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公开(公告)号:US20220168151A1
公开(公告)日:2022-06-02
申请号:US17583505
申请日:2022-01-25
Applicant: ConvaTec Technologies Inc.
Inventor: David DEWITT , Jonathan VEAL
Abstract: A method of manufacturing a laminated dressing that includes providing a lower layer having a fiber material that directly contacts a patient's skin and a wound area, providing an upper layer that has a foam or foam-like material that absorbs exudate and moisture, and binding the fiber-based lower layer and the foam-based upper layer with a binder layer comprising a binder material, the binder layer including a series of perforations. The perforations in the binder layer are formed by removing material from the binder layer with a pattern coated adhesive sheet prior to binding the fiber-based lower layer and the foam-based upper layer.
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公开(公告)号:US11286601B2
公开(公告)日:2022-03-29
申请号:US16806255
申请日:2020-03-02
Applicant: CONVATEC TECHNOLOGIES INC.
Inventor: Wayne Lee Bonnefin , Lucy Louisa Ballamy , Sarah Wroe , David Parsons , Garry Storey , Joseph Thompson
IPC: A61F13/00 , D06B1/00 , D01F2/24 , D21H13/02 , D01G15/00 , B65B55/02 , A61L15/28 , D04H1/46 , D06M13/278 , A61L15/42 , D06M13/21 , D06M11/38 , D04H1/4258 , A61F13/02 , D06M101/06
Abstract: A chemically modified cellulosic fibre or filament having a moisture content of at least 7% by weight obtained by a process comprising the steps of (i) obtaining cellulosic fibres or filament and chemically modifying the cellulose by substitution to increase its absorbency; (ii) washing the fibres after step (i) in a mixture comprising water and up to 99% by weight of water-miscible organic solvent; (iii) drying the fibres to a moisture content of at least 7% by weight.
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公开(公告)号:US20220087850A1
公开(公告)日:2022-03-24
申请号:US17534550
申请日:2021-11-24
Applicant: ConvaTec Technologies Inc.
Inventor: Mingliang Lawrence Tsai , Tinh Nguyen-Demary
Abstract: Certain embodiments relate to a soft odor barrier material in a medical device. The soft odor barrier material includes an elastomer and an antiblocking agent. In certain forms, the antiblocking agent imparts an interior rough surface having an arithmetic mean surface roughness (Ra) not less than 0.1 μm. In certain forms, the antiblocking agent is non-blocking upon folding and packaging.
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公开(公告)号:US20210369938A1
公开(公告)日:2021-12-02
申请号:US17399271
申请日:2021-08-11
Applicant: CONVATEC TECHNOLOGIES INC.
Inventor: Landy Toth
IPC: A61M1/00 , A61B5/1455 , A61B5/00
Abstract: An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.
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公开(公告)号:US20210369937A1
公开(公告)日:2021-12-02
申请号:US17398552
申请日:2021-08-10
Applicant: Convatec Technologies Inc.
Inventor: Landy Toth
IPC: A61M1/00 , A61B5/1455 , A61B5/00
Abstract: An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.
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公开(公告)号:US11071640B2
公开(公告)日:2021-07-27
申请号:US14646003
申请日:2013-11-20
Applicant: ConvaTec Technologies Inc.
Inventor: George Fattman , Kimberly Murray , Marc Lesko , Thomas Harrit , Nicolani Sorensen
Abstract: Provided herein are controlled evacuation devices, ostomy devices, methods for the manufacture of such devices and the use of such devices.
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公开(公告)号:US10780200B2
公开(公告)日:2020-09-22
申请号:US13992623
申请日:2011-12-07
Applicant: Landy Toth
Inventor: Landy Toth
Abstract: An apparatus (10) for controlling flow of fluid from a wound site of a patient may include a chamber (28) connectable to a wound site and a reservoir (16). The chamber (28) may have a first deformed state, and a second state in which it is not deformed or less deformed than in the first state. The chamber (28) may be adapted to manage fluid flow between the wound site and the reservoir (16) during transition of the chamber (28) between the first state and the second state. An actuator element (64) of the apparatus (10) may be adapted to operate on the chamber (28) to transition the chamber (28) from the second state to the first state.
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公开(公告)号:US10772755B2
公开(公告)日:2020-09-15
申请号:US14451243
申请日:2014-08-04
Applicant: CONVATEC TECHNOLOGIES INC.
Inventor: Christopher C. Gregory
Abstract: The end of the elongated tubular element of the appliance that is designed to be inserted into a body cavity is formed entirely of soft, compliant material. That end carries an inflatable balloon made of non-expandable material, formed in the fully inflated shape, to prevent overexpansion. The balloon is inflated to a predetermined low pressure level to prevent pressure necrosis in the adjacent tissue. A method and apparatus for introducing the soft end of the appliance into the body cavity are also provided. The introducer apparatus includes rigid core surrounded by a soft, compliant sleeve. The sleeve extends beyond the rigid core to form an invertable section. The soft end of the appliance is situated adjacent the apparatus, the balloon is wrapped around the apparatus, and the sleeve section is inverted over the appliance, compressing the balloon and forming a soft, rounded insertion tip. The unit is then introduced into the body cavity. After the appliance is separated from the apparatus, the apparatus is withdrawn.
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公开(公告)号:US10739352B2
公开(公告)日:2020-08-11
申请号:US12743633
申请日:2008-11-20
Applicant: Philip Godfrey Bowler , Samantha Alison Jones , Sarah Anne Welsby
Abstract: A method of diagnosis or prediction of infection of a mammalian wound, said method comprising the step of detecting the presence of a cytokine selected from the group comprising procalcitonin, amino procalcitonin (N-ProCT), eotaxin, granulocyte macrophage colony stimulating factor (GM-CSF), interleukins IB monocyte chemotactic protein-1 (MCP-1), macrophage inflammatory protein-1 alpha (MIP-1a), regulated upon activation normal T expressed and secreted (RANTES) in fluid taken from the wound. Also claimed is the device for use in the method.
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公开(公告)号:US10709825B2
公开(公告)日:2020-07-14
申请号:US15353608
申请日:2016-11-16
Applicant: ConvaTec Technologies Inc.
Inventor: Landy Aaron Toth
IPC: A61M1/00 , A61B5/145 , A61B5/1455 , A61B5/00 , A61B5/01
Abstract: A stand-alone system for assessing wound exudates from the wound of a patient is described. The system contains functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may also compare detected physiological values to predetermined physiological values, in order to obtain a comparison result in real time. The system may include a processor (15) which provides an electronic signal based on the comparison result in which the electronic signal may corresponds to guidelines for treating the wound (3). The system described may be an accessory, which may be used on its own, or in conjunction with other wound treatment devices (9).
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