WO2021124727A1 - Medical connector - Google Patents

Medical connector Download PDF

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Publication number
WO2021124727A1
WO2021124727A1 PCT/JP2020/041765 JP2020041765W WO2021124727A1 WO 2021124727 A1 WO2021124727 A1 WO 2021124727A1 JP 2020041765 W JP2020041765 W JP 2020041765W WO 2021124727 A1 WO2021124727 A1 WO 2021124727A1
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WO
WIPO (PCT)
Prior art keywords
rotating member
medical device
medical
lock cylinder
connector
Prior art date
Application number
PCT/JP2020/041765
Other languages
French (fr)
Japanese (ja)
Inventor
俊彦 柿木
Original Assignee
テルモ株式会社
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 テルモ株式会社 filed Critical テルモ株式会社
Publication of WO2021124727A1 publication Critical patent/WO2021124727A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/02Access sites
    • A61M39/04Access sites having pierceable self-sealing members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/10Tube connectors; Tube couplings

Definitions

  • This disclosure relates to medical connectors.
  • an infusion line is formed using a medical tube or the like, and a liquid such as a drug solution is supplied into the body through this infusion line.
  • Medical devices such as medical tubes and syringes used in infusion lines are connected to each other using medical connectors.
  • the medical connector partitions the first flow path and connects to the first medical device, the first connection portion, and the second flow path that communicates with the first flow path, and is connected to the second medical device. It has a second connection part.
  • the medical connector may have a first rotating member provided with a first connecting portion and a second rotating member rotatably connected to the first rotating member about an axis and having a second connecting portion.
  • the first connection portion is reversibly connected to the first medical device by rotating in the first circumferential direction about the axis of the first medical device. May be configured to be. According to such a configuration, the connection state at the first connection portion can be maintained satisfactorily.
  • the first rotating member has a grip portion that is gripped by a finger for a connection operation and a separation operation with respect to the first medical device. Therefore, if a medical worker, a patient, or the like erroneously operates the grip portion, the first connection portion may be unintentionally separated from the first medical device.
  • an object of the present disclosure is to provide a medical connector that can maintain a good connection state at the first connection portion and is unlikely to be separated at the first connection portion due to an erroneous operation.
  • the medical connector as one aspect of the present disclosure includes a first rotating member and a second rotating member connected to the first rotating member via a rotation transmission mechanism, and the first rotating member is a first rotating member. It has a first connection portion that is reversibly connected to the first medical device by partitioning one flow path and rotating in the first circumferential direction about an axis with respect to the first medical device, and the second rotation.
  • the member has a second connecting portion that partitions the second flow path communicating with the first flow path and is reversibly connected to the second medical device, and the rotation transmission mechanism is the second rotating member. Restricts the first rotating member from rotating in the first circumferential direction, while the second rotating member has a second circumference that is opposite to the first rotating member in the first circumferential direction. Allowing rotation in the direction, the second rotating member covers the first rotating member so that the first rotating member cannot be gripped in a state where the first connecting portion is connected to the first medical device. It has a covering part.
  • the first medical device has a male connector portion and a lock cylinder located radially outside the male connector portion, and the first connection portion has the male connector portion. It has a female connector portion to be inserted, and the outer peripheral surface of the female connector portion is reversibly connected to the lock cylinder by engaging the concave-convex shapes with each other by rotating in the first circumferential direction with respect to the lock cylinder. Has an engaging part.
  • the first rotating member includes an outer wall forming a part of the rotation transmission mechanism and has an outer portion located radially outside the female connector portion, and the covering portion. Covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
  • a gap having a size of 6 mm or less in a direction along the axis is provided between the covering portion and the lock cylinder. Is formed.
  • the first medical device has a female connector portion
  • the first connection portion has a male connector portion inserted into the female connector portion and a radial outer side of the male connector portion.
  • the inner peripheral surface of the lock cylinder is rotated in the first circumferential direction with respect to the female connector portion, so that the concave-convex shapes are engaged with each other and the female connector portion is reversibly engaged with the female connector portion. It has an engaging part to be connected.
  • the first rotating member includes an outer wall forming a part of the rotation transmission mechanism and the lock cylinder, and has an outer portion located radially outside the male connector portion. Then, the covering portion covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
  • the second medical device is reversibly connected to the second connection portion by rotating about the axis with respect to the second connection portion.
  • the second medical device is reversibly connected to the second connection portion by rotating in the first circumferential direction with respect to the second connection portion.
  • the second connection portion has a valve body that closes the second flow path.
  • the second medical device has a male connector portion
  • the second connection portion has a female connector portion having an insertion port into which the male connector portion is inserted, and the valve body.
  • the male connector portion opens by pushing the closed portion into the second flow path from the insertion port.
  • the second medical device has a male connector portion and a lock cylinder located radially outside the male connector portion, and the second connecting portion has the male connector portion. It has a female connector portion to be inserted, and the outer peripheral surface of the female connector portion becomes the lock cylinder by engaging the concave-convex shapes with each other by rotating the lock cylinder with respect to the female connector portion in the first circumferential direction. It has an engaging part that is reversibly connected.
  • FIG. 1 It is a perspective view which shows the medical connector as 1st Embodiment. It is a vertical sectional view of the medical connector shown in FIG. It is a perspective view which shows the 1st rotating member of the medical connector shown in FIG. It is sectional drawing in the cross section along the circumferential direction which shows the ratchet mechanism of the rotation transmission mechanism of the medical connector shown in FIG. It is a vertical cross-sectional view which shows the state when the 1st connection part of the medical connector shown in FIG. 1 is connected to the 1st medical device. It is a vertical cross-sectional view which shows the state when the 2nd connection part is connected to the 2nd medical device in the state where the 1st connection part of the medical connector shown in FIG. 1 is connected to the 1st medical device. It is an external view which shows the infusion set including the medical connector shown in the figure. It is a vertical sectional view which shows the medical connector as a 2nd Embodiment.
  • FIGS. 1 to 8 The corresponding elements in each figure are designated by the same reference numerals.
  • the medical connector 1 according to the first embodiment shown in FIGS. 1 to 3 has a first rotating member 2 and a second rotating member 4 connected to the first rotating member 2 via a rotation transmission mechanism 3. doing.
  • the first rotating member 2 partitions the first flow path 5 and rotates in the first circumferential direction C1 about the axis O with respect to the first medical device 6 (see FIG. 5) to cover the first medical device 6. It has a first connecting portion 7 that is reversibly connected to the connecting portion 6a.
  • the second rotating member 4 is a second connecting portion that partitions the second flow path 8 that communicates with the first flow path 5 and is reversibly connected to the connected portion 9a of the second medical instrument 9 (see FIG. 6).
  • the second connecting portion 10 has a valve body 11 that closes the second flow path 8. That is, the second connection portion 10 is configured as a closed type connection portion. However, the second connection portion 10 is not limited to this, and may be configured as an open type connection portion that does not have a valve body 11 that closes the second flow path 8.
  • the first connection portion 7 is configured as an open type connection portion that does not have a valve body that closes the first flow path 5. However, the first connecting portion 7 is not limited to this, and may be configured as a closed type connecting portion having a valve body that closes the first flow path 5.
  • the first connecting portion 7 is connected to the connected portion 6a of the first medical instrument 6 by rotating in the first circumferential direction C1 with respect to the first medical instrument 6, and is connected to the connected portion 6a of the first medical instrument 6 in the first circumferential direction C1 with respect to the first medical instrument 6.
  • the second circumferential direction C2 which is the opposite direction of the above, the first medical device 6 is separated from the connected portion 6a. That is, the first connecting portion 7 is reversibly connected to the connected portion 6a of the first medical device 6 by rotating in the first circumferential direction C1 with respect to the first medical device 6.
  • the rotation transmission mechanism 3 regulates the second rotating member 4 from rotating in the first circumferential direction C1 with respect to the first rotating member 2, while the second rotating member 4 is second with respect to the first rotating member 2. It is configured to allow rotation in the circumferential direction C2.
  • the direction along the axis O is referred to as the axial direction A
  • the direction from the second connecting portion 10 to the first connecting portion 7 along the axial direction A is referred to as the first axial direction A1 or downward
  • the first axial direction A1 is referred to as the second axial direction A2 or upward
  • the direction orbiting the axis O is referred to as the circumferential direction C
  • the direction perpendicular to the axis O is referred to as the radial direction (not shown), and includes the axis O.
  • the cross section is called the vertical cross section.
  • the direction that is clockwise (clockwise) when viewed in the first axial direction A1 is defined as the first circumferential direction C1, but the present invention is not limited to this. That is, the direction that is counterclockwise (counterclockwise) when viewed in the first axial direction A1 may be the first circumferential direction C1.
  • the connected portion 9a of the second medical device 9 rotates about the axis O with respect to the second connecting portion 10, that is, rotates in the circumferential direction C, so that the connected portion 9a is reversible to the second connecting portion 10. It is configured to be connected to.
  • the connected portion 9a of the second medical device 9 is not limited to this, and for example, the second connecting portion 10 moves in the first axial direction A1 with respect to the second connecting portion 10 without rotation in the circumferential direction C. It may be configured to be reversibly connected to.
  • the connected portion 9a of the second medical device 9 is configured to be reversibly connected to the second connecting portion 10 by rotating in the first circumferential direction C1 with respect to the second connecting portion 10.
  • the connected portion 9a of the second medical device 9 is not limited to this, and is reversibly connected to the second connecting portion 10 by rotating in the second circumferential direction C2 with respect to the second connecting portion 10, for example. It may be configured.
  • the connected portion 9a of the second medical device 9 has a male connector portion 9b and a lock cylinder 9c located radially outside the male connector portion 9b, but is not limited to this.
  • the second connection portion 10 has a female connector portion 12 into which the male connector portion 9b is inserted, but is not limited to this.
  • the outer peripheral surface of the female connector portion 12 is an engaging portion 13 that is reversibly connected to the lock cylinder 9c by engaging the concave-convex shapes with each other by rotating the lock cylinder 9c with respect to the female connector portion 12 in the first circumferential direction C1.
  • the locking cylinder 9c rotates in the second circumferential direction C2 with respect to the engaging portion 13, so that the engaging portion 13 is reversible to the lock cylinder 9c due to the engagement between the uneven shapes. It may be configured to be connected to.
  • the engagement between the concave-convex shapes between the engaging portion 13 and the lock cylinder 9c is screwed, but is not limited to this.
  • the second connection portion 10 is configured to comply with, for example, ISO 80369-7 of 2016.
  • the female connector portion 12 has an insertion port 14 into which the male connector portion 9b is inserted.
  • the valve body 11 is an elastic valve body having a disc-shaped closing portion 11b that closes the insertion port 14 and has a slit 11a, and a fixing portion 11c that is connected to the outer peripheral edge of the closing portion 11b and is fixed to the insertion port 14. Is.
  • the slit 11a is configured so that the male connector portion 9b opens by pushing the closing portion 11b into the second flow path 8 from the insertion port 14.
  • the configuration of the valve body 11 is not limited to this.
  • the second rotating member 4 includes a tubular inner cylinder 15 centered on the axis O, a flange 16 extending radially outward from the upper end of the inner cylinder 15, and a flange 16 downward from the outer peripheral edge of the flange 16. It has a tubular outer cylinder 17 extending upward, a tubular female connector portion 12 centered on an axis O extending upward from the flange 16, and a valve body 11, but the present invention is not limited to this.
  • the housing 4a composed of the inner cylinder 15, the flange 16, the outer cylinder 17, and the female connector portion 12 is composed of three members, an upper cap 18, a lower cap 19, and a holder 20.
  • the housing 4a is not limited to this, and may be composed of, for example, two or less members, or may be composed of four or more members.
  • the upper cap 18, the lower cap 19, and the holder 20 are each formed by, for example, injection molding, but are not limited thereto.
  • the upper cap 18, the lower cap 19 and the holder 20 are joined by, for example, fusion.
  • the housing 4a is made of, for example, a synthetic resin
  • the valve body 11 is made of, for example, rubber or an elastomer.
  • An upper wall 21 extending inward in the radial direction is connected to the upper portion of the inner peripheral surface of the inner cylinder 15, and the upper wall 21 has a through hole 22 penetrating in the vertical direction.
  • a hollow portion 23 is formed between the through hole 22 and the valve body 11.
  • the second flow path 8 is composed of a hollow portion 23 and a through hole 22, but is not limited to this.
  • the connected portion 6a of the first medical device 6 has a male connector portion 6b and a lock cylinder 6c located radially outside the male connector portion 6b, but is limited to this. Absent.
  • the first connection portion 7 has a female connector portion 24 into which the male connector portion 6b is inserted, but the first connection portion 7 is not limited to this.
  • the outer peripheral surface of the female connector portion 24 has an engaging portion 25 that is reversibly connected to the lock cylinder 6c by engaging the concave-convex shapes with each other by rotating in the first circumferential direction C1 with respect to the lock cylinder 6c.
  • the engagement between the concave-convex shapes between the engaging portion 25 and the lock cylinder 6c is screwed, but is not limited to this.
  • the first connection unit 7 is configured to comply with, for example, ISO 80369-7 of 2016.
  • the first rotating member 2 has a tubular shape centered on the axis O and is located at the inner portion 26 constituting the female connector portion 24 and radially outside the female connector portion 24. It has a housing 2a provided with an outer portion 27 to be formed, but is not limited to this.
  • the outer portion 27 has an annular wall 28 extending radially outward from the inner portion 26 and a tubular outer wall 29 centered on an axis O extending upward from the annular wall 28 and forming a part of the rotation transmission mechanism 3.
  • the first rotating member 2 is made of, for example, a synthetic resin.
  • the first rotating member 2 is formed by, for example, injection molding.
  • the inner peripheral surface of the inner portion 26 partitions the first flow path 5.
  • the upper part of the inner portion 26 is inserted into the inner cylinder 15.
  • the upper part of the inner part 26 and the part below the upper wall 21 on the inner peripheral surface of the inner cylinder 15 are in close contact with each other, so that the connection portion between the first flow path 5 and the second flow path 8 is formed.
  • a close portion 30 is formed to prevent liquid leakage.
  • the close portion 30 between the inner portion 26 and the inner cylinder 15 may be provided in a portion different from this.
  • An annular elastic member centered on the axis O may be provided between the inner portion 26 and the inner cylinder 15 to ensure closer sealing by the elastic member.
  • the rotation transmission mechanism 3 has a rotation connecting portion 3a that rotatably connects the housing 2a of the first rotation member 2 and the housing 4a of the second rotation member 4 in the circumferential direction C. Further, the rotation transmission mechanism 3 restricts the second rotating member 4 from rotating in the first circumferential direction C1 with respect to the first rotating member 2, while the second rotating member 4 has a second with respect to the first rotating member 2. It has a ratchet mechanism 3b that allows rotation in the two circumferential directions C2.
  • the rotary connecting portion 3a is composed of an engaging portion 31 between the outer wall 29 and the inner cylinder 15 inserted into the outer wall 29, but is not limited to this.
  • the engaging portion 31 is composed of an annular groove 32 provided on the outer peripheral surface of the inner cylinder 15 and a plurality of claws 33 provided on the outer wall 29, but is not limited thereto.
  • the number of claws 33 is not limited to a plurality.
  • the ratchet mechanism 3b is composed of a plurality of convex portions 34 arranged at intervals in the circumferential direction C and a deformable portion 35 that can be elastically deformed.
  • the deformed portion 35 hits one of the convex portions 34 to prevent the rotation, while the second rotating member 4 causes the second rotating member 4.
  • the convex portion 34 is elastically deformed (see the two-dot chain line in FIG. 4) so as to get over the convex portion 34 in the second circumferential direction C2.
  • the deformed portion 35 is provided in the housing 2a of the first rotating member 2, and the convex portion 34 is provided in the housing 4a of the second rotating member 4, but the present invention is not limited to this. That is, the deformed portion 35 may be provided in the housing 2a of the first rotating member 2, and the convex portion 34 may be provided in the housing 4a of the second rotating member 4.
  • the deformed portion 35 is provided on the upper surface of the outer wall 29, and the convex portion 34 is provided on the lower surface of the flange 16, but the present invention is not limited to this.
  • the deformed portion 35 may be provided on the lower surface of the flange 16, and the convex portion 34 may be provided on the upper surface of the outer wall 29.
  • the deformed portion 35 is composed of a cantilever elastic piece, but is not limited to this.
  • the deformed portion 35 has a fixed end in the first circumferential direction C1 and a free end in the second circumferential direction C2, but is not limited to this.
  • the second rotating member 4 rotates first so that the first rotating member 2 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6.
  • It has a covering portion 36 that covers the member 2. More specifically, the covering portion 36 is configured to cover the outer portion 27 so that the outer portion 27 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6.
  • the distance D (see FIG. 2) in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is, for example, -3 mm or more.
  • the covering portion 36 is composed of a part of the housing 4a of the second rotating member 4. More specifically, the covering portion 36 is composed of an outer cylinder 17, but is not limited to this.
  • a gap G having a size of 6 mm or less in the axial direction A is provided between the covering portion 36 and the lock cylinder 6c of the first medical instrument 6. (See FIG. 5) is formed.
  • the medical connector 1 can be used as follows in, for example, an infusion line formed when performing infusion, blood transfusion, artificial dialysis, or the like.
  • the first connection portion 7 of the medical connector 1 is connected to the connected portion 6a of the first medical device 6.
  • the male connector portion 6b of the first medical instrument 6 is inserted into the female connector portion 24 of the first connection portion 7 of the medical connector 1, and in this state, the first rotating member 2 is locked to the first medical instrument 6. This is done by rotating the cylinder 6c in the first circumferential direction C1.
  • one hand grips the lock cylinder 6c of the first medical device 6 and the other hand grips the cover portion 36 of the first rotating member 2, and the cover portion 36 is attached to the lock cylinder 6c. It is performed by the operation of rotating in the first circumferential direction C1. At this time, since the rotation transmission mechanism 3 rotates the second rotating member 4 together with the first rotating member 2, the engaging portion 25 of the female connector portion 24 can be connected to the lock cylinder 6c.
  • the connection state at the first connection portion 7 can be maintained satisfactorily. Further, since the second connection portion 10 of the medical connector 1 is closed by the valve body 11, the first connection portion 7 of the medical connector 1 is connected to the connected portion 6a of the first medical instrument 6. It is possible to maintain a state in which the connected portion 6a of the medical device 6 is closed by the medical connector 1.
  • the rotation transmission mechanism 3 makes the second rotating member 4 the first rotating member 2. Let it spin freely. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated from each other.
  • the covering portion 36 of the second rotating member 4 covers the first rotating member 2 so that the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the first rotating member 2.
  • the covering portion 36 covers the outer portion 27 of the first rotating member 2 so that the outer portion 27 of the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the outer portion 27. Further, when the distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is -3 mm or more, such an effect can be obtained more reliably.
  • a gap G having a size of 6 mm or less is formed in the axial direction A between the covering portion 36 and the lock cylinder 6c of the first medical instrument 6.
  • the female connector portion 24 cannot be gripped through the gap G. Therefore, it is possible to prevent the first connection portion 7 of the medical connector 1 from being separated from the connected portion 6a of the first medical device 6 due to an erroneous operation of the first connection portion 7 to the female connector portion 24.
  • the connected portion 9a of the second medical instrument 9 is connected to the second connecting portion 10 of the medical connector 1 as needed.
  • the first medical device 6 and the second medical device 9 can be connected to each other via the medical connector 1.
  • the male connector portion 9b of the second medical instrument 9 is inserted into the female connector portion 12 of the second connection portion 10 of the medical connector 1, and in this state, the lock cylinder 9c of the second medical instrument 9 is rotated for the first time. This is done by rotating the member 2 in the first circumferential direction C1.
  • one hand grips the covering portion 36 of the second rotating member 4 (not shown), and the other hand grips the lock cylinder 9c of the second medical device 9 to cover the lock cylinder 9c. It is performed by the operation of rotating the 36 in the first circumferential direction C1.
  • the second connecting portion 10 rotates together with the lock cylinder 9c. Since this is restricted by the rotation transmission mechanism 3, the lock cylinder 9c can be connected to the second connection portion 10.
  • the medical connector 1 may be used without being separated from the first medical device 6 for the period of use of the first medical device 6 after being once connected to the first medical device 6, or may be used for separation.
  • a tool may be provided so that it can be separated from the first medical device 6 by using the jig if necessary.
  • FIG. 7 shows an example of an infusion set 37 for forming an infusion line.
  • the infusion set 37 shown in FIG. 7 is used to form an infusion line connecting an infusion holder such as an infusion bag (not shown) to an indwelling needle (not shown).
  • the infusion set 37 includes a first medical device 6 configured as a first medical tube, a medical connector 1, a second medical device 9 configured as a second medical tube, and an intravenous drip tube. It has 38, an adjusting clamp 39, and a closing clamp 40.
  • the drip tube 38 makes the flow rate of the infusion solution supplied from the infusion solution holder visible.
  • the adjusting clamp 39 can change the flow rate of the infusion agent in the infusion line to a plurality of states.
  • the occluding clamp 40 can occlude the infusion line.
  • the distal end of the first medical device 6 is directly or indirectly connected to the proximal end of the indwelling needle.
  • a connected portion 6a connected to the first connecting portion 7 of the medical connector 1 is provided.
  • a connected portion 9a connected to the second connecting portion 10 of the medical connector 1 is provided.
  • the proximal end of the second medical device 9 is connected to the distal end of the infusion tube 38.
  • the proximal end of the second medical device 9 is directly connected to the distal end of the infusion tube 38, but may be indirectly connected.
  • the proximal end of the drip tube 38 is directly or indirectly connected to the infusion holder.
  • the infusion set 37 is not limited to the configuration having the first medical device 6, the medical connector 1, the second medical device 9, the drip tube 38, the adjusting clamp 39 and the closing clamp 40, for example, the first medical device 6, medical treatment. It may be configured to have a clamp 1 and a second medical device 9.
  • the connected portion 6a of the first medical device 6 has a male connector portion 6b and a lock cylinder 6c, and the first connecting portion 7 of the medical connector 1 has a female connector portion 24. ..
  • the connected portion 6a of the first medical device 6 has the female connector portion 6d, and the first connecting portion 7 of the medical connector 1 has the male connector portion 41.
  • a lock cylinder 42 may be provided.
  • the first connection portion 7 has the male connector portion 41 inserted into the female connector portion 6d of the connected portion 6a of the first medical device 6 and the male connector portion 41 in the radial direction with respect to the male connector portion 41. It has a lock cylinder 42 located on the outside. The inner peripheral surface of the lock cylinder 42 has an engaging portion 43 that is reversibly connected to the female connector portion by engaging the concave-convex shapes with each other by rotating in the first circumferential direction C1 with respect to the female connector portion 6d. There is.
  • the engagement between the concave-convex shapes between the female connector portion 6d and the engaging portion 43 of the lock cylinder 42 is screwed, but is not limited to this.
  • the first connection unit 7 is configured to comply with, for example, ISO 80369-7 of 2016.
  • the first rotating member 2 includes an outer wall 29 and a lock cylinder 42 that form a part of the rotation transmission mechanism 3, and also has an outer portion 27 that is located radially outside the male connector portion 41.
  • the covering portion 36 is configured to cover the outer portion 27 so that the outer portion 27 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6.
  • the covering portion 36 is configured to cover the first rotating member 2 so that the first rotating member 2 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6.
  • the distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is, for example, -3 mm or more.
  • the covering portion 36 is composed of a part of the housing 4a of the second rotating member 4. More specifically, the covering portion 36 is composed of an outer cylinder 17, but is not limited to this.
  • the medical connector 1 according to the second embodiment can be used, for example, in the infusion set 37 in the same manner as in the case of the first embodiment.
  • the connection at the first connection portion 7 is made by reversibly connecting the first connection portion 7 to the connected portion 6a of the first medical instrument 6 by a rotation operation. The condition can be maintained in good condition.
  • the covering portion 36 of the second rotating member 4 covers the first rotating member 2 so that the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the first rotating member 2.
  • the covering portion 36 covers the outer portion 27 of the first rotating member 2 so that the outer portion 27 of the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the outer portion 27. Further, when the distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is -3 mm or more, such an effect can be obtained more reliably.
  • the medical connector according to the present disclosure is not limited to the configuration of the above embodiment, and can be appropriately changed within the scope of the claims.

Abstract

This medical connector comprises a first rotation member and a second rotation member which is coupled to the first rotation member via a rotation transmitting mechanism. The first rotation member has a first connection part which is reversibly connected to a first medical tool by being rotated in a first circumferential direction relative to the first medical tool, and the second rotation member has a second connection member which is reversibly connected to a second medical tool. The rotation transmitting mechanism regulates rotation of the second rotation member in the first circumferential direction relative to the first rotation member while allowing rotation of the second rotation member in a second circumferential direction relative to the first rotation member. The second rotation member has a cover part that covers the first rotation member so as to prevent the first rotation member from being held when the first connection member is connected to the first medical tool.

Description

医療用コネクタMedical connector
 本開示は、医療用コネクタに関する。 This disclosure relates to medical connectors.
 従来から、輸液、輸血、人工透析などを行う場合に、医療用チューブ等を用いて輸液ラインを形成し、この輸液ラインを通じて体内に薬液等の液体を供給している。輸液ラインにおいて使用される医療用チューブ、シリンジ等の医療器具は、医療用コネクタを用いて互いに接続される。医療用コネクタは、第1流路を区画するとともに第1医療器具に接続される第1接続部と、第1流路と連通する第2流路を区画するとともに第2医療器具に接続される第2接続部とを有している。 Conventionally, when performing infusion, blood transfusion, artificial dialysis, etc., an infusion line is formed using a medical tube or the like, and a liquid such as a drug solution is supplied into the body through this infusion line. Medical devices such as medical tubes and syringes used in infusion lines are connected to each other using medical connectors. The medical connector partitions the first flow path and connects to the first medical device, the first connection portion, and the second flow path that communicates with the first flow path, and is connected to the second medical device. It has a second connection part.
 医療用コネクタは、第1接続部を備える第1回転部材と、第1回転部材に軸線を中心として回転可能に連結されるとともに第2接続部を備える第2回転部材とを有する場合がある。またこの場合において第1接続部は、例えば特許文献1に記載されるように、第1医療器具に対し前記軸線を中心として第1周方向に回転することで第1医療器具に可逆的に接続されるように構成される場合がある。このような構成によれば、第1接続部での接続状態を良好に維持することができる。 The medical connector may have a first rotating member provided with a first connecting portion and a second rotating member rotatably connected to the first rotating member about an axis and having a second connecting portion. Further, in this case, as described in Patent Document 1, for example, the first connection portion is reversibly connected to the first medical device by rotating in the first circumferential direction about the axis of the first medical device. May be configured to be. According to such a configuration, the connection state at the first connection portion can be maintained satisfactorily.
国際公開第2019/130891号International Publication No. 2019/130891
 しかし、特許文献1に記載されるような医療用コネクタでは、第1回転部材は、第1医療器具に対する接続操作と分離操作のために指で把持される把持部を有している。このため、医療従事者や患者等が当該把持部を誤操作した場合には、意図せずに第1接続部が第1医療器具から分離してしまう虞がある。 However, in a medical connector as described in Patent Document 1, the first rotating member has a grip portion that is gripped by a finger for a connection operation and a separation operation with respect to the first medical device. Therefore, if a medical worker, a patient, or the like erroneously operates the grip portion, the first connection portion may be unintentionally separated from the first medical device.
 そこで本開示は、第1接続部での接続状態を良好に維持できるとともに誤操作による第1接続部での分離が生じ難い医療用コネクタを提供することを目的とする。 Therefore, an object of the present disclosure is to provide a medical connector that can maintain a good connection state at the first connection portion and is unlikely to be separated at the first connection portion due to an erroneous operation.
 本開示の一態様としての医療用コネクタは、第1回転部材と、前記第1回転部材に回転伝達機構を介して連結される第2回転部材とを有し、前記第1回転部材は、第1流路を区画するとともに第1医療器具に対し軸線を中心として第1周方向に回転することで前記第1医療器具に可逆的に接続される第1接続部を有し、前記第2回転部材は、前記第1流路と連通する第2流路を区画するとともに前記第2医療器具に可逆的に接続される第2接続部を有し、前記回転伝達機構は、前記第2回転部材が前記第1回転部材に対して前記第1周方向に回転することを規制する一方、前記第2回転部材が前記第1回転部材に対して前記第1周方向の反対方向である第2周方向に回転することを許容し、前記第2回転部材は、前記第1接続部が前記第1医療器具に接続された状態において前記第1回転部材を把持できないように前記第1回転部材を覆う覆い部を有する。 The medical connector as one aspect of the present disclosure includes a first rotating member and a second rotating member connected to the first rotating member via a rotation transmission mechanism, and the first rotating member is a first rotating member. It has a first connection portion that is reversibly connected to the first medical device by partitioning one flow path and rotating in the first circumferential direction about an axis with respect to the first medical device, and the second rotation. The member has a second connecting portion that partitions the second flow path communicating with the first flow path and is reversibly connected to the second medical device, and the rotation transmission mechanism is the second rotating member. Restricts the first rotating member from rotating in the first circumferential direction, while the second rotating member has a second circumference that is opposite to the first rotating member in the first circumferential direction. Allowing rotation in the direction, the second rotating member covers the first rotating member so that the first rotating member cannot be gripped in a state where the first connecting portion is connected to the first medical device. It has a covering part.
 本開示の一実施形態として、前記第1医療器具は、雄コネクタ部と前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、前記第1接続部は、前記雄コネクタ部を挿入される雌コネクタ部を有し、前記雌コネクタ部の外周面は、前記ロック筒に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記ロック筒に可逆的に接続される係合部を有する。 As one embodiment of the present disclosure, the first medical device has a male connector portion and a lock cylinder located radially outside the male connector portion, and the first connection portion has the male connector portion. It has a female connector portion to be inserted, and the outer peripheral surface of the female connector portion is reversibly connected to the lock cylinder by engaging the concave-convex shapes with each other by rotating in the first circumferential direction with respect to the lock cylinder. Has an engaging part.
 本開示の一実施形態として、前記第1回転部材は、前記回転伝達機構の一部を構成する外壁を備えるとともに前記雌コネクタ部よりも径方向外側に位置する外側部分を有し、前記覆い部は、前記第1接続部が前記第1医療器具に接続された状態において、前記外側部分を把持できないように前記外側部分を覆う。 As one embodiment of the present disclosure, the first rotating member includes an outer wall forming a part of the rotation transmission mechanism and has an outer portion located radially outside the female connector portion, and the covering portion. Covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
 本開示の一実施形態として、前記第1接続部が前記第1医療器具に接続された状態において、前記覆い部と前記ロック筒との間に前記軸線に沿う方向に6mm以下の大きさの隙間が形成される。 As one embodiment of the present disclosure, in a state where the first connecting portion is connected to the first medical device, a gap having a size of 6 mm or less in a direction along the axis is provided between the covering portion and the lock cylinder. Is formed.
 本開示の一実施形態として、前記第1医療器具は雌コネクタ部を有し、前記第1接続部は、前記雌コネクタ部に挿入される雄コネクタ部と、前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、前記ロック筒の内周面は、前記雌コネクタ部に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記雌コネクタ部に可逆的に接続される係合部を有する。 As one embodiment of the present disclosure, the first medical device has a female connector portion, and the first connection portion has a male connector portion inserted into the female connector portion and a radial outer side of the male connector portion. The inner peripheral surface of the lock cylinder is rotated in the first circumferential direction with respect to the female connector portion, so that the concave-convex shapes are engaged with each other and the female connector portion is reversibly engaged with the female connector portion. It has an engaging part to be connected.
 本開示の一実施形態として、前記第1回転部材は、前記回転伝達機構の一部を構成する外壁と前記ロック筒とを備えるとともに前記雄コネクタ部よりも径方向外側に位置する外側部分を有し、前記覆い部は、前記第1接続部が前記第1医療器具に接続された状態において、前記外側部分を把持できないように前記外側部分を覆う。 As one embodiment of the present disclosure, the first rotating member includes an outer wall forming a part of the rotation transmission mechanism and the lock cylinder, and has an outer portion located radially outside the male connector portion. Then, the covering portion covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
 本開示の一実施形態として、前記第2医療器具は、前記第2接続部に対し前記軸線を中心として回転することで前記第2接続部に可逆的に接続される。 As one embodiment of the present disclosure, the second medical device is reversibly connected to the second connection portion by rotating about the axis with respect to the second connection portion.
 本開示の一実施形態として、前記第2医療器具は、前記第2接続部に対し前記第1周方向に回転することで前記第2接続部に可逆的に接続される。 As one embodiment of the present disclosure, the second medical device is reversibly connected to the second connection portion by rotating in the first circumferential direction with respect to the second connection portion.
 本開示の一実施形態として、前記第2接続部は前記第2流路を閉塞する弁体を有する。 As one embodiment of the present disclosure, the second connection portion has a valve body that closes the second flow path.
 本開示の一実施形態として、前記第2医療器具は雄コネクタ部を有し、前記第2接続部は、前記雄コネクタ部を挿入される挿入口を備える雌コネクタ部を有し、前記弁体は、前記挿入口を閉塞するとともにスリットを備える円板状の閉塞部と、前記閉塞部の外周縁に連なるとともに前記挿入口に固定される固定部とを有する弾性弁体であり、前記スリットは、前記雄コネクタ部が前記閉塞部を前記挿入口から前記第2流路内に押し込むことにより開口する。 As one embodiment of the present disclosure, the second medical device has a male connector portion, and the second connection portion has a female connector portion having an insertion port into which the male connector portion is inserted, and the valve body. Is an elastic valve body having a disk-shaped closing portion that closes the insertion port and has a slit, and a fixing portion that is connected to the outer peripheral edge of the closing portion and is fixed to the insertion port. , The male connector portion opens by pushing the closed portion into the second flow path from the insertion port.
 本開示の一実施形態として、前記第2医療器具は、雄コネクタ部と前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、前記第2接続部は、前記雄コネクタ部を挿入される雌コネクタ部を有し、前記雌コネクタ部の外周面は、前記ロック筒が前記雌コネクタ部に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記ロック筒に可逆的に接続される係合部を有する。 As one embodiment of the present disclosure, the second medical device has a male connector portion and a lock cylinder located radially outside the male connector portion, and the second connecting portion has the male connector portion. It has a female connector portion to be inserted, and the outer peripheral surface of the female connector portion becomes the lock cylinder by engaging the concave-convex shapes with each other by rotating the lock cylinder with respect to the female connector portion in the first circumferential direction. It has an engaging part that is reversibly connected.
 本開示によれば、第1接続部での接続状態を良好に維持できるとともに誤操作による第1接続部での分離が生じ難い医療用コネクタを提供することができる。 According to the present disclosure, it is possible to provide a medical connector that can maintain a good connection state at the first connection portion and is unlikely to be separated at the first connection portion due to an erroneous operation.
第1実施形態としての医療用コネクタを示す斜視図である。It is a perspective view which shows the medical connector as 1st Embodiment. 図1に示す医療用コネクタの縦断面図である。It is a vertical sectional view of the medical connector shown in FIG. 図1に示す医療用コネクタの第1回転部材を示す斜視図である。It is a perspective view which shows the 1st rotating member of the medical connector shown in FIG. 図1に示す医療用コネクタの回転伝達機構のラチェット機構を示す周方向に沿う断面での断面図である。It is sectional drawing in the cross section along the circumferential direction which shows the ratchet mechanism of the rotation transmission mechanism of the medical connector shown in FIG. 図1に示す医療用コネクタの第1接続部を第1医療器具に接続しているときの様子を示す縦断面図である。It is a vertical cross-sectional view which shows the state when the 1st connection part of the medical connector shown in FIG. 1 is connected to the 1st medical device. 図1に示す医療用コネクタの第1接続部を第1医療器具に接続した状態で第2接続部を第2医療器具に接続しているときの様子を示す縦断面図である。It is a vertical cross-sectional view which shows the state when the 2nd connection part is connected to the 2nd medical device in the state where the 1st connection part of the medical connector shown in FIG. 1 is connected to the 1st medical device. 図に示す医療用コネクタを含む輸液セットを示す外観図である。It is an external view which shows the infusion set including the medical connector shown in the figure. 第2実施形態としての医療用コネクタを示す縦断面図である。It is a vertical sectional view which shows the medical connector as a 2nd Embodiment.
 以下、本開示に係る医療用コネクタの実施形態について、図1~図8を参照して詳細に例示説明する。各図において対応する要素には同一の符号を付している。 Hereinafter, embodiments of the medical connector according to the present disclosure will be illustrated in detail with reference to FIGS. 1 to 8. The corresponding elements in each figure are designated by the same reference numerals.
 図1~図3に示す第1実施形態に係る医療用コネクタ1は、第1回転部材2と、第1回転部材2に回転伝達機構3を介して連結される第2回転部材4とを有している。第1回転部材2は、第1流路5を区画するとともに第1医療器具6(図5参照)に対し軸線Oを中心として第1周方向C1に回転することで第1医療器具6の被接続部6aに可逆的に接続される第1接続部7を有している。第2回転部材4は、第1流路5と連通する第2流路8を区画するとともに第2医療器具9(図6参照)の被接続部9aに可逆的に接続される第2接続部10を有している。「可逆的に接続される」とは、接続のための動作と逆の動作により分離可能に接続されることを意味している。第2接続部10は第2流路8を閉塞する弁体11を有している。つまり第2接続部10は閉塞型接続部として構成されている。しかし第2接続部10はこれに限らず、第2流路8を閉塞する弁体11を有さない開放型接続部として構成してもよい。第1接続部7は第1流路5を閉塞する弁体を有さない開放型接続部として構成されている。しかし第1接続部7はこれに限らず、第1流路5を閉塞する弁体を有する閉塞型接続部として構成してもよい。 The medical connector 1 according to the first embodiment shown in FIGS. 1 to 3 has a first rotating member 2 and a second rotating member 4 connected to the first rotating member 2 via a rotation transmission mechanism 3. doing. The first rotating member 2 partitions the first flow path 5 and rotates in the first circumferential direction C1 about the axis O with respect to the first medical device 6 (see FIG. 5) to cover the first medical device 6. It has a first connecting portion 7 that is reversibly connected to the connecting portion 6a. The second rotating member 4 is a second connecting portion that partitions the second flow path 8 that communicates with the first flow path 5 and is reversibly connected to the connected portion 9a of the second medical instrument 9 (see FIG. 6). Has 10. "Reversibly connected" means that the connection is separable by the operation opposite to the operation for connection. The second connecting portion 10 has a valve body 11 that closes the second flow path 8. That is, the second connection portion 10 is configured as a closed type connection portion. However, the second connection portion 10 is not limited to this, and may be configured as an open type connection portion that does not have a valve body 11 that closes the second flow path 8. The first connection portion 7 is configured as an open type connection portion that does not have a valve body that closes the first flow path 5. However, the first connecting portion 7 is not limited to this, and may be configured as a closed type connecting portion having a valve body that closes the first flow path 5.
 第1接続部7は、第1医療器具6に対し第1周方向C1に回転することで第1医療器具6の被接続部6aに接続され、第1医療器具6に対し第1周方向C1の反対方向である第2周方向C2に回転することで第1医療器具6の被接続部6aから分離する。つまり、第1接続部7は、第1医療器具6に対し第1周方向C1に回転することで第1医療器具6の被接続部6aに可逆的に接続される。 The first connecting portion 7 is connected to the connected portion 6a of the first medical instrument 6 by rotating in the first circumferential direction C1 with respect to the first medical instrument 6, and is connected to the connected portion 6a of the first medical instrument 6 in the first circumferential direction C1 with respect to the first medical instrument 6. By rotating in the second circumferential direction C2, which is the opposite direction of the above, the first medical device 6 is separated from the connected portion 6a. That is, the first connecting portion 7 is reversibly connected to the connected portion 6a of the first medical device 6 by rotating in the first circumferential direction C1 with respect to the first medical device 6.
 回転伝達機構3は、第2回転部材4が第1回転部材2に対して第1周方向C1に回転することを規制する一方、第2回転部材4が第1回転部材2に対して第2周方向C2に回転することを許容するように構成されている。 The rotation transmission mechanism 3 regulates the second rotating member 4 from rotating in the first circumferential direction C1 with respect to the first rotating member 2, while the second rotating member 4 is second with respect to the first rotating member 2. It is configured to allow rotation in the circumferential direction C2.
 本実施形態では、軸線Oに沿う方向を軸方向Aといい、軸方向Aに沿って第2接続部10から第1接続部7に向かう方向を第1軸方向A1又は下方といい、第1軸方向A1の反対方向を第2軸方向A2又は上方といい、軸線Oを周回する方向を周方向Cといい、軸線Oに垂直な方向を径方向(図示省略)といい、軸線Oを含む断面を縦断面という。 In the present embodiment, the direction along the axis O is referred to as the axial direction A, and the direction from the second connecting portion 10 to the first connecting portion 7 along the axial direction A is referred to as the first axial direction A1 or downward, and the first The direction opposite to the axial direction A1 is referred to as the second axial direction A2 or upward, the direction orbiting the axis O is referred to as the circumferential direction C, the direction perpendicular to the axis O is referred to as the radial direction (not shown), and includes the axis O. The cross section is called the vertical cross section.
 また本実施形態では、第1軸方向A1に視たときに右回り(時計回り)となる方向を第1周方向C1としているが、これに限らない。すなわち、第1軸方向A1に視たときに左回り(反時計回り)となる方向を第1周方向C1としてもよい。 Further, in the present embodiment, the direction that is clockwise (clockwise) when viewed in the first axial direction A1 is defined as the first circumferential direction C1, but the present invention is not limited to this. That is, the direction that is counterclockwise (counterclockwise) when viewed in the first axial direction A1 may be the first circumferential direction C1.
 図6に示すように、第2医療器具9の被接続部9aは、第2接続部10に対し軸線Oを中心として回転、つまり周方向Cに回転することで第2接続部10に可逆的に接続されるように構成されている。しかし第2医療器具9の被接続部9aはこれに限らず例えば、第2接続部10に対し、周方向Cの回転を伴わずに第1軸方向A1に移動することで第2接続部10に可逆的に接続されるように構成してもよい。 As shown in FIG. 6, the connected portion 9a of the second medical device 9 rotates about the axis O with respect to the second connecting portion 10, that is, rotates in the circumferential direction C, so that the connected portion 9a is reversible to the second connecting portion 10. It is configured to be connected to. However, the connected portion 9a of the second medical device 9 is not limited to this, and for example, the second connecting portion 10 moves in the first axial direction A1 with respect to the second connecting portion 10 without rotation in the circumferential direction C. It may be configured to be reversibly connected to.
 第2医療器具9の被接続部9aは、第2接続部10に対し第1周方向C1に回転することで第2接続部10に可逆的に接続されるように構成されている。しかし、第2医療器具9の被接続部9aはこれに限らず例えば、第2接続部10に対し第2周方向C2に回転することで第2接続部10に可逆的に接続されるように構成してもよい。 The connected portion 9a of the second medical device 9 is configured to be reversibly connected to the second connecting portion 10 by rotating in the first circumferential direction C1 with respect to the second connecting portion 10. However, the connected portion 9a of the second medical device 9 is not limited to this, and is reversibly connected to the second connecting portion 10 by rotating in the second circumferential direction C2 with respect to the second connecting portion 10, for example. It may be configured.
 第2医療器具9の被接続部9aは、雄コネクタ部9bと雄コネクタ部9bよりも径方向外側に位置するロック筒9cとを有しているが、これに限らない。第2接続部10は、雄コネクタ部9bを挿入される雌コネクタ部12を有しているが、これに限らない。雌コネクタ部12の外周面は、ロック筒9cが雌コネクタ部12に対し第1周方向C1に回転することで凹凸形状同士の係合によってロック筒9cに可逆的に接続される係合部13を有しているが、これに限らない。なお、係合部13及びロック筒9cは、ロック筒9cが係合部13に対し第2周方向C2に回転することで凹凸形状同士の係合によって係合部13がロック筒9cに可逆的に接続されるように構成してもよい。 The connected portion 9a of the second medical device 9 has a male connector portion 9b and a lock cylinder 9c located radially outside the male connector portion 9b, but is not limited to this. The second connection portion 10 has a female connector portion 12 into which the male connector portion 9b is inserted, but is not limited to this. The outer peripheral surface of the female connector portion 12 is an engaging portion 13 that is reversibly connected to the lock cylinder 9c by engaging the concave-convex shapes with each other by rotating the lock cylinder 9c with respect to the female connector portion 12 in the first circumferential direction C1. However, it is not limited to this. In the engaging portion 13 and the lock cylinder 9c, the locking cylinder 9c rotates in the second circumferential direction C2 with respect to the engaging portion 13, so that the engaging portion 13 is reversible to the lock cylinder 9c due to the engagement between the uneven shapes. It may be configured to be connected to.
 係合部13とロック筒9cとの間における凹凸形状同士の係合は螺合であるが、これに限らない。第2接続部10は例えば、2016年のISO80369-7に準拠するように構成される。 The engagement between the concave-convex shapes between the engaging portion 13 and the lock cylinder 9c is screwed, but is not limited to this. The second connection portion 10 is configured to comply with, for example, ISO 80369-7 of 2016.
 雌コネクタ部12は、雄コネクタ部9bを挿入される挿入口14を有している。弁体11は、挿入口14を閉塞するとともにスリット11aを備える円板状の閉塞部11bと、閉塞部11bの外周縁に連なるとともに挿入口14に固定される固定部11cとを有する弾性弁体である。スリット11aは、雄コネクタ部9bが閉塞部11bを挿入口14から第2流路8内に押し込むことにより開口するように構成されている。しかし、弁体11の構成はこれに限らない。 The female connector portion 12 has an insertion port 14 into which the male connector portion 9b is inserted. The valve body 11 is an elastic valve body having a disc-shaped closing portion 11b that closes the insertion port 14 and has a slit 11a, and a fixing portion 11c that is connected to the outer peripheral edge of the closing portion 11b and is fixed to the insertion port 14. Is. The slit 11a is configured so that the male connector portion 9b opens by pushing the closing portion 11b into the second flow path 8 from the insertion port 14. However, the configuration of the valve body 11 is not limited to this.
 図2に示すように、第2回転部材4は、軸線Oを中心とする筒状の内筒15と、内筒15の上端から径方向外側に延びるフランジ16と、フランジ16の外周縁から下方に延びる筒状の外筒17と、フランジ16から上方に延びる軸線Oを中心とする筒状の雌コネクタ部12と、弁体11とを有しているが、これに限らない。 As shown in FIG. 2, the second rotating member 4 includes a tubular inner cylinder 15 centered on the axis O, a flange 16 extending radially outward from the upper end of the inner cylinder 15, and a flange 16 downward from the outer peripheral edge of the flange 16. It has a tubular outer cylinder 17 extending upward, a tubular female connector portion 12 centered on an axis O extending upward from the flange 16, and a valve body 11, but the present invention is not limited to this.
 内筒15、フランジ16、外筒17及び雌コネクタ部12で構成されるハウジング4aは、上キャップ18、下キャップ19及びホルダ20の3つの部材で構成されている。しかしハウジング4aはこれに限らず例えば、2つ以下の部材で構成してもよいし、4つ以上の部材で構成してもよい。上キャップ18、下キャップ19及びホルダ20はそれぞれ、例えば射出成形によって形成されるがこれに限らない。上キャップ18、下キャップ19及びホルダ20は例えば融着によって接合される。ハウジング4aは例えば合成樹脂製であり、弁体11は例えばゴム又はエラストマー製である。 The housing 4a composed of the inner cylinder 15, the flange 16, the outer cylinder 17, and the female connector portion 12 is composed of three members, an upper cap 18, a lower cap 19, and a holder 20. However, the housing 4a is not limited to this, and may be composed of, for example, two or less members, or may be composed of four or more members. The upper cap 18, the lower cap 19, and the holder 20 are each formed by, for example, injection molding, but are not limited thereto. The upper cap 18, the lower cap 19 and the holder 20 are joined by, for example, fusion. The housing 4a is made of, for example, a synthetic resin, and the valve body 11 is made of, for example, rubber or an elastomer.
 内筒15の内周面における上部には、径方向内側に延びる上部壁21が連なっており、上部壁21は上下方向に貫通する貫通孔22を有している。貫通孔22と弁体11との間には、中空部23が形成されている。第2流路8は中空部23と貫通孔22とで構成されているが、これに限らない。 An upper wall 21 extending inward in the radial direction is connected to the upper portion of the inner peripheral surface of the inner cylinder 15, and the upper wall 21 has a through hole 22 penetrating in the vertical direction. A hollow portion 23 is formed between the through hole 22 and the valve body 11. The second flow path 8 is composed of a hollow portion 23 and a through hole 22, but is not limited to this.
 図5に示すように、第1医療器具6の被接続部6aは、雄コネクタ部6bと雄コネクタ部6bよりも径方向外側に位置するロック筒6cとを有しているが、これに限らない。第1接続部7は、雄コネクタ部6bを挿入される雌コネクタ部24を有しているが、これに限らない。雌コネクタ部24の外周面は、ロック筒6cに対し第1周方向C1に回転することで凹凸形状同士の係合によってロック筒6cに可逆的に接続される係合部25を有しているが、これに限らない。 As shown in FIG. 5, the connected portion 6a of the first medical device 6 has a male connector portion 6b and a lock cylinder 6c located radially outside the male connector portion 6b, but is limited to this. Absent. The first connection portion 7 has a female connector portion 24 into which the male connector portion 6b is inserted, but the first connection portion 7 is not limited to this. The outer peripheral surface of the female connector portion 24 has an engaging portion 25 that is reversibly connected to the lock cylinder 6c by engaging the concave-convex shapes with each other by rotating in the first circumferential direction C1 with respect to the lock cylinder 6c. However, it is not limited to this.
 係合部25とロック筒6cとの間における凹凸形状同士の係合は螺合であるが、これに限らない。第1接続部7は例えば、2016年のISO80369-7に準拠するように構成される。 The engagement between the concave-convex shapes between the engaging portion 25 and the lock cylinder 6c is screwed, but is not limited to this. The first connection unit 7 is configured to comply with, for example, ISO 80369-7 of 2016.
 図2、図3に示すように、第1回転部材2は、軸線Oを中心とする筒状であり雌コネクタ部24を構成する内側部分26と、雌コネクタ部24よりも径方向外側に位置する外側部分27とを備えるハウジング2aを有しているが、これに限らない。外側部分27は、内側部分26から径方向外側に延びる環状壁28と、環状壁28から上方に延びる軸線Oを中心とする筒状であり、回転伝達機構3の一部を構成する外壁29とを有しているが、これに限らない。第1回転部材2は例えば合成樹脂製である。第1回転部材2は例えば射出成形によって形成される。 As shown in FIGS. 2 and 3, the first rotating member 2 has a tubular shape centered on the axis O and is located at the inner portion 26 constituting the female connector portion 24 and radially outside the female connector portion 24. It has a housing 2a provided with an outer portion 27 to be formed, but is not limited to this. The outer portion 27 has an annular wall 28 extending radially outward from the inner portion 26 and a tubular outer wall 29 centered on an axis O extending upward from the annular wall 28 and forming a part of the rotation transmission mechanism 3. However, it is not limited to this. The first rotating member 2 is made of, for example, a synthetic resin. The first rotating member 2 is formed by, for example, injection molding.
 内側部分26の内周面は第1流路5を区画している。内側部分26の上部は内筒15に挿入されている。内側部分26の上部と、内筒15の内周面における上部壁21よりも下側の部分とは互いに密接しており、これにより第1流路5と第2流路8との接続部での液漏れを防止する密接部30を形成している。しかし、内側部分26と内筒15との密接部30は、これと異なる部分に設けてもよい。内側部分26と内筒15との間に軸線Oを中心とする環状の弾性部材を設け、当該弾性部材を介した密接により密封性を確保する構成としてもよい。 The inner peripheral surface of the inner portion 26 partitions the first flow path 5. The upper part of the inner portion 26 is inserted into the inner cylinder 15. The upper part of the inner part 26 and the part below the upper wall 21 on the inner peripheral surface of the inner cylinder 15 are in close contact with each other, so that the connection portion between the first flow path 5 and the second flow path 8 is formed. A close portion 30 is formed to prevent liquid leakage. However, the close portion 30 between the inner portion 26 and the inner cylinder 15 may be provided in a portion different from this. An annular elastic member centered on the axis O may be provided between the inner portion 26 and the inner cylinder 15 to ensure closer sealing by the elastic member.
 回転伝達機構3は、第1回転部材2のハウジング2aと第2回転部材4のハウジング4aとを周方向Cに回転可能に連結する回転連結部3aを有している。また回転伝達機構3は、第2回転部材4が第1回転部材2に対して第1周方向C1に回転することを規制する一方、第2回転部材4が第1回転部材2に対して第2周方向C2に回転することを許容するラチェット機構3bを有している。 The rotation transmission mechanism 3 has a rotation connecting portion 3a that rotatably connects the housing 2a of the first rotation member 2 and the housing 4a of the second rotation member 4 in the circumferential direction C. Further, the rotation transmission mechanism 3 restricts the second rotating member 4 from rotating in the first circumferential direction C1 with respect to the first rotating member 2, while the second rotating member 4 has a second with respect to the first rotating member 2. It has a ratchet mechanism 3b that allows rotation in the two circumferential directions C2.
 回転連結部3aは、外壁29と外壁29に挿入された内筒15との係合部31で構成されているが、これに限らない。係合部31は、内筒15の外周面に設けられた環状溝32と、外壁29に設けられた複数の爪33とで構成されているが、これに限らない。なお爪33の数は複数に限らない。 The rotary connecting portion 3a is composed of an engaging portion 31 between the outer wall 29 and the inner cylinder 15 inserted into the outer wall 29, but is not limited to this. The engaging portion 31 is composed of an annular groove 32 provided on the outer peripheral surface of the inner cylinder 15 and a plurality of claws 33 provided on the outer wall 29, but is not limited thereto. The number of claws 33 is not limited to a plurality.
 ラチェット機構3bは、図1~図4に示すように、周方向Cに間隔を空けて並ぶ複数の凸部34と、弾性変形可能な変形部35とで構成されている。なお図1においては1つのみの凸部34に符号を付している。変形部35は、第2回転部材4が第1回転部材2に対して第1周方向C1に回転するときには凸部34の一つに突き当り、当該回転を阻止する一方、第2回転部材4が第1回転部材2に対して第2周方向C2に回転するときには弾性変形(図4中の二点鎖線を参照)して凸部34を第2周方向C2に乗り越えるように構成されている。 As shown in FIGS. 1 to 4, the ratchet mechanism 3b is composed of a plurality of convex portions 34 arranged at intervals in the circumferential direction C and a deformable portion 35 that can be elastically deformed. In FIG. 1, only one convex portion 34 is designated by a reference numeral. When the second rotating member 4 rotates in the first circumferential direction C1 with respect to the first rotating member 2, the deformed portion 35 hits one of the convex portions 34 to prevent the rotation, while the second rotating member 4 causes the second rotating member 4. When rotating in the second circumferential direction C2 with respect to the first rotating member 2, the convex portion 34 is elastically deformed (see the two-dot chain line in FIG. 4) so as to get over the convex portion 34 in the second circumferential direction C2.
 変形部35は第1回転部材2のハウジング2aに設けられ、凸部34は第2回転部材4のハウジング4aに設けられているが、これに限らない。すなわち、変形部35を第1回転部材2のハウジング2aに設け、凸部34を第2回転部材4のハウジング4aに設けてもよい。 The deformed portion 35 is provided in the housing 2a of the first rotating member 2, and the convex portion 34 is provided in the housing 4a of the second rotating member 4, but the present invention is not limited to this. That is, the deformed portion 35 may be provided in the housing 2a of the first rotating member 2, and the convex portion 34 may be provided in the housing 4a of the second rotating member 4.
 変形部35は外壁29の上面に設けられ、凸部34はフランジ16の下面に設けられているが、これに限らない。例えば、変形部35をフランジ16の下面に設け、凸部34を外壁29の上面に設けてもよい。変形部35は片持ちの弾性片で構成されているが、これに限らない。変形部35は第1周方向C1の端部が固定端、第2周方向C2の端部が自由端とされているが、これに限らない。 The deformed portion 35 is provided on the upper surface of the outer wall 29, and the convex portion 34 is provided on the lower surface of the flange 16, but the present invention is not limited to this. For example, the deformed portion 35 may be provided on the lower surface of the flange 16, and the convex portion 34 may be provided on the upper surface of the outer wall 29. The deformed portion 35 is composed of a cantilever elastic piece, but is not limited to this. The deformed portion 35 has a fixed end in the first circumferential direction C1 and a free end in the second circumferential direction C2, but is not limited to this.
 図1、図2、図5に示すように、第2回転部材4は、第1接続部7が第1医療器具6に接続された状態において第1回転部材2を把持できないように第1回転部材2を覆う覆い部36を有している。より具体的に、覆い部36は、第1接続部7が第1医療器具6に接続された状態において、外側部分27を把持できないように外側部分27を覆うように構成されている。外側部分27の下端から覆い部36の下端までの第1軸方向A1の距離D(図2参照)は例えば、-3mm以上である。覆い部36は第2回転部材4のハウジング4aの一部で構成されている。より具体的に、覆い部36は外筒17で構成されているが、これに限らない。 As shown in FIGS. 1, 2, and 5, the second rotating member 4 rotates first so that the first rotating member 2 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6. It has a covering portion 36 that covers the member 2. More specifically, the covering portion 36 is configured to cover the outer portion 27 so that the outer portion 27 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6. The distance D (see FIG. 2) in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is, for example, -3 mm or more. The covering portion 36 is composed of a part of the housing 4a of the second rotating member 4. More specifically, the covering portion 36 is composed of an outer cylinder 17, but is not limited to this.
 第1接続部7が第1医療器具6に接続された状態において、覆い部36と第1医療器具6のロック筒6cとの間には例えば、軸方向Aに6mm以下の大きさの隙間G(図5参照)が形成される。 In a state where the first connecting portion 7 is connected to the first medical instrument 6, for example, a gap G having a size of 6 mm or less in the axial direction A is provided between the covering portion 36 and the lock cylinder 6c of the first medical instrument 6. (See FIG. 5) is formed.
 医療用コネクタ1は例えば、輸液、輸血、人工透析などを行う場合に形成される輸液ラインにおいて次のように使用することができる。まず、図5に示すように、第1医療器具6の被接続部6aに医療用コネクタ1の第1接続部7を接続する。この接続は、第1医療器具6の雄コネクタ部6bを医療用コネクタ1の第1接続部7の雌コネクタ部24に挿入し、この状態で第1回転部材2を第1医療器具6のロック筒6cに対して第1周方向C1に回転させることにより行われる。この接続は例えば、一方の手で第1医療器具6のロック筒6cを把持するとともにもう一方の手で第1回転部材2の覆い部36を把持し、覆い部36をロック筒6cに対して第1周方向C1に回転させる操作によって行われる。このとき回転伝達機構3は第2回転部材4を第1回転部材2に対して共回りさせるので、雌コネクタ部24の係合部25をロック筒6cに接続することができる。 The medical connector 1 can be used as follows in, for example, an infusion line formed when performing infusion, blood transfusion, artificial dialysis, or the like. First, as shown in FIG. 5, the first connection portion 7 of the medical connector 1 is connected to the connected portion 6a of the first medical device 6. In this connection, the male connector portion 6b of the first medical instrument 6 is inserted into the female connector portion 24 of the first connection portion 7 of the medical connector 1, and in this state, the first rotating member 2 is locked to the first medical instrument 6. This is done by rotating the cylinder 6c in the first circumferential direction C1. In this connection, for example, one hand grips the lock cylinder 6c of the first medical device 6 and the other hand grips the cover portion 36 of the first rotating member 2, and the cover portion 36 is attached to the lock cylinder 6c. It is performed by the operation of rotating in the first circumferential direction C1. At this time, since the rotation transmission mechanism 3 rotates the second rotating member 4 together with the first rotating member 2, the engaging portion 25 of the female connector portion 24 can be connected to the lock cylinder 6c.
 このように回転操作によって第1接続部7を第1医療器具6の被接続部6aに可逆的に接続することにより、第1接続部7での接続状態を良好に維持することができる。また医療用コネクタ1の第2接続部10は弁体11で閉塞されているので、第1医療器具6の被接続部6aに医療用コネクタ1の第1接続部7を接続することによって第1医療器具6の被接続部6aを医療用コネクタ1で閉塞した状態を維持することができる。 By reversibly connecting the first connection portion 7 to the connected portion 6a of the first medical device 6 by the rotation operation in this way, the connection state at the first connection portion 7 can be maintained satisfactorily. Further, since the second connection portion 10 of the medical connector 1 is closed by the valve body 11, the first connection portion 7 of the medical connector 1 is connected to the connected portion 6a of the first medical instrument 6. It is possible to maintain a state in which the connected portion 6a of the medical device 6 is closed by the medical connector 1.
 またこの状態において例えば誤操作により第2回転部材4が第1医療器具6に対して第2周方向C2に回転させられたとしても、回転伝達機構3は第2回転部材4を第1回転部材2に対して空回りさせる。したがって、第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。 Further, in this state, even if the second rotating member 4 is rotated in the second circumferential direction C2 with respect to the first medical instrument 6 due to, for example, an erroneous operation, the rotation transmission mechanism 3 makes the second rotating member 4 the first rotating member 2. Let it spin freely. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated from each other.
 またこの状態において、第2回転部材4の覆い部36は、第1回転部材2を把持できないように第1回転部材2を覆っている。したがって、第1回転部材2への誤操作により第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。 Further, in this state, the covering portion 36 of the second rotating member 4 covers the first rotating member 2 so that the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the first rotating member 2.
 またこの状態において、覆い部36は第1回転部材2の外側部分27を把持できないように第1回転部材2の外側部分27を覆っている。したがって、外側部分27への誤操作により第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。また、外側部分27の下端から覆い部36の下端までの第1軸方向A1の距離Dが-3mm以上である構成とした場合には、このような効果をより確実に得ることができる。 Further, in this state, the covering portion 36 covers the outer portion 27 of the first rotating member 2 so that the outer portion 27 of the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the outer portion 27. Further, when the distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is -3 mm or more, such an effect can be obtained more reliably.
 また、第1接続部7が第1医療器具6に接続された状態において覆い部36と第1医療器具6のロック筒6cとの間に軸方向Aに6mm以下の大きさの隙間Gが形成される構成とした場合には、隙間Gを通じて雌コネクタ部24を把持することはできない。したがって、第1接続部7の雌コネクタ部24への誤操作により第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。 Further, in a state where the first connecting portion 7 is connected to the first medical instrument 6, a gap G having a size of 6 mm or less is formed in the axial direction A between the covering portion 36 and the lock cylinder 6c of the first medical instrument 6. In this case, the female connector portion 24 cannot be gripped through the gap G. Therefore, it is possible to prevent the first connection portion 7 of the medical connector 1 from being separated from the connected portion 6a of the first medical device 6 due to an erroneous operation of the first connection portion 7 to the female connector portion 24.
 図6に示すように、第1接続部7が第1医療器具6に接続された状態から、必要に応じて第2医療器具9の被接続部9aを医療用コネクタ1の第2接続部10に接続することにより、第1医療器具6と第2医療器具9とを医療用コネクタ1を介して接続することができる。 As shown in FIG. 6, from the state where the first connecting portion 7 is connected to the first medical instrument 6, the connected portion 9a of the second medical instrument 9 is connected to the second connecting portion 10 of the medical connector 1 as needed. The first medical device 6 and the second medical device 9 can be connected to each other via the medical connector 1.
 この接続は、第2医療器具9の雄コネクタ部9bを医療用コネクタ1の第2接続部10の雌コネクタ部12に挿入し、この状態で第2医療器具9のロック筒9cを第1回転部材2に対して第1周方向C1に回転させることにより行われる。この接続は例えば、一方の手で第2回転部材4の覆い部36を把持する(図示省略)とともにもう一方の手で第2医療器具9のロック筒9cを把持し、ロック筒9cを覆い部36に対して第1周方向C1に回転させる操作によって行われる。 In this connection, the male connector portion 9b of the second medical instrument 9 is inserted into the female connector portion 12 of the second connection portion 10 of the medical connector 1, and in this state, the lock cylinder 9c of the second medical instrument 9 is rotated for the first time. This is done by rotating the member 2 in the first circumferential direction C1. In this connection, for example, one hand grips the covering portion 36 of the second rotating member 4 (not shown), and the other hand grips the lock cylinder 9c of the second medical device 9 to cover the lock cylinder 9c. It is performed by the operation of rotating the 36 in the first circumferential direction C1.
 このとき第1回転部材2の覆い部36を把持する代わりに、図6に示すように第1医療器具6のロック筒6cを把持した場合でも、第2接続部10がロック筒9cと共回りすることが回転伝達機構3によって規制されるので、ロック筒9cを第2接続部10に接続することができる。回転操作によって第2医療器具9の被接続部9aを第2接続部10に可逆的に接続することにより、第2接続部10での接続状態を良好に維持することができる。 At this time, instead of gripping the covering portion 36 of the first rotating member 2, even when the lock cylinder 6c of the first medical instrument 6 is gripped as shown in FIG. 6, the second connecting portion 10 rotates together with the lock cylinder 9c. Since this is restricted by the rotation transmission mechanism 3, the lock cylinder 9c can be connected to the second connection portion 10. By reversibly connecting the connected portion 9a of the second medical device 9 to the second connecting portion 10 by the rotation operation, the connected state at the second connecting portion 10 can be maintained satisfactorily.
 第2医療器具9のロック筒9cを医療用コネクタ1の第2接続部10から分離させるときには例えば、第2医療器具9のロック筒9cと第2回転部材4の覆い部36とをそれぞれ把持して回転させればよい。このとき第2回転部材4の覆い部36を把持する代わりに誤って第1医療器具6のロック筒6cを把持した場合でも、第1接続部7が第2医療器具9のロック筒9cと第2周方向C2に共回りすることが回転伝達機構3によって規制される。したがって、第1医療器具6のロック筒6cと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。 When the lock cylinder 9c of the second medical instrument 9 is separated from the second connection portion 10 of the medical connector 1, for example, the lock cylinder 9c of the second medical instrument 9 and the covering portion 36 of the second rotating member 4 are gripped, respectively. And rotate it. At this time, even if the lock cylinder 6c of the first medical device 6 is mistakenly gripped instead of gripping the cover portion 36 of the second rotating member 4, the first connecting portion 7 has the lock cylinder 9c and the third of the second medical device 9. Rotation transmission mechanism 3 regulates co-rotation in the two circumferential directions C2. Therefore, it is possible to prevent the lock cylinder 6c of the first medical device 6 and the first connection portion 7 of the medical connector 1 from being separated from each other.
 医療用コネクタ1は、第1医療器具6に一端接続した後は第1医療器具6の使用期間に亘って第1医療器具6から分離させることなく使用してもよいし、分離のための治具を設け、必要に応じて当該治具を用いて第1医療器具6から分離できるようにしてもよい。 The medical connector 1 may be used without being separated from the first medical device 6 for the period of use of the first medical device 6 after being once connected to the first medical device 6, or may be used for separation. A tool may be provided so that it can be separated from the first medical device 6 by using the jig if necessary.
 図7は、輸液ラインを形成するための輸液セット37の一例を示している。図7に示す輸液セット37は、図示しない輸液バッグ等の輸液保持具から、図示しない留置針までを接続する輸液ラインを形成するために用いられる。具体的には、輸液セット37は、第1医療用チューブとして構成された第1医療器具6と、医療用コネクタ1と、第2医療用チューブとして構成された第2医療器具9と、点滴筒38と、調整用クランプ39と、閉塞用クランプ40とを有している。点滴筒38は、輸液保持具から供給される輸液剤の流量を視認可能にする。調整用クランプ39は、輸液ライン内の輸液剤の流量を複数の状態へと変更可能である。閉塞用クランプ40は、輸液ラインを閉塞可能である。 FIG. 7 shows an example of an infusion set 37 for forming an infusion line. The infusion set 37 shown in FIG. 7 is used to form an infusion line connecting an infusion holder such as an infusion bag (not shown) to an indwelling needle (not shown). Specifically, the infusion set 37 includes a first medical device 6 configured as a first medical tube, a medical connector 1, a second medical device 9 configured as a second medical tube, and an intravenous drip tube. It has 38, an adjusting clamp 39, and a closing clamp 40. The drip tube 38 makes the flow rate of the infusion solution supplied from the infusion solution holder visible. The adjusting clamp 39 can change the flow rate of the infusion agent in the infusion line to a plurality of states. The occluding clamp 40 can occlude the infusion line.
 第1医療器具6の遠位端は、留置針の近位端に直接又は間接的に接続される。第1医療器具6の近位端には、医療用コネクタ1の第1接続部7に接続される被接続部6aが設けられている。第2医療器具9の遠位端には、医療用コネクタ1の第2接続部10に接続される被接続部9aが設けられている。第2医療器具9の近位端は、点滴筒38の遠位端に接続される。第2医療器具9の近位端は点滴筒38の遠位端に直接的に接続されているが、間接的に接続されてもよい。点滴筒38の近位端は輸液保持具に直接又は間接的に接続される。 The distal end of the first medical device 6 is directly or indirectly connected to the proximal end of the indwelling needle. At the proximal end of the first medical device 6, a connected portion 6a connected to the first connecting portion 7 of the medical connector 1 is provided. At the distal end of the second medical device 9, a connected portion 9a connected to the second connecting portion 10 of the medical connector 1 is provided. The proximal end of the second medical device 9 is connected to the distal end of the infusion tube 38. The proximal end of the second medical device 9 is directly connected to the distal end of the infusion tube 38, but may be indirectly connected. The proximal end of the drip tube 38 is directly or indirectly connected to the infusion holder.
 輸液セット37は、第1医療器具6、医療用コネクタ1、第2医療器具9、点滴筒38、調整用クランプ39及び閉塞用クランプ40を有する構成に限らず例えば、第1医療器具6、医療用コネクタ1及び第2医療器具9を有する構成であってもよい。 The infusion set 37 is not limited to the configuration having the first medical device 6, the medical connector 1, the second medical device 9, the drip tube 38, the adjusting clamp 39 and the closing clamp 40, for example, the first medical device 6, medical treatment. It may be configured to have a clamp 1 and a second medical device 9.
 第1実施形態では、第1医療器具6の被接続部6aが雄コネクタ部6bとロック筒6cとを有し、医療用コネクタ1の第1接続部7が雌コネクタ部24を有している。しかし、図8に示す第2実施形態の場合のように、第1医療器具6の被接続部6aが雌コネクタ部6dを有し、医療用コネクタ1の第1接続部7が雄コネクタ部41とロック筒42とを有してもよい。 In the first embodiment, the connected portion 6a of the first medical device 6 has a male connector portion 6b and a lock cylinder 6c, and the first connecting portion 7 of the medical connector 1 has a female connector portion 24. .. However, as in the case of the second embodiment shown in FIG. 8, the connected portion 6a of the first medical device 6 has the female connector portion 6d, and the first connecting portion 7 of the medical connector 1 has the male connector portion 41. And a lock cylinder 42 may be provided.
 図8に示す第2実施形態では、第1接続部7は、第1医療器具6の被接続部6aの雌コネクタ部6dに挿入される雄コネクタ部41と、雄コネクタ部41よりも径方向外側に位置するロック筒42とを有している。ロック筒42の内周面は、雌コネクタ部6dに対し第1周方向C1に回転することで凹凸形状同士の係合によって雌コネクタ部に可逆的に接続される係合部43を有している。 In the second embodiment shown in FIG. 8, the first connection portion 7 has the male connector portion 41 inserted into the female connector portion 6d of the connected portion 6a of the first medical device 6 and the male connector portion 41 in the radial direction with respect to the male connector portion 41. It has a lock cylinder 42 located on the outside. The inner peripheral surface of the lock cylinder 42 has an engaging portion 43 that is reversibly connected to the female connector portion by engaging the concave-convex shapes with each other by rotating in the first circumferential direction C1 with respect to the female connector portion 6d. There is.
 雌コネクタ部6dとロック筒42の係合部43との間における凹凸形状同士の係合は螺合であるが、これに限らない。第1接続部7は例えば、2016年のISO80369-7に準拠するように構成される。 The engagement between the concave-convex shapes between the female connector portion 6d and the engaging portion 43 of the lock cylinder 42 is screwed, but is not limited to this. The first connection unit 7 is configured to comply with, for example, ISO 80369-7 of 2016.
 第1回転部材2は、回転伝達機構3の一部を構成する外壁29とロック筒42とを備えるとともに雄コネクタ部41よりも径方向外側に位置する外側部分27を有している。覆い部36は、第1接続部7が第1医療器具6に接続された状態において、外側部分27を把持できないように外側部分27を覆うように構成されている。 The first rotating member 2 includes an outer wall 29 and a lock cylinder 42 that form a part of the rotation transmission mechanism 3, and also has an outer portion 27 that is located radially outside the male connector portion 41. The covering portion 36 is configured to cover the outer portion 27 so that the outer portion 27 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6.
 このように、覆い部36は、第1接続部7が第1医療器具6に接続された状態において第1回転部材2を把持できないように第1回転部材2を覆うように構成されている。外側部分27の下端から覆い部36の下端までの第1軸方向A1の距離Dは例えば、-3mm以上である。覆い部36は第2回転部材4のハウジング4aの一部で構成されている。より具体的に、覆い部36は外筒17で構成されているが、これに限らない。 As described above, the covering portion 36 is configured to cover the first rotating member 2 so that the first rotating member 2 cannot be gripped when the first connecting portion 7 is connected to the first medical device 6. The distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is, for example, -3 mm or more. The covering portion 36 is composed of a part of the housing 4a of the second rotating member 4. More specifically, the covering portion 36 is composed of an outer cylinder 17, but is not limited to this.
 第2実施形態に係る医療用コネクタ1は例えば、輸液セット37において第1実施形態の場合と同様に使用することができる。第2実施形態に係る医療用コネクタ1によれば、回転操作によって第1接続部7を第1医療器具6の被接続部6aに可逆的に接続することにより、第1接続部7での接続状態を良好に維持することができる。 The medical connector 1 according to the second embodiment can be used, for example, in the infusion set 37 in the same manner as in the case of the first embodiment. According to the medical connector 1 according to the second embodiment, the connection at the first connection portion 7 is made by reversibly connecting the first connection portion 7 to the connected portion 6a of the first medical instrument 6 by a rotation operation. The condition can be maintained in good condition.
 また第1接続部7が第1医療器具6に接続された状態において、第2回転部材4の覆い部36は、第1回転部材2を把持できないように第1回転部材2を覆っている。したがって、第1回転部材2への誤操作により第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。 Further, in a state where the first connecting portion 7 is connected to the first medical device 6, the covering portion 36 of the second rotating member 4 covers the first rotating member 2 so that the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the first rotating member 2.
 またこの状態において、覆い部36は第1回転部材2の外側部分27を把持できないように第1回転部材2の外側部分27を覆っている。したがって、外側部分27への誤操作により第1医療器具6の被接続部6aと医療用コネクタ1の第1接続部7との分離が生じることを抑制することができる。また、外側部分27の下端から覆い部36の下端までの第1軸方向A1の距離Dが-3mm以上である構成とした場合には、このような効果をより確実に得ることができる。 Further, in this state, the covering portion 36 covers the outer portion 27 of the first rotating member 2 so that the outer portion 27 of the first rotating member 2 cannot be gripped. Therefore, it is possible to prevent the connected portion 6a of the first medical device 6 and the first connecting portion 7 of the medical connector 1 from being separated due to an erroneous operation on the outer portion 27. Further, when the distance D in the first axial direction A1 from the lower end of the outer portion 27 to the lower end of the covering portion 36 is -3 mm or more, such an effect can be obtained more reliably.
 本開示に係る医療用コネクタは上記実施形態の構成に限らず、特許請求の範囲内で適宜変更可能である。 The medical connector according to the present disclosure is not limited to the configuration of the above embodiment, and can be appropriately changed within the scope of the claims.
 1  医療用コネクタ
 2  第1回転部材
 2a ハウジング
 3  回転伝達機構
 3a 回転連結部
 3b ラチェット機構
 4  第2回転部材
 4a ハウジング
 5  第1流路
 6  第1医療器具
 6a 被接続部
 6b 雄コネクタ部
 6c ロック筒
 6d 雌コネクタ部
 7  第1接続部
 8  第2流路
 9  第2医療器具
 9a 被接続部
 9b 雄コネクタ部
 9c ロック筒
10  第2接続部
11  弁体
11a スリット
11b 閉塞部
11c 固定部
12  第2接続部の雌コネクタ部
13  第2接続部の係合部
14  第2接続部の挿入口
15  内筒
16  フランジ
17  外筒
18  上キャップ
19  下キャップ
20  ホルダ
21  上部壁
22  貫通孔
23  中空部
24  第1接続部の雌コネクタ部
25  第1接続部の係合部
26  内側部分
27  外側部分
28  環状壁
29  外壁
30  密接部
31  係合部
32  環状溝
33  爪
34  凸部
35  変形部
36  覆い部
37  輸液セット
38  点滴筒
39  調整用クランプ
40  閉塞用クランプ
41  第1接続部の雄コネクタ部
42  第1接続部のロック筒
43  第1接続部の係合部
 A  軸方向
 A1 第1軸方向
 A2 第2軸方向
 C  周方向
 C1 第1周方向
 C2 第2周方向
 D  距離
 G  隙間
 O  軸線
1 Medical connector 2 1st rotating member 2a Housing 3 Rotating transmission mechanism 3a Rotating connecting part 3b Ratchet mechanism 4 2nd rotating member 4a Housing 5 1st flow path 6 1st medical equipment 6a Connected part 6b Male connector part 6c Lock cylinder 6d Female connector part 7 1st connection part 8 2nd flow path 9 2nd medical equipment 9a Connected part 9b Male connector part 9c Lock cylinder 10 2nd connection part 11 Valve body 11a Slit 11b Closure part 11c Fixation part 12 2nd connection Female connector part 13 Engagement part of the second connection part 14 Insertion part of the second connection part 15 Inner cylinder 16 Flange 17 Outer cylinder 18 Upper cap 19 Lower cap 20 Holder 21 Upper wall 22 Through hole 23 Hollow part 24 First Female connector part of the connection part 25 Engagement part of the first connection part 26 Inner part 27 Outer part 28 Circular wall 29 Outer wall 30 Close contact part 31 Engagement part 32 Ring groove 33 Claw 34 Convex part 35 Deformation part 36 Cover part 37 Infusion set 38 Drip tube 39 Adjustment clamp 40 Closure clamp 41 Male connector part of the first connection part 42 Lock cylinder part of the first connection part 43 Engagement part of the first connection part A Axial direction A1 1st axial direction A2 2nd axial direction C Circumferential direction C1 1st circumferential direction C2 2nd circumferential direction D Distance G Gap O Axis line

Claims (11)

  1.  第1回転部材と、前記第1回転部材に回転伝達機構を介して連結される第2回転部材とを有し、
     前記第1回転部材は、第1流路を区画するとともに第1医療器具に対し軸線を中心として第1周方向に回転することで前記第1医療器具に可逆的に接続される第1接続部を有し、
     前記第2回転部材は、前記第1流路と連通する第2流路を区画するとともに前記第2医療器具に可逆的に接続される第2接続部を有し、
     前記回転伝達機構は、前記第2回転部材が前記第1回転部材に対して前記第1周方向に回転することを規制する一方、前記第2回転部材が前記第1回転部材に対して前記第1周方向の反対方向である第2周方向に回転することを許容し、
     前記第2回転部材は、前記第1接続部が前記第1医療器具に接続された状態において前記第1回転部材を把持できないように前記第1回転部材を覆う覆い部を有する医療用コネクタ。
    It has a first rotating member and a second rotating member connected to the first rotating member via a rotation transmission mechanism.
    The first rotating member is a first connecting portion that is reversibly connected to the first medical device by partitioning the first flow path and rotating in the first circumferential direction about an axis with respect to the first medical device. Have,
    The second rotating member has a second connecting portion that partitions the second flow path communicating with the first flow path and is reversibly connected to the second medical device.
    The rotation transmission mechanism restricts the second rotating member from rotating in the first circumferential direction with respect to the first rotating member, while the second rotating member has the first rotation with respect to the first rotating member. Allows rotation in the second lap direction, which is the opposite direction of the first lap direction,
    The second rotating member is a medical connector having a covering portion that covers the first rotating member so that the first rotating member cannot be gripped in a state where the first connecting portion is connected to the first medical device.
  2.  前記第1医療器具は、雄コネクタ部と前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、
     前記第1接続部は、前記雄コネクタ部を挿入される雌コネクタ部を有し、
     前記雌コネクタ部の外周面は、前記ロック筒に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記ロック筒に可逆的に接続される係合部を有する、請求項1に記載の医療用コネクタ。
    The first medical device has a male connector portion and a lock cylinder located radially outside the male connector portion.
    The first connection portion has a female connector portion into which the male connector portion is inserted.
    1. The outer peripheral surface of the female connector portion has an engaging portion that is reversibly connected to the lock cylinder by engaging the concave-convex shapes with each other by rotating in the first circumferential direction with respect to the lock cylinder. Medical connector described in.
  3.  前記第1回転部材は、前記回転伝達機構の一部を構成する外壁を備えるとともに前記雌コネクタ部よりも径方向外側に位置する外側部分を有し、
     前記覆い部は、前記第1接続部が前記第1医療器具に接続された状態において、前記外側部分を把持できないように前記外側部分を覆う、請求項2に記載の医療用コネクタ。
    The first rotating member includes an outer wall forming a part of the rotation transmission mechanism and has an outer portion located radially outside the female connector portion.
    The medical connector according to claim 2, wherein the covering portion covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
  4.  前記第1接続部が前記第1医療器具に接続された状態において、前記覆い部と前記ロック筒との間に前記軸線に沿う方向に6mm以下の大きさの隙間が形成される、請求項3に記載の医療用コネクタ。 3. The third aspect of the present invention, in which the first connecting portion is connected to the first medical device, and a gap having a size of 6 mm or less is formed between the covering portion and the lock cylinder in a direction along the axis. Medical connector described in.
  5.  前記第1医療器具は雌コネクタ部を有し、
     前記第1接続部は、前記雌コネクタ部に挿入される雄コネクタ部と、前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、
     前記ロック筒の内周面は、前記雌コネクタ部に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記雌コネクタ部に可逆的に接続される係合部を有する、請求項1に記載の医療用コネクタ。
    The first medical device has a female connector portion and has a female connector portion.
    The first connection portion has a male connector portion inserted into the female connector portion and a lock cylinder located radially outside the male connector portion.
    The inner peripheral surface of the lock cylinder has an engaging portion that is reversibly connected to the female connector portion by engaging the concave-convex shapes with each other by rotating in the first circumferential direction with respect to the female connector portion. Item 1. The medical connector according to item 1.
  6.  前記第1回転部材は、前記回転伝達機構の一部を構成する外壁と前記ロック筒とを備えるとともに前記雄コネクタ部よりも径方向外側に位置する外側部分を有し、
     前記覆い部は、前記第1接続部が前記第1医療器具に接続された状態において、前記外側部分を把持できないように前記外側部分を覆う、請求項5に記載の医療用コネクタ。
    The first rotating member includes an outer wall forming a part of the rotation transmission mechanism and the lock cylinder, and has an outer portion located radially outside the male connector portion.
    The medical connector according to claim 5, wherein the covering portion covers the outer portion so that the outer portion cannot be gripped in a state where the first connecting portion is connected to the first medical device.
  7.  前記第2医療器具は、前記第2接続部に対し前記軸線を中心として回転することで前記第2接続部に可逆的に接続される、請求項1~6の何れか1項に記載の医療用コネクタ。 The medical device according to any one of claims 1 to 6, wherein the second medical device is reversibly connected to the second connection portion by rotating about the axis with respect to the second connection portion. Connector for.
  8.  前記第2医療器具は、前記第2接続部に対し前記第1周方向に回転することで前記第2接続部に可逆的に接続される、請求項1~7の何れか1項に記載の医療用コネクタ。 The second medical device according to any one of claims 1 to 7, wherein the second medical device is reversibly connected to the second connection portion by rotating in the first circumferential direction with respect to the second connection portion. Medical connector.
  9.  前記第2接続部は前記第2流路を閉塞する弁体を有する、請求項1~8の何れか1項に記載の医療用コネクタ。 The medical connector according to any one of claims 1 to 8, wherein the second connection portion has a valve body that closes the second flow path.
  10.  前記第2医療器具は雄コネクタ部を有し、
     前記第2接続部は、前記雄コネクタ部を挿入される挿入口を備える雌コネクタ部を有し、
     前記弁体は、前記挿入口を閉塞するとともにスリットを備える円板状の閉塞部と、前記閉塞部の外周縁に連なるとともに前記挿入口に固定される固定部とを有する弾性弁体であり、
     前記スリットは、前記雄コネクタ部が前記閉塞部を前記挿入口から前記第2流路内に押し込むことにより開口する、請求項9に記載の医療用コネクタ。
    The second medical device has a male connector portion and has a male connector portion.
    The second connection portion has a female connector portion having an insertion port into which the male connector portion is inserted.
    The valve body is an elastic valve body having a disk-shaped closing portion that closes the insertion port and has a slit, and a fixing portion that is connected to the outer peripheral edge of the closing portion and is fixed to the insertion port.
    The medical connector according to claim 9, wherein the slit is opened by the male connector portion pushing the closed portion into the second flow path from the insertion port.
  11.  前記第2医療器具は、雄コネクタ部と前記雄コネクタ部よりも径方向外側に位置するロック筒とを有し、
     前記第2接続部は、前記雄コネクタ部を挿入される雌コネクタ部を有し、
     前記雌コネクタ部の外周面は、前記ロック筒が前記雌コネクタ部に対し前記第1周方向に回転することで凹凸形状同士の係合によって前記ロック筒に可逆的に接続される係合部を有する、請求項1~10の何れか1項に記載の医療用コネクタ。
    The second medical device has a male connector portion and a lock cylinder located radially outside the male connector portion.
    The second connection portion has a female connector portion into which the male connector portion is inserted.
    The outer peripheral surface of the female connector portion is an engaging portion that is reversibly connected to the lock cylinder by engaging the concave-convex shapes with each other by rotating the lock cylinder with respect to the female connector portion in the first circumferential direction. The medical connector according to any one of claims 1 to 10.
PCT/JP2020/041765 2019-12-20 2020-11-09 Medical connector WO2021124727A1 (en)

Applications Claiming Priority (2)

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JP2019-230732 2019-12-20
JP2019230732 2019-12-20

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2712652A2 (en) * 2012-09-28 2014-04-02 Vygon Anti-unscrewing medical connection system
US20170036008A1 (en) * 2015-08-06 2017-02-09 Hsi-Chin Tsai Closed male luer
WO2019130891A1 (en) * 2017-12-26 2019-07-04 テルモ株式会社 Medical connector

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2712652A2 (en) * 2012-09-28 2014-04-02 Vygon Anti-unscrewing medical connection system
US20170036008A1 (en) * 2015-08-06 2017-02-09 Hsi-Chin Tsai Closed male luer
WO2019130891A1 (en) * 2017-12-26 2019-07-04 テルモ株式会社 Medical connector

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