WO2005104776A2 - Appareil de stabilisation d'un tube - Google Patents

Appareil de stabilisation d'un tube Download PDF

Info

Publication number
WO2005104776A2
WO2005104776A2 PCT/US2005/014572 US2005014572W WO2005104776A2 WO 2005104776 A2 WO2005104776 A2 WO 2005104776A2 US 2005014572 W US2005014572 W US 2005014572W WO 2005104776 A2 WO2005104776 A2 WO 2005104776A2
Authority
WO
WIPO (PCT)
Prior art keywords
restraining device
tube
securing
base
securing members
Prior art date
Application number
PCT/US2005/014572
Other languages
English (en)
Other versions
WO2005104776A3 (fr
Inventor
Edward Walsh
Vicki Johnson
Original Assignee
The Uab Research Foundation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Uab Research Foundation filed Critical The Uab Research Foundation
Publication of WO2005104776A2 publication Critical patent/WO2005104776A2/fr
Publication of WO2005104776A3 publication Critical patent/WO2005104776A3/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/1414—Hanging-up devices
    • A61M5/1418—Clips, separators or the like for supporting tubes or leads
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/84—Drainage tubes; Aspiration tips
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A61M2025/024—Holding devices, e.g. on the body having a clip or clamp system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/02—Holding devices, e.g. on the body
    • A61M2025/0266—Holding devices, e.g. on the body using pads, patches, tapes or the like

Definitions

  • the present disclosure relates generally to the field of devices for holding and securing articles. In one embodiment, the present disclosure relates to devices for holding and securing medical articles.
  • tubes for temporary therapy include, but are not limited to, nasogastric tubing for suction and/or feeding, indwelling urethral catheters, intravenous tubing, chest tubes, and various tubes for drainage.
  • tubes for permanent therapy include, but are not limited to, percutaneous endogastrostomy tubes, indwelling Foley catheters, a suprapublic indwelling catheter and oxygen tubing. All of these tubes, regardless of therapeutic intent, can be cumbersome to the patient with respect to ambulation, activities of daily living (ADLs), and comfort.
  • unsecured tubing can present a hazard in the case of unintentional removal and/or displacement (referred to herein as a "displacement event"), as well as being a contributing factor to falls due to tubing becoming tangled around the patient's feet, or nearby objects.
  • Consequences of inadvertent tube removal include, but are not limited to, infection, bleeding, and costly procedures for replacement.
  • Healthcare providers presently use a variety of methods to secure medical tubing to a patient. Adhesive tape is commonly used for this purpose. However, adhesive tape has a number of disadvantages. First of all adhesive tape is only effective to secure tubing and similar devices for short period of time.
  • adhesive tapes are not waterproof, meaning the tubing is not secured when the patient is exposed to moisture (such as may be the case when bathing or when the adhesive is exposed to perspiration).
  • Adhesive tapes often remove a layer of the skin during such processes and may create an abraded area or a wound. This may cause patient discomfort and may be a source of infection.
  • adhesive tape may not secure the medical tubing in place even though the adhesive tape remains bonded to the skin. Such a situation may occur as a result of movement of the patient and/or the tubing such that the adhesive tape fails to secure the tubing.
  • the forces applied to the patient and or the tubing are transmitted via the tubing to the insertion site for the tubing. This can result in irritation to the insertion site and/or cause a displacement event, with ramifications as discussed above.
  • FIG. 1A is a perspective view of one embodiment of a retaining device as described herein comprising a two securing members.
  • FIG. IB is a perspective view of one embodiment of a single securing member.
  • FIG. 2A is a perspective view of an alternate embodiment of the retaining device in the form of an array comprising a plurality of securing members.
  • FIG. 2B shows one embodiment of a custom designed retaining device having a configuration of securing members derived from the array of FIG. 2A as used on a patient to secure a feeding tube.
  • FIG. 3A is a perspective view of an alternate embodiment of a custom designed retaining device having a configuration of securing members derived from the array of FIG. 2A as used on a patient to secure a feeding tube and further comprising a motion restraint.
  • FIG. 3B is a frontal view of one embodiment of the motion restraint.
  • tubing is meant to include any device or apparatus with a hollow interior, having either a circular or non-circular cross section, that functions as a passage.
  • the tube may be used to transport a variety of solutions, including, but not limited to, liquids, gels, suspensions, emulsions and the like; a solution may comprise a solid component.
  • the tubing may be medical tubing.
  • Exemplary types of medical tubing include, but not limited to, nasogastric tubing for suction and/or feeding, indwelling urethral catheters, intravenous tubing, chest tubes, various tubes for drainage, percutaneous endogastrostomy tubes, indwelling Foley catheters, a suprapublic indwelling catheter and oxygen tubing.
  • any medical tubing whether now in use or used in the future, may be used with the retaining device disclosed.
  • the retaining device can be designed for use with tubing of various sizes and cross sections, rendering it suitable for use in multiple applications including, but not limited to, feeding and intravenous tubing.
  • the retaining device may be used alone or in combinations and/or modular configurations as described in more detail herein, with the advantages inherent in such modular configurations being also described herein.
  • the retaining device described can be used to secure tubing of a variety of lengths, sizes and cross sections.
  • the retaining device can be used in the in-home care setting, in nursing homes, and in hospital settings.
  • the modular placement of the retaining devices in a number of locations as desired allows for securing of any lengths of tubing in any desired configuration.
  • certain tube materials can stiffen with prolonged positioning in a single configuration, the ability to reconfigure the tube path will prolong the life of the tube, resulting in less frequent tube replacement procedures.
  • FIG. 1A shows one embodiment of a retaining device as disclosed.
  • the basic structure described for the retaining device is also applicable to the retaining devices described in modular configurations.
  • the retaining device 1 comprises a base portion 10, which further comprises an upper side 14 and a lower side 12.
  • the lower side 12 may further comprise a medical adhesive 15 as described below and a removable cover 13 for the medical adhesive (not shown).
  • the base portion 10 may be manufactured from a variety of materials. In one embodiment, the base is manufactured from a plastic or a rubber material.
  • Suitable plastics and rubbers include, but are not limited to, materials such as silicone, fluorosilicone, latex rubber, polyvinylchloride, polycarbonate, polypropylene, polyurethane, acetal resin, cflex resin, polyethylene terephthalate, thermoplastic elastomers, nylon, polysulfone, polyaryletherketone, polyesters, etc.
  • the plastic selected exhibits chemical resistance to solvents and is also non- allergenic.
  • the plastic or rubber material selected may be soft and flexible.
  • the base is manufactured from a semi-permeable polyurethane film comprising an adhesive colloidal material.
  • the adhesive colloidal material may be waterproof, allowing the patient to bathe with the retaining devices in position without changing. This minimizes the cost of application as well as any irritation that may develop after prolonged use.
  • the colloidal material does not contain chemicals or compounds such as latex that may induce an allergic reaction in the patient.
  • the base 10 may further comprise a protective cover 40 placed over the base 10. The protective cover may aid in the stabilization of the retaining devices.
  • the protective cover 40 may be manufactured from the materials described above. In one embodiment, the protective cover 40 is manufactured from the same material as the base 10.
  • the upper side 14 of base 10 further comprises at least one securing member 16 mounted on upper side 14.
  • the at least one securing member 16 may extend into the base 10 or may be secured to the upper side 14 of base 10 (such as by protective cover 40).
  • the securing member 16 comprises a central portion 18 (as shown in FIG. IB). Extending upwardly from and in communication with central portion 18 are a plurality of arm members, illustrated in this example as arm members 20A and 20B.
  • the arm members 20A and 20B each have a curved surface 22, a distal end 24 and a proximal end 26.
  • the proximal ends 26 are in communication with opposite sides of the central portion 18.
  • the curved surfaces 22 of the arm members 20A and 20B form a channel 28 with a diameter Z to receive a tubing 30, (not shown in FIGS 1A and B), which in one embodiment is medical tubing.
  • the diameter Z is selected based on the diameter of the tubing to be secured.
  • the diameter Z is such that the arm members 20A and 20B provide sufficient pressure to secure tubing 30 in place without constricting the flow of solution through tube 30.
  • the diameter Z can be increased or decreased by altering the width B of central portion 18 and/or by altering the curvature of the curved surfaces 22 in the arm members 20A and 20B.
  • the securing member 16 may be manufactured as a one piece unit.
  • the securing member 16 may be manufactured in more than one piece and assembled to form the finished unit.
  • arm members 20A and 20B may comprise a gripping element 32 along at least a portion of their length to help secure the tubing 30 in place.
  • the gripping element 32 may be a ridge or a protrusion extending away from the curved surface of said arm members in the direction of the channel 28 (See FIG. IB).
  • at least a portion of the interior portions of the arm members 20A and/or 20B may comprise a non-skid surface, said non-skid surface comprising the gripping element 32.
  • At least a portion of the interior portions of the arm members 20A and or 20B may comprise an adhesive, said adhesive comprising the gripping element 32.
  • the arm members may further comprise a pinch portion 34.
  • the pinch portion 34 is in communication with the distal end 24 of each of the arm members 20A and B.
  • the function of the sloping segments 34 is to allow the securing member to be opened easily to allow the insertion of the tubing 30.
  • the base 10 may be manufactured so as to have a variety of colors or design configurations. The different color or design configurations on the base 10 may create a more aesthetically pleasing appearance to the retaining device 1. This may be especially desirable feature when young children are the patients utilizing the retaining device 1.
  • the design configurations are animals, a logo (a logo may be any recognizable figure representing a group or entity, such as, but not limited to, a professional sports team, a performing group or a corporatio) theme characters, such as cartoon characters, fairy tale characters and the like, landscape scenes, various patterns (such as geometric patterns) and similar designs as is known in the art.
  • the base 10 may comprise one or more colors in various patterns.
  • the colors and design configurations may be combined.
  • the arm members 20A and 20B may also be constructed from a variety of materials. In one embodiment, the arm members are manufactured from a flexible plastic. The use of a flexible plastic allows repeated tube removal and reattachment.
  • the retaining device 1 may comprise one securing member 16 or a plurality of securing members 16.
  • a plurality of the securing members 16 are placed on the base 10 in the form of a pre-fabricated array 100 (shown in FIG. 2A).
  • the base 10 of the array 100 is constructed as described above and has an upper side 14 and a lower side 12, with the lower side 12 further comprising a medical adhesive 15 and removable cover 13 (as described below).
  • the upper side 14 comprises a plurality of securing members (all indicated by the reference numeral 16) secured thereto.
  • the securing members 16 may extend into the base 12 or may be secured to the upper side 14 of base 12 as described above.
  • the securing members 16 may have the structure described above and as shown in FIG. IB.
  • the plurality of securing members 16 is arranged in a pre-determined pattern.
  • the spacing of the securing members 16 on the array 100 is not critical to the present invention and can be varied as desired by varying the distances X and Y in FIG. 2A.
  • X is 1 inch and Y is 1 inch.
  • each X and Y is the same between each securing member 16 (referred to as an ordered array).
  • one or both of the X and Y distances are different at least two of the individual securing members 16 (referred to as a non-ordered array).
  • the securing members 16 are attached to the base 10 over a sufficiently large area to prevent the weight of the tube 30 and/or applied force to the tube 30 from dislocating the retaining device 1 from the skin.
  • the number of securing members 16 in each array 100 can be varied by increasing or decreasing the dimensions of the base 10 containing the array 100 or by changing the values of X and/or Y for a base 10 of a given dimension.
  • the array 100 as shown as a 7 x 9 array, with both X and Y being 1 inch apart.
  • the orientation of the securing members 16 in relation to one another in the array 100 may be uniform or may be non-uniform. In the embodiment shown in FIG.
  • the orientation of the securing members is generally uniform, meaning the orientation of each securing member 16 is the same with respect to one another. However, it should be considered within the scope of the disclosure to provide one or more securing members 16 so that they are in a different orientation with at least one other securing member 16 in the array (see lower left and right hand corners of array 100 in FIG. 2A). Such non-uniform placement may be useful when a user desires to create a custom configuration that requires a change in direction of the tubing (such as an L-shape).
  • the uniform and non-uniform placement of the retaining devices 16 can be used with an ordered array or a non-ordered array.
  • the retaining device 1 may be used in a variety of combinations.
  • Various custom configurations of the retaining device 1 may be constructed from the array 100 shown in FIG. 2A. These custom configurations may contain multiple securing members 16 or may comprise a single securing member. Additionally, a plurality of custom configurations of the retaining device 1 may be used in conjunction with one another when desired. The various custom configurations of the retaining device 1 may be used as desired to provide optimal securing of the desired tubing. Using such custom configurations of the retaining device 1, a user can create a number of custom arrangements of securing members 16 for use in a specific application. Therefore, the retaining device 1 can be custom tailored to provide for securing medical tubes for any needed application. As shown in FIG. 2A, a portion of the array 100 of retaining device 1 has been outlined.
  • a user may cut the array 100 so as to prepare a custom arrangement of securing members 16 on the retaining device 1.
  • the desired, custom arrangement of securing members (indicated as 100A and 100B) is adhered to the skin of the patient 150 in the desired locations as shown in FIG. 2B.
  • the securing members 16 of the retaining device 1 are used to secure a percutaneous endogastric feeding tube (designated 30) both near the site of insertion 152 and near the filling end 154 to stabilize the tubing in order to prevent inadvertent removal or partial removal of the tube 30. Additionally, the configuration secures the tube against the patient to permit normal wearing of clothing.
  • FIG. 30 percutaneous endogastric feeding tube
  • FIG. 3 A shows an alternate embodiment of the retaining device 1.
  • the securing members 16 of the retaining device 1 are used to secure a percutaneous endogastric feeding tube (designated 30) both near the site of insertion 152 and near the filling end 154 to stabilize the tubing as described in FIG. 2B.
  • the retaining device 1 further comprises a motion restraint 50.
  • the motion restraint 50 serves to reversibly engage the tubing 30 secured by the securing members 16 and is placed on the portion of tubing 30 between two of said securing members 16. In use, the motion restraint 50 serves to prevent the unwanted movement of the tubing 30 by limiting the motion of tubing 30.
  • the motion restraint 50 comprises an outer member 52, said outer members comprising a slit 54 along its long axis to allow its placement over and reversible engagement of the tubing (FIG. 3B).
  • the diameter of the outer member 52 may be selected based on the diameter of the tubing. The motion restraint 50 engages the tubing snugly to prevent movement of the tubing along the long axis of the motion restraint 50, but not so snugly as to interfere with the passage of solution inside the tubing.
  • the interior of the outer member 52 comprises a gripping element 56 to aid in the gripping of tubing.
  • the gripping element may be a ridge or protrusion extending from the interior surface of the outer member into the interior of the outer member.
  • the outer member may be cylindrical. Other shapes for the outer member are possible, with a cylindrical configuration being shown for illustrative purposes only.
  • the motion restrain 50 comprises an adjustable flap, strap or similar structure (designated 60) secured to the base between any two of said securing members 16. At least a portion of the interior portion of strap 60 may comprise a gripping element as described above.
  • the gripping element may be a ridge or a protrusion on said interior surface, a non-skid surface, or an adhesive.
  • the strap 60 may be manufactured from any material desired.
  • the strap 60 is manufactured from a non-latex containing material.
  • a specific example of a retaining device 1 having a non-ordered array is disclosed.
  • at least two of the retaining members 16 of the retaining device have an X and/or Y distance that is different from the average X and/or Y distance between the remaining securing members 16.
  • at least two of the retaining members 16 of the retaining device have an X and/or Y distance that is less than the average X and/or Y distance between the remaining securing members 16.
  • the securing members 16 having the different X and/or Y distances may be placed on the restraining device 1 in one corner of the array 100, in more than one corner of the array 100, in the center of the array 100, or any combination of the foregoing. Other locations on the array 100 may also be used.
  • the closely spaced configuration of securing members 16 on the restraining device 16 may be useful for placement near or adjacent to the site of insertion of the tube 30 or near or adjacent to other areas of the tube 30 in need of additional restraint.
  • the medical adhesive used in the present disclosure can be any medical adhesive currently in use. In one embodiment, the medical adhesive is non-allergenic and can be used repeatedly without irritation to the skin of the patient. In one embodiment, the medical adhesive is a hydro-colloidal adhesive.
  • the hydro-colloidal adhesive presents the advantage of repelling water to the extent that showering and sweating do not degrade the integrity of the adhesive bond, as demonstrated by placement of a restraining devices described herein in excess of 14 days for securing a percutaneous endogastrostomy tube.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Anesthesiology (AREA)
  • Public Health (AREA)
  • Vascular Medicine (AREA)
  • Biophysics (AREA)
  • Pulmonology (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • External Artificial Organs (AREA)
  • Materials For Medical Uses (AREA)

Abstract

L'invention concerne un dispositif de retenue permettant de fixer un tube. Dans un mode de réalisation, ledit dispositif de retenue comprend une base et un élément de fixation, et sert à fixer un tube médical à un patient afin d'éviter tout traumatisme pour le patient ou un retrait du tube par inadvertance. Ledit dispositif de retenue peut également comprendre un adhésif médical permettant de fixer le dispositif de retenue au patient sur l'emplacement désiré. Le dispositif de retenue peut également être fourni sous forme d'un réseau comprenant une pluralité d'éléments de fixation permettant à l'utilisateur d'utiliser la configuration désirée pour fixer le tube médical.
PCT/US2005/014572 2004-04-27 2005-04-27 Appareil de stabilisation d'un tube WO2005104776A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US56599404P 2004-04-27 2004-04-27
US60/565,994 2004-04-27

Publications (2)

Publication Number Publication Date
WO2005104776A2 true WO2005104776A2 (fr) 2005-11-10
WO2005104776A3 WO2005104776A3 (fr) 2009-04-23

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010093798A1 (fr) * 2009-02-12 2010-08-19 Becton, Dickinson And Company Systèmes et procédés d'organisation et d'amorçage d'un ensemble d'administration intraveineuse
EP2501429A1 (fr) * 2009-11-18 2012-09-26 Bioderm, Inc. Porte-tube et procédé de fixation de cathéters sur un patient
WO2014174238A1 (fr) * 2013-04-24 2014-10-30 Keymed (Medical & Industrial Equipment) Limited Tapis comprenant des doigts permettant de saisir un tube de cathéter
WO2015020882A1 (fr) * 2013-08-05 2015-02-12 3M Innovative Properties Company Dispositif de fixation de cathéter
US10105899B2 (en) 2015-03-26 2018-10-23 Becton, Dickinson And Company IV membrane attachment systems and methods
US10201667B2 (en) 2015-03-26 2019-02-12 Becton, Dickinson And Company IV membrane attachment systems and methods
US10232130B2 (en) 2015-03-26 2019-03-19 Becton, Dickinson And Company Anti-run dry membrane
US10369332B2 (en) 2009-11-18 2019-08-06 Bioderm, Inc. Interlocking low profile gripping device
US10485955B2 (en) 2009-11-18 2019-11-26 Bioderm, Inc. Securement device for polymer tubing and polymer coated cables
US10646648B2 (en) 2015-04-01 2020-05-12 Becton, Dickinson And Company IV flow management systems and methods
US10702689B2 (en) 2015-03-26 2020-07-07 Becton, Dickinson And Company Auto-stop vent plug
US11266813B2 (en) 2017-04-10 2022-03-08 Bioderm, Inc. Interlocking low profile gripping device

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US4220016A (en) * 1976-02-27 1980-09-02 Frenger Rita K Skin jewelry
US6324435B1 (en) * 2000-06-22 2001-11-27 Ethicon, Inc. Electrical connector for cardiac devices
US6585196B2 (en) * 2001-05-30 2003-07-01 Newfrey Llc Fastener for pipe or the like
US6708931B2 (en) * 2002-01-22 2004-03-23 Nifco Inc. Clamp and fixing method for tubular object

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US4220016A (en) * 1976-02-27 1980-09-02 Frenger Rita K Skin jewelry
US6324435B1 (en) * 2000-06-22 2001-11-27 Ethicon, Inc. Electrical connector for cardiac devices
US6585196B2 (en) * 2001-05-30 2003-07-01 Newfrey Llc Fastener for pipe or the like
US6708931B2 (en) * 2002-01-22 2004-03-23 Nifco Inc. Clamp and fixing method for tubular object

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102355912A (zh) * 2009-02-12 2012-02-15 贝克顿·迪金森公司 用于排布和排气充注静脉输液组件的系统和方法
US8282046B2 (en) 2009-02-12 2012-10-09 Becton, Dickinson And Company Systems and methods for organizing and priming an IV administration set
AU2010213705B2 (en) * 2009-02-12 2015-11-12 Becton, Dickinson And Company Systems and methods for organizing and priming an IV administration set
WO2010093798A1 (fr) * 2009-02-12 2010-08-19 Becton, Dickinson And Company Systèmes et procédés d'organisation et d'amorçage d'un ensemble d'administration intraveineuse
EP2501429A1 (fr) * 2009-11-18 2012-09-26 Bioderm, Inc. Porte-tube et procédé de fixation de cathéters sur un patient
EP2501429A4 (fr) * 2009-11-18 2013-05-22 Bioderm Inc Porte-tube et procédé de fixation de cathéters sur un patient
US11376402B2 (en) 2009-11-18 2022-07-05 Bioderm, Inc. Securement device for polymer tubing and polymer coated cables
US10485955B2 (en) 2009-11-18 2019-11-26 Bioderm, Inc. Securement device for polymer tubing and polymer coated cables
US10369332B2 (en) 2009-11-18 2019-08-06 Bioderm, Inc. Interlocking low profile gripping device
WO2014174238A1 (fr) * 2013-04-24 2014-10-30 Keymed (Medical & Industrial Equipment) Limited Tapis comprenant des doigts permettant de saisir un tube de cathéter
US10441749B2 (en) 2013-08-05 2019-10-15 3M Innovative Properties Company Catheter securement device
WO2015020882A1 (fr) * 2013-08-05 2015-02-12 3M Innovative Properties Company Dispositif de fixation de cathéter
US10232130B2 (en) 2015-03-26 2019-03-19 Becton, Dickinson And Company Anti-run dry membrane
US10201667B2 (en) 2015-03-26 2019-02-12 Becton, Dickinson And Company IV membrane attachment systems and methods
US10702689B2 (en) 2015-03-26 2020-07-07 Becton, Dickinson And Company Auto-stop vent plug
US10926029B2 (en) 2015-03-26 2021-02-23 Becton, Dickinson And Company IV membrane attachment systems and methods
US10973993B2 (en) 2015-03-26 2021-04-13 Becton, Dickinson And Company Anti-run dry membrane
US10105899B2 (en) 2015-03-26 2018-10-23 Becton, Dickinson And Company IV membrane attachment systems and methods
US11744941B2 (en) 2015-03-26 2023-09-05 Becton, Dickinson And Company IV membrane attachment systems and methods
US11826557B2 (en) 2015-03-26 2023-11-28 Becton, Dickinson And Company Anti-run dry membrane
US10646648B2 (en) 2015-04-01 2020-05-12 Becton, Dickinson And Company IV flow management systems and methods
US11617831B2 (en) 2015-04-01 2023-04-04 Becton, Dickinson And Company IV flow management systems and methods
US11266813B2 (en) 2017-04-10 2022-03-08 Bioderm, Inc. Interlocking low profile gripping device

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