CN207768400U - A kind of micro vim and vigour hemostix - Google Patents
A kind of micro vim and vigour hemostix Download PDFInfo
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- CN207768400U CN207768400U CN201720527135.2U CN201720527135U CN207768400U CN 207768400 U CN207768400 U CN 207768400U CN 201720527135 U CN201720527135 U CN 201720527135U CN 207768400 U CN207768400 U CN 207768400U
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- China
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- vim
- vigour
- hemostix
- micro
- connecting rod
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Abstract
The utility model provides a kind of micro vim and vigour hemostix, including：One shell is formed with a connecting seat on the shell, a slideway is formed with inside the connecting seat；The blood taking needle being connect with the shell；One needle seal, including：To be arranged a cap body of the blood taking needle, the blind end (corresponding blood taking needle tip location) of the cap body is embedded with a sealing element, and the side of the cap body is equipped with a gap；It is formed in a first connecting rod of the open end of cap body, the position of the formation other side opposite with the gap in cap body；The second connecting rod that one end is connect by cradle head with the first connecting rod, the second connecting rod can be radially slided along the slideway.After blood sampling, the sealing for completing syringe needle can be facilitated, safety swift to operate, and after the completion of blood sampling, needle seal can quick closure syringe needle, make vim and vigour sample and air exclusion, vim and vigour sample avoided to influence vim and vigour testing result because being communicated with outside air.
Description
Technical field
The utility model is related to medical care field more particularly to medical instruments, and in particular to a kind of micro vim and vigour hemostix.
Background technology
Blood_gas analysis is the gas detected in the presence of blood, it is an important finger for reflecting physiology of respiration function
Mark.Part vim and vigour detect electrolyte (NA, K, CL, CA) and part biochemical project detection combination together at present.Vim and vigour mark
This is to acquire radial artery, preceding brachial artery, based on femoral artery, because only that arterial blood could correctly reflect physiology of respiration function.
Currently, the acquisition of domestic vim and vigour sample mainly has two kinds of modes：Disposable syringe and vim and vigour hemostix (vim and vigour
Needle).Wherein problems with is susceptible to using disposable syringe acquisition vim and vigour sample：
1. complexity：Whether the operation of operating personnel's both hands pricks arteries by rule of thumb when syringe acquires arterial blood,
When operating personnel prick arterial by rule of thumb, another hand starts to draw blood, as arterial is easily pierced through or be extracted by misoperation
Venous blood, acquires old man and child is extremely difficult.
2. patient privacy：Blood collection needle amount is larger (1.5-2ml), mainly (the thigh root artery based on femoral artery
Pipe).
3. pain sense：Pain sense mainly determines that syringe is typically chosen syringe needle by the thickness of syringe needle and blood sampling time length
Between 0.65-0.8, blood sampling volume is in (1.5-2ml) blood sampling time at 10-15 seconds or so.
4. sample variable quantity：Influencing sample result mainly has following factor；
A. blood specimen is wanted and air exclusion, syringe isolation air are preferable.
B. blood specimen temperature, temperature are affected to sample, and syringe blood samples storage time should not surpass under normal circumstances
15 minutes are spent, this is because syringe cannot be quickly cooled down blood specimen, such haemocyte, especially leucocyte and reticulocyte
Continue to be metabolized, generate the acidic metabolites such as lactic acid, PH, BE is made to decline.
C. vim and vigour sample storage material.Syringe is plastic products, and plastic products are more than 15.96kpa in partial pressure of oxygen
(120mmHg) has apparent oxygen consumption, (see Blood_gas analysis and both at home and abroad in relation to vim and vigour book).
5. vim and vigour sample is quantitative：The quantitative finger of vim and vigour sample, the quantitative and blood sampling of anti-coagulants quantify.Syringe anti-coagulants
Number and blood sampling volume completely lean on operating personnel experience, vim and vigour chemical result can be influenced when anti-coagulants is excessive, works as anti-coagulants
It will produce blood coagulation phenomenon when very few.
6. anthemorrhagic difficulty：Since syringe uses thicker syringe needle, larger to vessel injury, bleeding stopping period is longer
(10-15 minutes), are also also easy to produce thrombus.
Thus, at present in medical care field, vim and vigour hemostix (blood gas needle) is generally utilized to acquire vim and vigour sample, can solved certainly
The dynamic blood sampling problem quantitative with blood sampling volume (part is quantitative), that is, solve the problems, such as that anti-coagulants is quantitative, also become acquisition arterial blood
It is simple and convenient.
Existing product, such as the micro vim and vigour hemostix produced by German Roche Diagnostics GmbH is first to cure at home
Protector for collar domain is commonly used to the tool of acquisition vim and vigour sample.Its product structure is as shown in Figure 1 to Figure 3, including blood taking needle 11, shell 12
With needle seal 13.Blood taking needle uses thinner syringe needle, the front end of shell 12 to be formed with female Luer 121, and blood taking needle 11 is logical
It crosses female Luer 121 to connect with shell 12, the structures such as U-shaped capillary of setting in shell.Quantitative trace blood may be implemented.
But there are still some not convenient enough and health places in use for existing product, as shown in Figure 1, product
Before the use, blood taking needle 11 is sealed by needle seal 13, in gnotobasis, when needing blood sampling, by syringe needle
Sealing element 13 is removed, as shown in Fig. 2, then blood was collected, after blood sampling, then covers needle seal 13, is then submitted and is adopted
The vim and vigour sample of collection, and when covering back needle seal 13, since the inner wall of needle seal 13 has been contacted with the external world, destroy
Gnotobasis can influence the parameter of vim and vigour sample to a certain extent；On the other hand, in blood collection procedure, needle seal 13 with
Blood taking needle 11 is separation, cannot arbitrarily be placed so that operation is cumbersome；Also, the syringe needle that blood taking needle 11 uses is very
Sharp, medical staff is when returning needle seal lid, it is possible to since nervous or hasty reason is by needlestick injuries, not only
Personnel's injury is caused, vim and vigour sample but will be polluted.
It is therefore desirable to design a kind of micro vim and vigour hemostix that operation is more convenient, safe, hygienic, to overcome above-mentioned ask
Topic.
Utility model content
In view of the above-mentioned problems, the purpose of this utility model is to provide a kind of micro vim and vigour hemostix, after blood sampling, Neng Goufang
Just complete the sealing of syringe needle, safety swift to operate, and after the completion of blood sampling, needle seal can quick closure syringe needle, make
Vim and vigour sample and air exclusion avoid vim and vigour sample from influencing vim and vigour testing result because being communicated with outside air.
In order to achieve the above object, the technical scheme adopted by the utility model is that：
A kind of micro vim and vigour hemostix, including：
One shell is formed with a connecting seat on the shell, a slideway is formed with inside the connecting seat；
The blood taking needle being connect with the shell；
One needle seal, including：To be arranged a cap body of the blood taking needle, the blind end of the cap body (adopt by correspondence
Blood needle point end position) it is embedded with a sealing element, the side of the cap body is equipped with a gap；
It is formed in a first connecting rod of the open end of cap body, the position of formation is opposite with the gap another in cap body
Side；
The second connecting rod that one end is connect by cradle head with the first connecting rod, the second connecting rod can be along the cunnings
Road radially slides.
Further, there is the other end of the second connecting rod guide post, the guide post outer wall dimension to be equal to or omit
Less than slideway inner wall size；The side of the slideway is formed with retainer with holes, and second connecting rod passes through the retainer with holes.
Further, further include a spring, which is set to the second connecting rod, both ends bear against it is described it is with holes only
Dynamic portion and guide post.
Further, the sealing element is rubber stopper.
Further, the gap length subtracts second connecting rod more than the length of the blood taking needle and is radially slided in slideway
Stroke.
Further, the cradle head is a pin-jointed structure.
Further, the cradle head is a thin-wall construction.
Further, the spring is compression spring.
Further, the blood taking needle is detachably connected by being formed in the female Luer of housing forward end with shell.
Further, the blood taking needle is integrally formed with the shell.
By taking above-mentioned technical proposal, before blood sampling, hold shell on the other hand, another pulls dynamic cap body, then in turn
It is rotated at movable joint, exposes syringe needle, you can blood was collected, after the completion of blood sampling, first rotates according to opposite process and pulls again, then
Under the action of the spring, the guiding for coordinating second connecting rod, pushes back cap body, can be easy to penetrate blood taking needle in sealing element.It can
It is completed within 1 second after blood sampling, the influence of outer bound pair vim and vigour sample is minimized.
Description of the drawings
Fig. 1 is the overall structure diagram of the micro vim and vigour hemostix of existing product in background technology.
Fig. 2 is that the micro vim and vigour hemostix in Fig. 1 removes the structural schematic diagram after needle seal.
Fig. 3 is the structural schematic diagram of the shell of the micro vim and vigour hemostix in Fig. 1.
Fig. 4 is the overall structure diagram of the micro vim and vigour hemostix in one embodiment of the utility model.
Fig. 5 is overall structure diagram of micro vim and vigour hemostix when blood was collected in one embodiment of the utility model.
Fig. 6 is that overall structure when the micro vim and vigour hemostix in one embodiment of the utility model removes blood taking needle is illustrated
Figure.
Fig. 7 is another overall structure diagram of the micro vim and vigour hemostix in one embodiment of the utility model, middle part
Separation structure does section and shows.
Fig. 8 is the partial enlargement structural representation of the micro vim and vigour hemostix in one embodiment of the utility model.
Specific implementation mode
The following will be combined with the drawings in the embodiments of the present invention, carries out the technical scheme in the embodiment of the utility model
Clear, complete description, it is clear that described embodiment is only the utility model a part of the embodiment, rather than whole realities
Apply example.Based on the embodiments of the present invention, those of ordinary skill in the art institute without making creative work
The every other embodiment obtained, shall fall within the protection scope of the present invention.Feature of the cooperation institute's attached drawing to the present invention below
It elaborates with advantage.
As shown in Figures 4 to 6, a kind of micro vim and vigour hemostix is provided in one embodiment, including：
Shell 2 is formed with connecting seat 3 on shell, and with reference to figure 7 and Fig. 8, connection is formed with a slideway inside 3；
The blood taking needle 1 being connect with shell；
Needle seal 4, as shown in fig. 7, comprises：To be arranged the cap body 41 of blood taking needle 1, the blind end of cap body 41 is (right
Answer blood taking needle tip location) it is embedded with rubber stopper 42 as sealing element, the side of cap body is equipped with a gap；
It is formed in the first connecting rod of the open end of cap body 41, the position of the formation other side opposite with gap in cap body；
In addition, the side is also formed with handle 46, it is that can accommodate handle 46 with two fingers and operate pulling or rotating cap body 41.
The second connecting rod 43 that one end is connect by cradle head with first connecting rod, second connecting rod 43 can be radially sliding along slideway
It is dynamic.
There is the other end of second connecting rod 43 guide post, guide post outer wall dimension to be equal to or slightly less than slideway inner wall ruler
Very little, for example, the section of slideway and guide post is circle, then the diameter ratio of the two is 1:0.95~1, other shapes class successively
It pushes away；To smooth sliding；The side of slideway is formed with retainer with holes, and second connecting rod 43 passes through the retainer with holes；
Further include spring 5, be compression spring, spring 5 is sheathed on second connecting rod 43, and both ends bear against retainer with holes and lead
Xiang Zhu.Spring can make the two connection more secured when cap body is set in blood taking needle, and after the completion of blood sampling, by cap body weight
Power-assisted is provided when newly buckling.
In conjunction with aforementioned, the length that gap length is more than blood taking needle 1 subtracts the row that second connecting rod 43 radially slides in slideway
Journey.
Such as figure, cradle head can select a pin-jointed structure, in a further embodiment, can also select and be formed in first
One thin-wall construction of connecting rod and second connecting rod junction.
In conjunction with Fig. 6, blood taking needle 1 can be detachably connected by being formed in the female Luer of 2 front end of shell with shell 2.Another
In outer embodiment, blood taking needle and shell can also be integrally formed and be made.
Such as Fig. 8, before blood sampling, shell is held on the other hand, another hand pulls cap body along the directions arrow S1, is then closed in rotation
It is rotated along the directions arrow S2 at section, exposes syringe needle, you can blood was collected, after the completion of blood sampling, is first rotated again according to opposite process
It pulls, then under the action of the spring, coordinates the guiding of second connecting rod, can be easy to penetrate blood taking needle in sealing element.It can
It is completed within 1 second after blood sampling, the influence of outer bound pair vim and vigour sample is minimized.
Claims (10)
1. a kind of micro vim and vigour hemostix, which is characterized in that including：
One shell is formed with a connecting seat on the shell, a slideway is formed with inside the connecting seat；
The blood taking needle being connect with the shell；
One needle seal, including：To be arranged a cap body of the blood taking needle, the blind end of the cap body is embedded with a sealing
The side of part, the cap body is equipped with a gap；
It is formed in a first connecting rod of the open end of cap body, the position of the formation other side opposite with the gap in cap body；
The second connecting rod that one end is connect by cradle head with the first connecting rod, the second connecting rod can be along the slideway diameters
To sliding.
2. micro vim and vigour hemostix as described in claim 1, which is characterized in that the other end of the second connecting rod has one to lead
Xiang Zhu, the guide post outer wall dimension are equal to or slightly less than slideway inner wall size；The side of the slideway is formed with stop with holes
Portion, second connecting rod pass through the retainer with holes.
3. micro vim and vigour hemostix as claimed in claim 2, which is characterized in that further include a spring, which is set to institute
Second connecting rod is stated, both ends bear against the retainer with holes and guide post.
4. micro vim and vigour hemostix as claimed in claim 3, which is characterized in that the spring is compression spring.
5. micro vim and vigour hemostix as described in claim 1, which is characterized in that the sealing element is rubber stopper.
6. micro vim and vigour hemostix as described in claim 1, which is characterized in that the gap length is more than the blood taking needle
Length subtracts the stroke that second connecting rod radially slides in slideway.
7. micro vim and vigour hemostix as described in claim 1, which is characterized in that the cradle head is a pin-jointed structure.
8. micro vim and vigour hemostix as described in claim 1, which is characterized in that the cradle head is a thin-wall construction.
9. micro vim and vigour hemostix as described in claim 1, which is characterized in that the blood taking needle is by being formed in housing forward end
Female Luer be detachably connected with shell.
10. micro vim and vigour hemostix as described in claim 1, which is characterized in that the blood taking needle and shell one at
Type.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201720527135.2U CN207768400U (en) | 2017-05-12 | 2017-05-12 | A kind of micro vim and vigour hemostix |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201720527135.2U CN207768400U (en) | 2017-05-12 | 2017-05-12 | A kind of micro vim and vigour hemostix |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN207768400U true CN207768400U (en) | 2018-08-28 |
Family
ID=63217871
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201720527135.2U Expired - Fee Related CN207768400U (en) | 2017-05-12 | 2017-05-12 | A kind of micro vim and vigour hemostix |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN207768400U (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105769909A (en) * | 2016-05-13 | 2016-07-20 | 云南舜喜再生医学工程有限公司 | Hemostix and method for directly obtaining cytokine-containing serum |
-
2017
- 2017-05-12 CN CN201720527135.2U patent/CN207768400U/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105769909A (en) * | 2016-05-13 | 2016-07-20 | 云南舜喜再生医学工程有限公司 | Hemostix and method for directly obtaining cytokine-containing serum |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20180828 Termination date: 20190512 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |