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NL2030451A - Blood pump for percutaneous insertion into patient blood vessel - Google Patents

Blood pump for percutaneous insertion into patient blood vessel Download PDF

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Publication number
NL2030451A
NL2030451A NL2030451A NL2030451A NL2030451A NL 2030451 A NL2030451 A NL 2030451A NL 2030451 A NL2030451 A NL 2030451A NL 2030451 A NL2030451 A NL 2030451A NL 2030451 A NL2030451 A NL 2030451A
Authority
NL
Netherlands
Prior art keywords
blood
catheter
tube
flexible cannula
patient
Prior art date
Application number
NL2030451A
Other languages
Dutch (nl)
Other versions
NL2030451B1 (en
Inventor
Feng Qitao
Gong Zheng
Xie Qilian
Liu Huan
Original Assignee
Anhui Tongling Bionic Tech Co Ltd
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 Anhui Tongling Bionic Tech Co Ltd filed Critical Anhui Tongling Bionic Tech Co Ltd
Publication of NL2030451A publication Critical patent/NL2030451A/en
Application granted granted Critical
Publication of NL2030451B1 publication Critical patent/NL2030451B1/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
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/10Location thereof with respect to the patient's body
    • A61M60/122Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body
    • A61M60/126Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel
    • A61M60/13Implantable pumps or pumping devices, i.e. the blood being pumped inside the patient's body implantable via, into, inside, in line, branching on, or around a blood vessel by means of a catheter allowing explantation, e.g. catheter pumps temporarily introduced via the vascular system
    • 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/0009Making of catheters or other medical or surgical tubes
    • A61M25/0012Making of catheters or other medical or surgical tubes with embedded structures, e.g. coils, braids, meshes, strands or radiopaque coils
    • 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/0043Catheters; Hollow probes characterised by structural features
    • A61M25/005Catheters; Hollow probes characterised by structural features with embedded materials for reinforcement, e.g. wires, coils, braids
    • 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
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/20Type thereof
    • A61M60/205Non-positive displacement blood pumps
    • A61M60/216Non-positive displacement blood pumps including a rotating member acting on the blood, e.g. impeller
    • A61M60/237Non-positive displacement blood pumps including a rotating member acting on the blood, e.g. impeller the blood flow through the rotating member having mainly axial components, e.g. axial flow pumps
    • 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
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/40Details relating to driving
    • A61M60/403Details relating to driving for non-positive displacement blood pumps
    • A61M60/408Details relating to driving for non-positive displacement blood pumps the force acting on the blood contacting member being mechanical, e.g. transmitted by a shaft or cable
    • A61M60/411Details relating to driving for non-positive displacement blood pumps the force acting on the blood contacting member being mechanical, e.g. transmitted by a shaft or cable generated by an electromotor
    • A61M60/416Details relating to driving for non-positive displacement blood pumps the force acting on the blood contacting member being mechanical, e.g. transmitted by a shaft or cable generated by an electromotor transmitted directly by the motor rotor drive shaft
    • 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
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/80Constructional details other than related to driving
    • A61M60/802Constructional details other than related to driving of non-positive displacement blood pumps
    • A61M60/827Sealings between moving parts
    • A61M60/829Sealings between moving parts having a purge fluid supply
    • 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
    • A61M60/00Blood pumps; Devices for mechanical circulatory actuation; Balloon pumps for circulatory assistance
    • A61M60/80Constructional details other than related to driving
    • A61M60/855Constructional details other than related to driving of implantable pumps or pumping devices
    • A61M60/871Energy supply devices; Converters therefor

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Mechanical Engineering (AREA)
  • Cardiology (AREA)
  • Biophysics (AREA)
  • Pulmonology (AREA)
  • Vascular Medicine (AREA)
  • External Artificial Organs (AREA)

Abstract

UITTREKSEL The utility model relates to the field of medical device technique and discloses a blood, pump for percutaneous insertion into a patient's blood vessel, comprising a catheter and a pumping installation attached, to the said catheter, the said catheter 5 extending along the longitudinal axis and having a lumen in which an electrical wire and a cleaning tube are provided extending from the proximal to the distal end, the cleaning tube being constructed to receive the pressurized fluid, and the said lumen having a flexible cannula in which the electrical wire and/or 10 cleaning tube is provided. The flexible cannula is used to accommodate the electrical wire, optical fiber and cleaning tube, and then it is placed in the catheter, thus improving the overall flexural properties of the catheter, facilitating resistance to radial deformation and providing structural support for the smooth l5 operation of the catheter in the blood vessel.

Description

BLOOD PUMP FOR PERCUTANEOUS INSERTION INTO PATIENT BLOOD VESSEL
TECHNICAL FIELD The utility model relates to the field of medical device technique, in particular to a blood pump for percutaneous inser- tion into a patient's blood vessel.
BACKGROUND ART Blood pumps, also known as mechanical blood circulation sup- port device or ventricular assist device, can be introduced percu- taneously into the heart and can be so constructed that it assists or replaces the natural cardiac pumping function by circulatory or continuous pumping of blood to provide hemodynamic support for cardiogenic shock and acute heart failure.
The prior art is the technical scheme adopted by the patent with a Chinese Patent Publication No. of CN202022033733.9, which include a pigtail tube, a blood inflow port, a blood flow channel, a blood outflow port, a motor and an extension tube which are con- nected and fixed in turn, with the said pigtail tube, blood inflow port, blood flow channel, blood outflow port, motor and extension tube covered with polyurethane film on the outer side, and a blood inlet and a blood outlet provided at the polyurethane films corre- sponding to the blood inflow port and the blood outflow port re- spectively. The surface of the heart assist device is covered with a polyurethane film that extends from the pigtail tube to the ex- tension tube and is hollowed out at the positions corresponding to the blood inflow port and blood outflow port to form the blood in- let and blood outlet, so that the risk of component fall off is completely eliminated and the safety of using this heart assist device is greatly increased.
The motor is located inside the motor housing, with a clear- ance formed between the motor's rotating shaft and the motor hous- ing. Blood can enter the motor housing through the clearance and bring about adverse effects such as thrombosis and hemolysis. A cleaning tube is so set that it extends from the outside into the motor housing through the catheter, and the cleaning fluid, such as heparin, can push out the blood at the clearance by flowing in the motor housing so as to prevent the blood from entering the housing. However, due to the tortuous path of the blood vessels, radial deformation, such as bending, may occur in the extension tube during the process of pushing the blood pump into the heart, resulting in obstruction of the flow of cleaning fluid in the cleaning tube and adversely affecting the function of the blood pump.
SUMMARY In response to the problems in the prior art, the utility model aims to provide a blood pump for percutaneous insertion into a patient's blood vessel.
The technical problem to be solved by the utility model is solved using the following technical scheme: a blood pump for per- cutaneous insertion into a patient's blood vessel, comprising a catheter and a pumping installation attached to the said catheter, the said catheter extending along the longitudinal axis and having a lumen in which an electrical wire and a cleaning tube are pro- vided extending from the proximal to the distal end, the cleaning tube being constructed to receive the pressurized fluid, and the said lumen having a flexible cannula in which the electrical wire and/or cleaning tube is provided.
Preferably, the said flexible cannula is of spiral structure or porous three-dimensional structure.
Preferably, the said flexible cannula is a spiral coil or a rubber tube or a braided tube or a hollowed-out tube. Preferably, the said flexible cannula comprises a shape memory material, preferably a shape memory alloy, and more prefer- ably Nitinol.
Preferably, the said braided tube is made of knitted fabric, knotted fabric, woven fabric or non-woven fabric. Preferably, the said flexible cannula extends intermittently or continuously in the lumen.
Preferably, the said flexible cannula has an external dimen- sion suitable for the catheter passing through and an internal di-
mension capable of accommodating the electrical wire and/or clean- ing tube.
The beneficial effects of the utility model are as follows: In the utility model, the flexible cannula is used to accom- modate the electrical wire and cleaning tube, and then it is placed in the extension tube, thus improving the overall flexural properties of the extension tube, facilitating resistance to radi- al deformation and providing structural support for the smooth op- eration of the extension tube in the blood vessel.
BRIEF DESCRIPTION OF THE DRAWINGS In order to more clearly illustrate the technical scheme in the utility model embodiments, the following is a brief descrip- tion of the attached figures to be used in the description of the embodiments. It is obvious that the following attached figures in the description are only some embodiments of the utility model and, for a person with ordinary skill in the field, other attached figures can be obtained according to these attached figures with- out creative work.
Figure 1 is a structural diagram of a blood pump for percuta- neous insertion into a patient's blood vessel in the utility mod- el; Figure 2 is a schematic diagram for the internal structure of the motor housing in the utility model.
Figure 3 is a partial enlarged drawing of Part A in Figure 2 of the utility model.
Figure 4 is a structural schematic diagram for the longitudi- nal section of the extension tube in the utility model. Figure 5 is a partial enlarged drawing of Part B in Figure 4 of the utility model.
Figure 6 is a structural schematic diagram for the cross sec- tion of the flexible cannula in the utility model.
In the figures: 101. catheter; 102. motor housing; 103. blood outflow port; 104. blood flow channel; 105. blood inflow port;
106. pigtail tube; 201. flexible cannula; 202. cleaning tube; 203. electric wire; 301. motor; 302. axial impeller.
DETAILED DESCRIPTION OF THE EMBODIMENTS In order to make the technical means, creative features, pur- pose and efficacy of the utility model is easy to understand, the utility model is further elaborated in combination with the spe- cific figures.
Embodiment 1 As shown in Figure 1, in the prior art, the complete blood pump suitable for left ventricular assistance includes a pigtail tube 106, a blood inflow port 105, a blood flow channel 104, a blood outflow port 103, a motor housing 102 and an extension tube 101 connected and fixed in turn, a motor 301 mounted inside the motor housing 102, the rotating shaft of the motor 301 running through the motor 301 housing and fixedly connected to the axial impeller 302 connected in a rotatable manner inside the blood flow channel 104, and the electric wire 204, optical fiber 203 and cleaning tube 202 arranged inside the extension tube 101. When the blood pump is in use, the blood flow channel 104 can extend and pass the aortic valve so that the blood inflow port 105 and pigtail tube 106 cross the aortic valve and are positioned in the left ventricle; the motor 301 drives the axial impeller 302 to rotate and, under this driving effect, the blood in the left ven- tricle is pumped into the pump at the blood inflow port 105 and flows out of the pump via the blood outflow port 103 and flows in- to the aorta; radial deformation, such as bending, may occur in the extension tube during the process of pushing the blood pump into the heart, resulting in obstruction of the flow of cleaning fluid in the cleaning tube and adversely affecting the function of the blood pump.
Embodiment 2 As shown in Figures 1-6, a blood pump for percutaneous inser- tion into a patient's blood vessel comprises a catheter 101 and a pumping installation attached to the said catheter 101, the said catheter 101 extending along the longitudinal axis and having a lumen in which an electrical wire 204 and a cleaning tube 202 are provided extending from the proximal to the distal end, and the cleaning tube 202 being constructed to receive the pressurized fluid, inside the said lumen a flexible cannula 201 set, and the electrical wire 204 and/or cleaning tube 202 set in the flexible cannula 201.
The said flexible cannula 201 is of spiral structure or po- rous three-dimensional structure.
5 The said flexible cannula 201 is a spiral coil or a rubber tube or a braided tube or a hollowed-out tube.
The said flexible cannula 201 comprises a shape memory mate- rial, preferably a shape memory alloy, and more preferably Nitin- ol.
The said braided tube is made of knitted fabric, knotted fab- ric, woven fabric or non-woven fabric.
The said flexible cannula 201 extends intermittently or con- tinuously in the lumen.
The said flexible cannula 201 has an external dimension suit- able for the catheter passing through and an internal dimension capable of accommodating the electrical wire 204 and/or cleaning tube 202.
The flexible cannula 201 is used to accommodate the electri- cal wire 203 and cleaning tube 202, and then it is placed in the catheter 101, thus improving the overall flexural properties of the catheter 101, facilitating resistance to radial deformation and providing structural support for the smooth operation of the catheter 101 in the blood vessel.
It is important to note that in this document, terms such as first and second are used only to distinguish one entity or opera- tion from another and do not necessarily require or imply any ac- tual relationship or order between these entities or operations. Further, the terms "include", "comprise" or any other variation thereof are intended to cover non-exclusive inclusion such that a process, method, article, or apparatus comprising a set of ele- ments includes not only those elements, but also other elements not expressly listed, or elements inherent to such process, meth- od, article, or apparatus. Without further limitation, the ele- ments defined by the statement "including a ......" do not pre- clude the existence of additional identical elements in such pro- cess, method, article or apparatus as includes the said elements.
The above shows and describes the basic philosophy, main characteristics and advantages of the utility model.
A person skilled in the art should understand that the utility model is not limited by the above embodiments.
The above embodiments and those described in the specification only illustrate the philosophy of the utility model, and there will be various changes and improve- ments to the utility model without departing from the spirit and scope of the utility model, and these changes and improvements all fall within the scope of the utility model for which protection is requested.
The utility model claims a scope of protection defined by the appended claims and their equivalents.

Claims (7)

CONCLUSIESCONCLUSIONS 1. Bloedpomp voor percutane inbrenging in het bloedvat van een pa- tiënt, omvattende een katheter en een pompinstallatie die aan de katheter is bevestigd, waarbij de katheter zich uitstrekt langs de lengteas en een lumen heeft waarin een elektrische draad en een reinigingsbuis zijn aangebracht die zich uitstrekken van het proximale uiteinde naar het distale uiteinde, en waarbij de reini- gingsbuis is geconstrueerd om de onder druk gebrachte vloeistof te ontvangen, met het kenmerk, dat binnen het genoemde lumen een flexibele canule is geplaatst en de elektrische draad en/of reini- gingsbuis is geplaatst in de flexibele canule.A blood pump for percutaneous insertion into a patient's blood vessel, comprising a catheter and a pumping device attached to the catheter, the catheter extending along its longitudinal axis and having a lumen in which there are disposed an electrical wire and a cleaning tube that extending from the proximal end to the distal end, and wherein the cleaning tube is constructed to receive the pressurized fluid, characterized in that a flexible cannula is placed within said lumen and the electrical wire and/or cleaning agent - Ging tube is placed in the flexible cannula. 2. Bloedpomp voor percutane inbrenging in een bloedvat van een pa- tiënt, volgens conclusie 1, met het kenmerk, dat de flexibele ca- nule een spiraalstructuur of een poreuze driedimensionale struc- tuur heeft.The blood pump for percutaneous insertion into a blood vessel of a patient, according to claim 1, characterized in that the flexible cannula has a spiral structure or a porous three-dimensional structure. 3. Bloedpomp voor percutane inbrenging in een bloedvat van een pa- tiënt, zoals beschreven in conclusie 1 of 2, met het kenmerk, dat de flexibele canule een geschroefde spiraal of een rubberen slang of een gevlochten slang of een uitgeholde slang is.A blood pump for percutaneous insertion into a blood vessel of a patient as described in claim 1 or 2, characterized in that the flexible cannula is a threaded coil or a rubber tube or a braided tube or a hollowed-out tube. 4. Bloedpomp voor percutane inbrenging in het bloedvat van een pa- tiënt, zoals beschreven in een van de conclusies 1-3, welke wordt gekenmerkt doordat de genoemde flexibele canule een vormgeheugen- materiaal omvat, bij voorkeur een vormgeheugenlegering, en met meer voorkeur Nitinol.A blood pump for percutaneous insertion into a patient's blood vessel as described in any one of claims 1 to 3, characterized in that said flexible cannula comprises a shape memory material, preferably a shape memory alloy, and more preferably Nitinol . 5. Bloedpomp voor percutane inbrenging in een bloedvat van een pa- tiënt, zoals beschreven in conclusie 3, met het kenmerk, dat de gevlochten buis is gemaakt van breiwerk, knoopstof, geweven stof of niet-geweven stof.A blood pump for percutaneous insertion into a blood vessel of a patient as described in claim 3, characterized in that the braided tube is made of knitted fabric, button fabric, woven fabric or non-woven fabric. 6. Bloedpomp voor percutane inbrenging in een bloedvat van een pa- tiënt, zoals beschreven in een van de conclusies 1 tot en met 5,A blood pump for percutaneous insertion into a blood vessel of a patient, as described in any one of claims 1 to 5, met het kenmerk, dat de gencemde flexibele canule zich intermitte- rend of continu in het lumen uitstrekt.characterized in that the cemented flexible cannula extends intermittently or continuously into the lumen. 7. Bloedpomp voor percutane inbrenging in een bloedvat van een pa- tiënt, zoals beschreven in een van de conclusies 1 tot en met 6, met het kenmerk, dat de flexibele canule een uitwendige afmeting heeft die geschikt is voor het daar doorheen voeren van de kathe- ter en een inwendige afmeting heeft die geschikt is voor het opne- men van de elektrische draad en/of reinigingsbuis.A blood pump for percutaneous insertion into a blood vessel of a patient as set forth in any one of claims 1 to 6, characterized in that the flexible cannula has an outer dimension suitable for passing the said flexible cannula therethrough. catheter and has an internal size suitable for receiving the electrical wire and/or cleaning tube.
NL2030451A 2021-11-15 2022-01-06 Blood pump for percutaneous insertion into patient blood vessel NL2030451B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202122783525.5U CN218485008U (en) 2021-11-15 2021-11-15 Blood pump for percutaneous insertion into blood vessel of patient

Publications (2)

Publication Number Publication Date
NL2030451A true NL2030451A (en) 2022-05-16
NL2030451B1 NL2030451B1 (en) 2024-11-25

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Family Applications (1)

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NL2030451A NL2030451B1 (en) 2021-11-15 2022-01-06 Blood pump for percutaneous insertion into patient blood vessel

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NL (1) NL2030451B1 (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030176835A1 (en) * 2002-03-15 2003-09-18 Sun Medical Technology Research Corporation Protector and blood pump system
AU2013254644A1 (en) * 2012-04-27 2014-11-13 Abiomed Europe Gmbh Catheter system and intravascular blood pump comprising said catheter system
US20180064862A1 (en) * 2013-03-13 2018-03-08 Tc1 Llc Sheath assembly for catheter pump
WO2018202775A1 (en) * 2017-05-04 2018-11-08 Abiomed Europe Gmbh Blood pump with reinforced catheter
WO2020018742A1 (en) * 2018-07-19 2020-01-23 Abiomed, Inc. Systems and methods for reducing leaks from a catheter
WO2020120342A1 (en) * 2018-12-11 2020-06-18 Abiomed Europe Gmbh Catheter for intravascular blood pump
WO2020152611A2 (en) * 2019-01-24 2020-07-30 Magenta Medical Ltd Ventricular assist device

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030176835A1 (en) * 2002-03-15 2003-09-18 Sun Medical Technology Research Corporation Protector and blood pump system
AU2013254644A1 (en) * 2012-04-27 2014-11-13 Abiomed Europe Gmbh Catheter system and intravascular blood pump comprising said catheter system
US20180064862A1 (en) * 2013-03-13 2018-03-08 Tc1 Llc Sheath assembly for catheter pump
WO2018202775A1 (en) * 2017-05-04 2018-11-08 Abiomed Europe Gmbh Blood pump with reinforced catheter
WO2020018742A1 (en) * 2018-07-19 2020-01-23 Abiomed, Inc. Systems and methods for reducing leaks from a catheter
WO2020120342A1 (en) * 2018-12-11 2020-06-18 Abiomed Europe Gmbh Catheter for intravascular blood pump
WO2020152611A2 (en) * 2019-01-24 2020-07-30 Magenta Medical Ltd Ventricular assist device

Also Published As

Publication number Publication date
CN218485008U (en) 2023-02-17
NL2030451B1 (en) 2024-11-25

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