazed Bragg gratings with light wavelength dependent unique grating periods along the optical fiber, a guide wire or catheter is provided which can be stiffness controlled at selected longitudinal portions. Behavior of the tip of a guide wire or catheter is controlled for optimal navigation. Portions of phase change material arranged inside a tube material can be activated at selected longitudinal parts of the elongated device.
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公开(公告)号:US20160256228A1
公开(公告)日:2016-09-08
申请号:US15027739
申请日:2014-09-30
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Jacob Roger Haartsen , Gert Wim 'T Hooft , Maurice Hubertus Elisabeth Van Der Beek , Franciscus Johannes Gerardus Hakkens
CPC classification number: A61B34/30 , A61B18/1492 , A61B34/20 , A61B2017/00323 , A61B2017/00867 , A61B2017/00871 , A61B2018/00267 , A61B2018/00357 , A61B2018/00577 , A61B2034/2055 , A61B2034/2061 , A61B2034/2063 , A61B2034/301 , A61B2090/062 , A61B2090/064 , A61M25/0141 , A61M25/0158 , A61M2025/0058 , A61M2025/0161 , A61M2025/0166
Abstract: The invention relates to an interventional system (1) for performing an interventional procedure. An interventional instrument (5) like a catheter comprises a bendable portion (12), which is bendable by a bending element (11), and an OSS fiber (10) for generating OSS signals being indicative of the degree of bending of the bendable portion. The actual degree of bending of the bendable portion is determined based on the generated OSS signals and the bending element is controlled depending on the actual determined degree of bending. By using OSS, the actual real degree of bending of the bendable portion of the interventional instrument can very accurately be determined. Moreover, since the bending element is controlled based on this very accurately determined degree of bending, the control of the bending element and, thus, of the interventional instrument can be very accurately.
Abstract translation: 本发明涉及一种用于执行介入手术的介入系统(1)。 诸如导管的介入式器械(5)包括可弯曲元件(11)可弯曲的可弯曲部分(12)和用于产生OSS信号的OSS纤维(10),其指示可弯曲部分的弯曲程度 。 可弯曲部分的实际弯曲程度是根据生成的OSS信号确定的,并且根据实际确定的弯曲程度来控制弯曲元件。 通过使用OSS,可以非常准确地确定介入器械的可弯曲部分的实际实际弯曲度。 此外,由于基于非常精确地确定的弯曲程度来控制弯曲元件,所以可以非常精确地控制弯曲元件以及因此的介入器械的控制。
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公开(公告)号:US20150265795A1
公开(公告)日:2015-09-24
申请号:US14401279
申请日:2013-05-07
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Rudolf Maria Jozef Voncken , Cornelis Petrus Hendriks , Nicolaas Petrus Willard , Mareike Klee , Joyce Van Zanten , Jacob Roger Haartsen , Willem Potze , Sima Asvadi
IPC: A61M16/06
CPC classification number: A61M16/0622 , A61M16/06 , A61M16/0611 , A61M16/0616 , A61M16/0655 , A61M16/0683 , A61M2205/0238
Abstract: A patient interface device uses a pressure flap which extends inwardly from an outer edge of a mask of the device. The pressure flap is for contacting the skin of the patient to provide a seal or partial seal between the mask volume and the ambient surroundings. The pressure flap comprises a cavity area which is exposed to a reduced pressure compared to the mask volume. This assists in keeping the pressure flap pressed against the patient's skin, and thereby maintain a large contact area. This in turn gives a reduction in local high pressure areas.
Abstract translation: 患者接口装置使用从装置的掩模的外边缘向内延伸的压力瓣。 压力瓣片用于接触患者的皮肤以在掩模体积和周围环境之间提供密封或部分密封。 压力片包括与面罩体积相比暴露于减压的空腔区域。 这有助于保持压力皮瓣压靠患者的皮肤,从而保持大的接触面积。 这反过来又降低了当地的高压区域。
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9.
公开(公告)号:US11089998B2
公开(公告)日:2021-08-17
申请号:US15574598
申请日:2016-05-11
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Mareike Klee , Jacob Roger Haartsen , Mark Steven Aloia , Richard Andrew Sofranko , David Smith
Abstract: A device and method for increasing a patient's compliance with a therapy relating to an upper airway disorder includes a receiving unit, a processing unit, and a display unit. The receiving unit is configured to receive vital sign data including glucose level data of the patient, and therapy data including information regarding the therapy of the patient. The processing unit is configured to process the therapy data and the vital sign data in order to determine feedback information based on the therapy data and the vital sign data. Lastly, the display unit is configured to display the feedback information based on the therapy data and the vital sign data.
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公开(公告)号:US10046131B2
公开(公告)日:2018-08-14
申请号:US14405063
申请日:2013-06-06
Applicant: KONINKLIJKE PHILIPS N.V.
Inventor: Cornelis Petrus Hendriks , Susanne Maaike Valster , Marc Matysek , Sander Theodoor Pastoor , Roland Alexander Van De Molengraaf , Nicolaas Petrus Willard , Richard Johannus Maria Van De Ven , Joyce Van Zanten , Willem Potze , Sima Asvadi , Rudolf Maria Jozef Voncken , Jacob Roger Haartsen , Mareike Klee , Matthew John Lawrenson , Julian Charles Nolan
Abstract: A patient interface and a patient interface system comprise a responsive material and a method for preventing the formation of red marks due to wearing a patient interface that is pressing against the skin of a patient for a longer time and/or for reducing air leakages of the patient interface that may result from an unintended shift of the patient interface on the patient's face. The responsive material is configured for alternating the pressure exerted by the cushion element on the patient and/or the area on the patient where the pressure is exerted by the cushion element in response to a physical quantity acting on the responsive material. The formation of red marks and of air leakages can be reduced or even avoided by means of the responsive material.
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