Foaming test bag

Abstract

The utility model discloses a foaming test bag which comprises a foaming test bag body, and a disinfection bag placing position, a fixing band placing position, a combined three-way device placing position, a fixing film placing position, a 10ml pre-filled normal saline placing position, a 9ml pre-filled normal saline placing position and a spiral connector 10ml injector placing position are arranged in the foaming test bag body. The top of the foaming experiment bag body is provided with a disinfection bag placing position and a fixing band placing position, the middle part of the foaming experiment bag body is provided with a combined three-way device placing position and a fixing film placing position, and the tail part of the foaming experiment bag body is provided with a 10ml pre-filled normal saline placing position, a 9ml pre-filled normal saline placing position and a spiral interface 10ml injector placing position. The three-way device is provided with the locking assembly, so that an injector can be effectively fixed and is prevented from falling off, all instruments for a foaming experiment are directly prepared through the foaming experiment bag body, and the time for medical staff to prepare the instruments is greatly shortened.

Description

TECHNICAL FIELD

[0001] The utility model belongs to the field of medical supplies, especially relates to a foaming test bag. BACKGROUND

[0002] Clinical foaming experiment, full name is transcranial doppler ultrasound foaming experiment, is a kind of through transcranial doppler ultrasound technology, monitoring cerebral vascular microembolus (air embolus) quantity inspection method;Foaming test is mainly used for diagnosing patent foramen ovale, it is a kind of common congenital heart disease.Patent foramen ovale can cause venous system embolus to avoid lung circulation directly to reach brain tissue through open patent foramen ovale, to cause migraine, cerebral infarction, syncope and a series of clinical syndromes.

[0003] At present, there is no special experimental bag for transcranial doppler ultrasound foaming experiment in clinic, and the foaming experiment supplies are more and more miscellaneous, so it is troublesome for medical staff to find them, and it is difficult to centrally place the foaming experiment equipment, and medical staff needs to spend a lot of time to prepare medical supplies every time, and since each medical supply is placed in different places, it not only wastes time, but also reduces medical efficiency.

[0004] At present, the foaming experiment is activated by using three-way pipe and two injectors to foam physiological saline, and the injector and the three-way pipe are easy to separate in the foaming process. UTILITY MODEL CONTENT

[0005] The utility model aims at providing a kind of foaming test bag, to solve the problems in the background art.To achieve the purpose, the technical scheme adopted by the utility model is:

[0006] The utility model provides a kind of foaming test package, including foaming experimental package body, the inside of foaming experimental package body is provided with sterilization package place, fixed band place, joint three-way device place, fixed film place, 10ml pre-filled physiological saline place, 9ml pre-filled physiological saline place and screw interface 10ml syringe place, the top of foaming experimental package body is provided with sterilization package place and fixed band place, sterilization package place is built-in iodophor cotton swab package, fixed band place is built-in velcro fixed band, the middle part of foaming experimental package body is provided with joint three-way device place and fixed film place, joint three-way device place is built-in joint three-way device, fixed film place is built-in puncture fixed dressing 1, the tail of foaming experimental package body is provided with 10ml pre-filled physiological saline place, 9ml pre-filled physiological saline place and screw interface 10ml syringe place, 10ml pre-filled physiological saline place is built-in 3 10ml pre-filled physiological saline injectors, 9ml pre-filled physiological saline place is built-in 3 10ml pre-filled 9ml physiological saline injectors, screw interface 10ml syringe place is built-in 3 10ml injectors.

[0007] Preferably, the three-way device includes a main pipe, a first three-way valve, a second three-way valve, a first connector, a second connector, a third connector, a fourth connector, a first locking assembly, a second locking assembly, and a third locking assembly. The two ends of the main pipe are integrally formed with the first three-way valve and the second three-way valve, respectively. The first three-way valve is provided with the first connector and the second connector, which are used to connect the syringe. The first connector and the second connector are respectively connected with the first locking assembly and the second locking assembly, which are used to lock the syringe. The second three-way valve is provided with the third connector and the fourth connector. The third connector is used to connect the syringe, and is connected with the third locking assembly, which is used to lock the syringe. The fourth connector is used to threadedly connect the intravenous indwelling needle or the stop valve.

[0008] Preferably, the inside of the foaming experimental package body is placed with a tourniquet.

[0009] Preferably, the inside of the foaming experimental package body is also placed with a straight trocar.

[0010] Preferably, the velcro fixed band is 1CM.

[0011] Preferably, the syringes are screw-threaded syringes, which are matched with the interfaces of the three-way device.

[0012] The utility model has the advantages that: all the materials for foaming experiment are prepared directly in the foaming experimental package body, which greatly reduces the time for medical staff to prepare materials and improves the medical efficiency. The multiple placement areas make the materials placed reasonably and easily distinguished during the foaming experiment, which is convenient to use. BRIEF DESCRIPTION OF DRAWINGS

[0013]

[0013] Fig. 1 The overall schematic view is provided for the embodiment of the utility model;

[0014] Fig. 2 The three-way device structure schematic view is provided for the embodiment of the utility model;

[0015] In the drawing, various reference signs are:

[0016] 1, foaming experiment package body;2, disinfection package placement;21, iodophor cotton swab package;3, fixed band placement;31, velcro fixed band;4, joint three-way device placement;41, three-way device;4101, main pipeline;4102, first three-way valve;4103, second three-way valve;4104, first joint;4105, second joint;4106, third joint;4107, fourth joint;4108, first locking assembly;4109, second locking assembly;4110, third locking assembly;5, fixed film placement;51, puncture fixed dressing;6, 10ml pre-filled normal saline placement;61, 10ml pre-filled normal saline syringe;7, 9ml pre-filled normal saline placement;71, 10ml pre-filled 9ml normal saline syringe;8, spiral interface 10ml syringe placement;81, 10ml syringe;9, tourniquet;10, straight cannula needle. DETAILED DESCRIPTION

[0017] In order to facilitate the understanding of the utility model, the utility model will be described more fully below with reference to the relevant drawings. The preferred embodiments of the utility model are shown in the drawings. However, the utility model can be realized in many different forms and is not limited to the embodiments described herein. On the contrary, the purpose of providing these embodiments is to make the disclosure of the utility model more thorough and comprehensive.

[0018] It should be noted that when an element is referred to as being "fixed to" another element, it can be directly on the other element or there can be an intervening element. When an element is referred to as being "connected to" another element, it can be directly connected to the other element or there can be an intervening element. Conversely, when an element is referred to as being "directly on" another element, there is no intervening element. The terms "vertical", "horizontal", "left", "right" and similar expressions used herein are for illustrative purposes only and are not intended to be the only embodiment. The terms "upper end", "lower end", "left side", "right side", "front end", "rear end" and similar expressions used herein are with reference to the positional relationship of the drawings.

[0019] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. The term "and / or" as used herein includes any and all combinations of one or more of the associated listed items.

[0020] The technical solution of this patent will be further described in detail below with reference to specific embodiments.

[0021] like Figs. 1-2 As shown, this utility model embodiment provides a foaming test kit, including a foaming test kit body 1. The interior of the foaming test kit body 1 is provided with a disinfection pack placement area 2, a fixing strap placement area 3, a three-way device 41 placement area 4, a fixing film placement area 5, a 10ml pre-filled saline solution placement area 6, a 9ml pre-filled saline solution placement area 7, and a 10ml syringe placement area with a spiral interface 8. The top of the foaming test kit body 1 is provided with a disinfection pack placement area 2 and a fixing strap placement area 3. The disinfection pack placement area 2 contains multiple iodine swab packs 21, and the fixing strap placement area 3 contains Velcro fixing straps 31. The middle of the foaming test kit body 1 is provided with a three-way device 41. Placement 4 and fixation membrane placement 5 are provided. Placement 4 contains a combined three-way device 41. Placement 5 contains 511 puncture fixation dressings. The tail of the foaming test pack body 1 is provided with a 10ml pre-filled saline placement 6, a 9ml pre-filled saline placement 7 and a spiral interface 10ml syringe placement 8. Placement 6 contains 3 10ml pre-filled saline syringes 61. Placement 7 contains 3 10ml pre-filled 9ml saline syringes 71. Placement 8 contains 3 10ml syringes 81.

[0022] In the embodiment, the three-way device 41 comprises a main pipe 4101, a first three-way valve 4102, a second three-way valve 4103, a first joint 4104, a second joint 4105, a third joint 4106, a fourth joint 4107, a first locking assembly 4108, a second locking assembly 4109 and a third locking assembly 4110, the first three-way valve 4102 and the second three-way valve 4103 are integrally formed at two ends of the main pipe 4101, the first three-way valve 4102 is provided with the first joint 4104 and the second joint 4105, the first joint 4104 and the second joint 4105 are used for connecting syringes, the first joint 4104 and the second joint 4105 are respectively connected with the first locking assembly 4108 and the second locking assembly 4109, the first locking assembly 4108 and the second locking assembly 4109 are used for locking the syringes, the second three-way valve 4103 is provided with the third joint 4106 and the fourth joint 4107, the third joint 4106 is used for connecting a syringe, the third joint 4106 is connected with the third locking assembly 4110, the third locking assembly 4110 is used for locking the syringe, and the fourth joint 4107 is used for threadedly connecting an intravenous indwelling needle or a stop valve.

[0023] In the embodiment, the tourniquet 9 is placed in the inside of the foaming experiment bag body 1.

[0024] In the embodiment, the straight cannula needle 10 is also placed in the inside of the foaming experiment bag body 1.

[0025] In the embodiment, the Velcro fixing belt 31 is 1 CM.

[0026] In the embodiment, the syringes are all screw syringes, and the screw syringes are matched with the interfaces of the three-way device 41.

[0027] The above embodiments are only used for describing the utility model, and not for limiting the utility model, and the ordinary skilled in the related art can make various changes and modifications without departing from the spirit and scope of the utility model, therefore, all equivalent technical solutions also belong to the scope of the utility model, and the patent protection scope of the utility model should be defined by the claims.

Claims

1. A blister test pack characterized by: The foam experiment package body is internally provided with a disinfection bag placement, a fixing belt placement, a joint three-way device placement, a fixing film placement, a 10ml pre-filled normal saline placement, a 9ml pre-filled normal saline placement and a screw interface 10ml syringe placement, the top of the foam experiment package body is provided with the disinfection bag placement and the fixing belt placement, the disinfection bag placement is internally provided with an iodophor cotton swab bag, the fixing belt placement is internally provided with a velcro fixing belt, the middle of the foam experiment package body is provided with the joint three-way device placement and the fixing film placement, the joint three-way device placement is internally provided with a joint three-way device, the fixing film placement is internally provided with a puncture fixing dressing, the tail of the foam experiment package body is provided with the 10ml pre-filled normal saline placement, the 9ml pre-filled normal saline placement and the screw interface 10ml syringe placement, the 10ml pre-filled normal saline placement is internally provided with three 10ml pre-filled normal saline syringes, the 9ml pre-filled normal saline placement is internally provided with three 10ml pre-filled 9ml normal saline syringes, and the screw interface 10ml syringe placement is internally provided with three 10ml syringes.

2. A blister pack according to claim 1, wherein: The three-way device includes a main pipe, a first three-way valve, a second three-way valve, a first joint, a second joint, a third joint, a fourth joint, a first locking assembly, a second locking assembly and a third locking assembly, the main pipe is integrally formed with the first three-way valve and the second three-way valve at both ends, the first three-way valve is provided with the first joint and the second joint, the first joint and the second joint are used for connecting syringes, the first joint and the second joint are respectively connected with the first locking assembly and the second locking assembly, the first locking assembly and the second locking assembly are used for locking syringes, the second three-way valve is provided with the third joint and the fourth joint, the third joint is used for connecting a syringe, the third joint is connected with the third locking assembly, the third locking assembly is used for locking a syringe, and the fourth joint is used for threadedly connecting an intravenous indwelling needle or a stop valve.

3. A blister pack according to claim 2, wherein: The foam experiment package body is internally provided with a hemostatic tourniquet.

4. A blister pack according to claim 3, wherein: The foam experiment package body is internally provided with a straight cannula needle.

5. A blister pack according to claim 4, wherein: The velcro fixing belt is 1cm.

6. A blister pack according to claim 5, wherein: The syringes are screw syringes, and the screw syringes are matched with the interfaces of the three-way device.

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