CN203937969U - For the transhipment bag of xegregating unit - Google Patents
For the transhipment bag of xegregating unit Download PDFInfo
- Publication number
- CN203937969U CN203937969U CN201420149692.1U CN201420149692U CN203937969U CN 203937969 U CN203937969 U CN 203937969U CN 201420149692 U CN201420149692 U CN 201420149692U CN 203937969 U CN203937969 U CN 203937969U
- Authority
- CN
- China
- Prior art keywords
- bag
- transhipment
- density polyethylene
- xegregating unit
- hdpe
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 25
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims abstract description 18
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 8
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 8
- 238000012856 packing Methods 0.000 description 12
- 230000001954 sterilising effect Effects 0.000 description 8
- 239000003814 drug Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 229940079593 drug Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000013618 particulate matter Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010561 standard procedure Methods 0.000 description 3
- 206010070834 Sensitisation Diseases 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 231100000086 high toxicity Toxicity 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 230000008313 sensitization Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005251 gamma ray Effects 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000010816 packaging waste Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Landscapes
- Packages (AREA)
Abstract
The utility model discloses a kind of transhipment bag for xegregating unit, it comprises a bag, the axis of the affixed annular in sack place of described bag, on described axis, connect a split type butterfly valve, the affixed handle in bottom of described bag, the material of described bag is Low Density Polyethylene, and the material of described axis is high density polyethylene (HDPE), and the material of described handle is high density polyethylene (HDPE).Transhipment of the present utility model bag has advantages of risk easy and simple to handle, effectively to reduce quality safety, be widely used and safety high.
Description
Technical field
The utility model relates to a kind of transhipment bag for xegregating unit.
Background technology
Visible foreign matters, particulate matter and microbes in aseptic injection cause lasting chemical hazard and biohazard to parenteral route medication patient, therefore, at pharmaceutical industry and medical instruments field, the prevention and control of visible foreign matters, particulate matter and germ just become the key link of quality assurance system.In addition, pharmacy corporation, producing some while having high toxicity, high activity, high sensitization class medicine, need to consider how to protect operating personal simultaneously.Based on this, Chinese food Drug Administration (CFDA) explicitly calls for " operation of high pollution risk should complete in isolated operation device " in 2010 editions good practices in the manufacture and quality control of drugs (GMP), simultaneously " article turnover isolated operation device should be paid special attention to prevent to pollute ".
After 2010 editions GMP implement, aseptic medicine and high toxicity, high activity, high sensitization pharmaceutical producing enterprise select to adopt isolator to produce one after another, to replace traditional clean room, so that safer production medicine and more actv. are protected operating personal.
After adopting isolator to produce, pharmacy corporation all runs into a difficult problem, how to import the Medical Packing Materials using in production process into isolator? conventional method is that logical pass-through box or transferring cabin complete at present, there is in this way serious drawback but adopt, specific as follows:
1, operation is extremely loaded down with trivial details, need complete following 5 step operations and can complete transhipment.
(1) open outboard door packing (as plug, aluminium lid, super clean polyethylene sterile bag) are put into cabin;
(2) close outboard door, require to make pass-through box or transferring cabin self-cleaning certain hour according to standard operating procedure (SOP);
(3) open inner side hatch door by gloves, to external packing clean, sterilizing, and require self-cleaning certain hour according to SOP;
(4) material with external packing is taken into isolator, and closed inner side hatch door;
(5) open inner packing by gloves, and plug is poured in equipment and used;
2, there is larger quality safety risk.
(1) packing enter before isolator by pass-through box or transferring cabin, must clean outside face, sterilization treatment, and these operations are often completed by the method for wiping by operating personal, between different operating personnel, there is larger difference, even if same operating personal is also difficult to ensure that each operation is all the same, therefore homogeneity clean, sterilization effect is difficult to ensure; Once clean, sterilizing is not thorough, the particle of its outside face and germ just can pollute the internal environment of xegregating unit, and then affect product design.
(2) if the packing outside face of packaging waste is clean not thorough, also can pollute operation room (clean room of xegregating unit is installed) operating environment, thus harm operator's health.
3, be not suitable for continuous several times transmission.
Each transmission all needs certain for net time, if inadequate from net time, affects product design thereby be easy to cause the air of operation room to enter xegregating unit; Thereby be also easy to cause the air-flow of xegregating unit inside to enter the environment of operation room destruction operation room and then harm operator's health.
Utility model content
The technical problems to be solved in the utility model be in order to overcome complex operation that existing pass-through box or transferring cabin exist, quality safety risk is large and be not suitable for the defect that continuous several times is transmitted, and a kind of transhipment bag for xegregating unit is provided.
The utility model is to solve above-mentioned technical matters by following technical proposals:
A kind of transhipment bag for xegregating unit, its feature is, it comprises a bag, the axis of the affixed annular in sack place of described bag, on described axis, connect a split type butterfly valve, the affixed handle in bottom of described bag, the material of described bag is Low Density Polyethylene, the material of described axis is high density polyethylene (HDPE), and the material of described handle is high density polyethylene (HDPE).
Preferably, described bag is taper, gradually thin towards the sack of described bag by the bottom of described bag.
Positive progressive effect of the present utility model is: (1) is easy and simple to handle: only need three step operations just can realize sterile closed transhipment.(2) effectively reduce the risk of quality safety: Medical Packing Materials is in transport process, and it is independent separately that xegregating unit internal environment, operating personal, operation room environment still keep, and does not have the risk of cross pollution; Therefore fundamentally avoided because packing outside face is clean, sterilizing does not thoroughly produce the risk of polluting.(3) be widely used: transhipment bag of the present utility model can be applicable to multiple fields such as bulk drug transhipment, aluminium lid transhipment, offal treatment, and Applicable scope is extremely extensive.(4) safety is high: because sealing grade is high, the risk that therefore aseptic in whole transport process and particulate matter pollutes is extremely low, very safe.
Brief description of the drawings
Fig. 1 is the structural representation of the utility model preferred embodiment.
Fig. 2 is the schematic diagram that the utility model preferred embodiment is connected with rubber plug cleaning machine.
Fig. 3 is the schematic diagram that the utility model preferred embodiment is connected with xegregating unit.
Detailed description of the invention
Lift a preferred embodiment below, and carry out by reference to the accompanying drawings the clearer the utility model that intactly illustrates.
As shown in Figure 1, a kind of transhipment bag for xegregating unit, it comprises a bag 1, and the axis 2 of the affixed annular in sack place of bag 1 connects a split type butterfly valve 3 on axis 2, the affixed handle 4 in bottom of bag 1, the material of bag 1 is Low Density Polyethylene (LDPE), and the material of axis 2 is high density polyethylene (HDPE) (HDPE), and the material of handle 4 is high density polyethylene (HDPE) (HDPE), bag 1 is taper, gradually thin towards the sack of bag 1 by the bottom of bag 1.
Low Density Polyethylene (LDPE) is a kind of plastic material, and it is applicable to the various forming processs that thermoplastic molding processes, and forming work is good.Bag adopts the LDPE resin material that meets American Pharmacopeia (USP) standard, and therefore, bag is comparatively soft and transparent, and the interior thing of bag is high-visible and can avoid powder to put up a bridge.Can be according to actual needs, take the axis of different size, to be applicable to different interface specifications.Transhipment bag can, through Gamma ray sterilizing, meet aseptic requirement.Bag adopts pyramidal structure, is convenient to pouring out and packing into of article.High density polyethylene (HDPE), English name is " High Density Polyethylene ", referred to as " HDPE ".HDPE is high, the nonpolar thermoplastic base resin of a kind of crystallinity.High density polyethylene (HDPE) is white particle nontoxic, tasteless, odorless, and fusing point is about 130 DEG C, and relative density is 0.941～0.960.It has good resistance to effect of heat and resistance to cold, and chemical inertness is good, also has higher rigidity and toughness, and mechanical strength is good.
Split type butterfly valve generally comprises α valve and the β valve of mutual adaptation.What transhipment bag above connected is the β valve of split type butterfly valve.The present embodiment is taking transhipment plug as example.As shown in Figure 2, the β valve on transhipment bag 10 is connected with the α valve on rubber plug cleaning machine 11, the complete plug of having sterilized enters transhipment bag by valve.Afterwards, valve-off, separates the β valve of also transporting on bag with the α valve on rubber plug cleaning machine.User is carrying transhipment bag by handle.Then, as shown in Figure 3, the β valve on transhipment bag 10 is connected with the α valve on xegregating unit 12, opens valve, and the clean plug after sterilizing is transferred in isolator; Afterwards, valve-off, the β valve on transhipment bag separates with the α valve on xegregating unit.Like this, completed transhipment once.As required, can continuous several times transhipment.
Transhipment bag of the present utility model has the following advantages:
(1) easy and simple to handle: only to need three step operations just can realize sterile closed transhipment.
(2) effectively reduce the risk of quality safety: Medical Packing Materials is in transport process, and it is independent separately that xegregating unit internal environment, operating personal, operation room environment still keep, and does not have the risk of cross pollution; Therefore fundamentally avoided because packing outside face is clean, sterilizing does not thoroughly produce the risk of polluting.
(3) be widely used: transhipment bag of the present utility model can be applicable to multiple fields such as bulk drug transhipment, aluminium lid transhipment, offal treatment, and Applicable scope is extremely extensive.
(4) safety is high: because sealing grade is high, the risk that therefore aseptic in whole transport process and particulate matter pollutes is extremely low, very safe.
Although more than described detailed description of the invention of the present utility model, it will be understood by those of skill in the art that this is only casehistory, protection domain of the present utility model is limited by appended claims.Those skilled in the art is not deviating under the prerequisite of principle of the present utility model and essence, can make various changes or modifications to these embodiments, but these changes and amendment all fall into protection domain of the present utility model.
Claims (2)
1. the transhipment bag for xegregating unit, it is characterized in that, it comprises a bag, the axis of the affixed annular in sack place of described bag, on described axis, connect a split type butterfly valve, the affixed handle in bottom of described bag, the material of described bag is Low Density Polyethylene, the material of described axis is high density polyethylene (HDPE), and the material of described handle is high density polyethylene (HDPE).
2. the transhipment bag for xegregating unit as claimed in claim 1, is characterized in that, described bag is taper, gradually thin towards the sack of described bag by the bottom of described bag.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201420149692.1U CN203937969U (en) | 2014-03-28 | 2014-03-28 | For the transhipment bag of xegregating unit |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201420149692.1U CN203937969U (en) | 2014-03-28 | 2014-03-28 | For the transhipment bag of xegregating unit |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN203937969U true CN203937969U (en) | 2014-11-12 |
Family
ID=51857307
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201420149692.1U Expired - Lifetime CN203937969U (en) | 2014-03-28 | 2014-03-28 | For the transhipment bag of xegregating unit |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN203937969U (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106697349A (en) * | 2017-01-22 | 2017-05-24 | 安及义实业（上海）有限公司 | Powder transferring bag and powder transferring method thereof |
-
2014
- 2014-03-28 CN CN201420149692.1U patent/CN203937969U/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106697349A (en) * | 2017-01-22 | 2017-05-24 | 安及义实业（上海）有限公司 | Powder transferring bag and powder transferring method thereof |
| CN106697349B (en) * | 2017-01-22 | 2022-08-02 | 安及义实业（上海）有限公司 | Powder transfer bag and powder transfer method thereof |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term | ||
| CX01 | Expiry of patent term |
Granted publication date: 20141112 |