DE202014009360U1 - Mixing plant for ready-to-use rinse solutions - Google Patents

Abstract

Mixing unit for ready-to-use rinse solutions, characterized by an RO system (2), a mixing unit (5) which is connected to the RO system (2) and contains a mixing chamber (47), the high-purity water from the RO system (2 ) and rinse solution concentrate from a concentrate source (55) can be supplied, a mobile rinsing solution container, which can be coupled to the mixing unit (5), and a computer and control device (80) for all measuring and monitoring tasks in the on-site production of a rinse solution ,

Description

The aim of this development is to produce a cost-effective, chemically and microbiologically high-purity liquid from tap water locally as a raw material for the use of medical rinsing solutions and to mix it with a concentrate in such a way that larger volumes of ready-to-use rinsing solutions are generated which are mobile to the place of application spent and administered by pressurization.

Both rinsing solutions for endoscopic and general surgical operations, such. As gynecology, urology, arthroscopy by the use of purisole, Ringer, saline concentrates, as well as rinsing solutions for the relief of chronic diseases or for therapeutic applications are produced.

An application of this development for other areas such. As for veterinary medicine, in the laboratory or in biology and in pharmacy as a high purity rinsing fluid or approach medium for the production of drugs, cell cultures and the like is conceivable and practicable.

Medical rinse solutions are usually processed from distilled water as a raw material, which is produced centrally, in a central production process to rinse solutions and brought to the site with significant logistics costs.

The regulatory and normative demands on the quality of the raw material water are so high that it is not yet possible to work on site. B. in the hospital to produce verifiable rinsing solutions on demand.

On the one hand, these are the high microbiological and, on the other hand, the required chemical requirements for the raw material water, which preclude a verifiable and verifiable, normatively required quality of on-site, demand-controlled production.

Although laboratory water devices based on reverse osmosis are available for producing liquid of high chemical and microbiological purity, a disadvantage is the lack of prevention for microbial reduction and a non-verifiable test of the filter stages involved.

For medical use, for example, industrially produced rinsing solutions with volume 3 l, 5 l, 10 l are made available to the hospital and with large in-house, staff logistics inter-u. disposed of.

By way of example, for the duration of the surgery or exam, these bag volumes will not be sufficient for bladder surgery with approximately 60 L of rinse fluid, so a jumper outside the central OR area must be available to provide, warm and deliver the pouches.

The administration takes place partly gravimetrically or with bag pressure cuffs. In addition, often expensive disposable items such as pump segments or for the bag warmer are required.

A significant disadvantage z. As in endoscopic examinations is the lack of visibility through flotating tissue or pulsating rinsing fluid, because, for example, the required rinsing fluid pressure between 0.1 bar to 0.3 bar is not kept constant.

To improve wound hygiene, rinse generously. This causes personnel and material costs.

The decentralized production of medical rinsing solutions by hospital personnel requires safe procedures both in the operation and in the reliability of the technology with regard to the rinsing solution quality.

Necessary improvements, purpose and purpose of this invention are therefore the cost-effective, user-friendly on-site production of a rinsing solution with low personnel and a corresponding to the investigation or several operations rinsing volume.

Of particular importance is the uninterrupted administration without additional additional human effort while maintaining the application temperature and hygiene of the solution with the lowest, normative permissible, microbiological and chemical contamination, without further controls at the site of use.

In this case, a space-saving technique for the preparation of the rinse solution and a mobile rinse solution container are used, which contains the essential components for high hygiene, safety, ease of use and a constant flow and pressure to administer the rinse.

Remaining quantities should be easy to dispose of.

A high availability of the devices in all measuring and monitoring tasks with regard to their intrinsic safety and only a remote probability of failure is important in order to avoid a catastrophic effect on the patient under all circumstances, or the quality or toxicity of the liquid produced in the assured acceptance criteria to monitor.

Also, the filter stage used for the retention of the chemical constituents, preferably as a reverse osmosis membrane, is difficult to diagnose with regard to possible small ruptures.

A conductivity measurement as the sole verification of an osmosis membrane - as used in the prior art - is not sufficient.

Usually, germ reduction in water-bearing systems are performed physically and or chemically. For reasons of toxicity, great effort is required to check the detection after a chemical disinfection because the lowest residual concentrations can lead to serious patient damage.

In addition, the use of chemicals or biocides contaminate the wastewater.

Ideally, a combination should be chosen thermally and chemically to achieve both a cleansing and disinfecting effect.

Due to the resulting higher efficiency, a lower temperature would be required and the concentration of the chemical agent could be lower. However, the practice shows considerable difficulties in terms of the transmembrane flow of a chemo-thermal cleaning solution from the primary to the secondary side of the reverse osmosis membrane, because the high osostic pressure opposes the transmembrane pressure.

Because of the aforementioned difficulties, filters are therefore often used in practice for shorter lives, which are to be replaced after short-term use.

This object is achieved according to the invention effectively in that for the preparation of the rinsing solution, the combination of a reverse osmosis membrane and two further filter stages, for example ultra or sterile filters, preferably as a capillary membrane, are used.

This filter combination and other components are referred to below as the filling station.

To prepare, for example, about 60 l ready-to-use Purisolelösung approximately 56 l sterile-filtered permeate with about 3.6 l highly concentrated Purisolekonzentrat proportional to dilute or mix so that the resulting rinse solution without further tests for intra- and postoperative bladder irrigation for use can come.

The aforementioned rinse solution is representative of z. As for Ringer, and / or other sodium chloride solutions, which can be used in particular in the field of surgery, but also in other medical or mentioned areas. The concentrates and their mixing ratios are to be adapted to the respective applications.

Often used as a rinse solution z. B. 0.9% sodium chloride solutions. For the treatment of approx. 100 l of this solution, a concentrate volume of approx. 2.9 l is sufficient at a ratio of 1:35.

Ringerspüllösungen are to be produced with slight deviations from the above. For example, at a mixing ratio of 1: 34.6 with about 2.872 l of ringer concentrate, 100 l of Ringer's solution must be prepared.

The concentration of about 30-35 times, at a solubility temperature of about 10 ° C shows the potential of logistics, handling and space savings.

However, the described method and the components and volumes used are not reduced to this. Due to the high-purity active ingredients, the exact mixing and dilution, a wide range of rinsing solutions can be produced.

Advantageously, the growth of germs of the concentrate is almost prevented by the high concentration.

For the preparation of the rinsing solution, the concentrate container, which is advantageously designed as a bag, is hung on prepared receptacles of the filling station concentrate scale and the mixing process is initiated. Initially, the balance is verified by the known bag weight.

The Füllstationsseitigen connections of the concentrate as well as the rinsing solution bag to be described will be brought to self-cleaning, foolproof connection connectors of the filling station, which are executed in this application, for example, as flap solutions, but also on the device side can be designed as a flexible hose, brought by the user.

With great advantage, a mobile rinsing solution container, which is preferably designed as a pressure vessel, equipped with an insertable sterile rinsing liquid bag, which is filled with a correspondingly large volume.

The rinsing solution bag contains a permanent connection connector, which can be pushed through and fixed by the lockable lid of the pressure vessel. The connection connector can be provided with continuing flexible hose lines, which are designed as filling or transfer lines. The connector can advantageously also be designed with only one hose, which can be used either as a filling tube or as a transfer tube, depending on the sterility requirements.

For administration of the rinsing liquid at the application site, a transfer system can be connected to the transfer connection of the rinsing solution connector, for example with. connected to an endoscopy system. A connection to other systems commonly used in surgery, for example, to irrigation suction systems is also practicable and possible.

The object of the simple operation and administration with constant purge flow and pressure has been solved by pressurized gas (air) is preferably introduced either into the pressure vessel or optionally directly into the rinsing liquid bag.

In this case, the compressed gas control and monitoring within the mobile flushing solution container is advantageously established. Compressed gas production and feed can be generated for example by an in-house source, but also on the device side.

The proportioning of concentrate and permeate is carried out by means of a concentrate and a rinsing solution container scale, wherein the concentrate balance is verified in the filling station with each attachment of the filled concentrate container.

In addition, the mobile flushing solution container advantageously includes a balance which monitors the filling state and which, for safety reasons, is to be automatically tested by means of reference weight.

For homogenization and temperature control, highly pure or approximately sterile permeate is heated and mixed with added concentrate in a mixing block.

Prior to introduction into a sterile rinse solution / bag, a second sterile filtration of the mixed solution was performed.

The cleaning of the system or germ prevention and reduction by the combination of a low-toxic, based on citrate disinfection u. Detergent with a water heating executed. Wherein both the primary and the secondary side of the reverse osmosis are to be disinfected or cleaned separately by means of an additional pump without transmembrane flow.

In principle, all process-relevant data from both the operating and the protection computer are recorded and possibly calculated. The measurement results are sent from the factory to the protection computer and vice versa. Each computer compares the measurement results with its own and returns a confirmation.

The data are written to the confirmation of operation and protection computer together with a checksum in the trend data memory, which may be preferably designed as Eprom, but also as another storage medium.

The electronics of the mobile rinsing solution tank can be operated by means of rechargeable batteries, on the display of the mobile rinsing solution container all required parameters and their deviations such as weight, temperature and tank pressure are displayed.

By establishing a wireless data exchange between filling station and mobile rinsing solution container, for example, the monitoring of the filling, the proportionality and the temperature takes place.

Further details and advantages are described in the figures shown below.

It shows 1 the basic presentation.

At the same time in the figure, further embodiments and the reference to possible deviations and extensions are executed.

The liquid is transferred via an optional prefiltration ( 1 ) to the RO plant ( 2 ) guided.

For example, the prefiltration with a coarse filter ( 9 ) of a water softening system ( 10 ) a carbon filter ( 11 ) and fine filters ( 12 ). Optionally, the illustrated but unspecified valve circuit is an adjustable differential pressure measurement ( 13 ) over the individual filter stages or a measurement of other components z. B. Chlorine by means of the facilities ( 14 ) possible.

In the entrance area of the RO plant ( 2 ) there is a water inlet valve ( 15 ), an inflow flowmeter ( 16 ) and an input raw water conductivity measurement ( 17 ). The supplied liquid passes through a float-controlled inflow valve ( 18 ) in the supply tank ( 20 ) with level sensors for empty detection and level control ( 19 ) Is provided.

The float-controlled inflow valve ( 18 ) is designed as a membrane servo valve, the servo hole through the lowest buoyancy forces - so very small float volume - can be closed and thus controls the level. In addition, it is possible by means of - not shown - electromagnetic valve to interrupt the servo flow, so as to prevent the feed. Thus, the liquid without significant loss of flow to the flow tank ( 20 ) reach.

The supply tank contains an overflow with detection.

The pump ( 21 ) conveys the liquid to the RO membrane ( 22 ), wherein the retentate via the flow restrictor ( 23 ) with bypass valve ( 24 ) back to the supply tank ( 20 ) to be led.

To adjust the efficiency of the outflow flow meter ( 25 ), which together with the raw water flow meter ( 16 ) determines the efficiency calculation.

Excess or the retentate volume determined from the result of the efficiency calculation is determined via drain valve ( 26 ) to the outflow ( 77 ) and discarded.

To reduce the particles and germs in the retentate flow and for decontamination, an optional centrifugal chamber ( 197 ) with cleaning chamber ( 27 ) intended. Particles in the retentate are collected by the centrifugal force at the bottom of the funnel and from there with an open drain valve ( 26 ) to the drainage. To improve the rinsing process, valve ( 24 ) are opened cyclically.

In addition, through a cleaning chamber ( 27 ) which acts by means of voltage pulses selectable frequencies or magnetic field influences on the liquid, a decontamination or influencing the sparingly soluble calcium and magnesium salts are made so that a deposition of the same on the primary side ( 22.1 ) of the membrane can be largely avoided.

The permeate produced is monitored by the permeate conductivity monitoring ( 31 ) registered. Alternatively, a second redundant conductivity cell ( 46 ) be used.

That through the conductivity measuring cell ( 31 Permeate released by the sterile filter ( 3 ) and the permeate release valve ( 78 ) to the application site via connection ( 167 ) guided.

The permeate return takes place via line ( 32 ). The primary side of the filter ( 3 ) completely overflowed and freed of particle residues.

To generate a permeate pressure, a pressure-maintaining valve ( 199 ) with permeate flush valve ( 34 ) used. Excess permeate reaches this way back to the feed tank ( 20 ).

A chemothermal disinfection begins by the pump ( 35 ) citrate-containing concentrate from storage canister ( 36 ) sucks. Here is the valve ( 39 ), flush valve ( 40 ) and forced ventilation valve ( 37 ) are closed. Ventilation valve ( 37 ) is normally open and can be designed as a spring-loaded hose clamp valve or lift valve. The at security chamber ( 38 ) level sensors (without number) monitor the suction process and thus the level in the storage vessel ( 36 ). Ie. if disinfection is not started or if the canister is empty ( 36 ) there is no disinfectant in the chamber ( 38 ).

With the pump running ( 33 ) the disinfectant / cleaning agent until reaching a predetermined conductivity through the permeate collection tube of the membrane ( 22 ) circulates. In this case, the conductivity concentration via the measuring device ( 31 ) be monitored. It is understood that for receiving the additional liquid valves are to be opened briefly to the drain or to the supply tank. By means of heating ( 28 ) and control sensor ( 29 ) the liquid is warmed up to the desired and preset temperature. Optionally, a chemothermal disinfection of the entire high-purity secondary region ( 22.2 . 3 . 32 ) or the primary area via ( 22.1 ) possible.

If necessary, the open permeate flush valve ( 34 ) heated liquid to the primary circuit ( 22.1 ) to reach the required temperature. Once cleaning solution by means of disinfection device ( 4 ) via feed tank ( 20 ) in the primary circuit ( 22.1 ) of the membrane, the transmembrane flux interrupts. Pump ( 21 ) circulates the primary circuit ( 22.1 ) and cleans or disinfects the entire fluid-carrying components.

After completion of the chemothermal disinfection, a flushing process can be initiated until conductivity cells ( 31 ) or (46) "Disinfectant freedom".

During the flushing process, the disinfection flush valve ( 40 ) to also disinfect the line containing the disinfection unit ( 4 ) to clean.

In order to prevent a subsequent unintentional supply of disinfectant into the permeate circulation ( 32 ) to avoid venting valve ( 37 ) and the levels in chamber ( 38 ) supervised. Thus, a safe avoidance of unintentional disinfection is guaranteed.

In order to initiate a mixing process, it may already be possible for the RO plant ( 2 ) preheated permeate over heater ( 43 ) and temperature controller ( 42 / 44 ) is heated to the required rinse solution temperature. Via line ( 167 ) the permeate of a mixing chamber ( 47 ), into which by means of pump ( 58 ) Concentrate from bag ( 55 ) and line ( 54 ), the connector ( 53 ) and device-side connector ( 49 ) is supplied.

The concentrate flap ( 50 ) opened, detector ( 52 ) reports "open" because magnet ( 51 ) has exceeded the required distance. The concentrate purge valve ( 48 ) only with the flap closed ( 50 ) and according to selected or preset washing programs to open the connection connector ( 49 ) to clean.

Concentrate bag ( 55 ) is with its suspensions ( 56 ) into corresponding hooks of the jib ( 181 ) of the concentrate bag scale ( 57 ).

The second conductivity and temperature measurement ( 46 ) detects the corresponding values for reasons of redundancy. The by chamber ( 47 ) homogeneously mixed and tempered rinsing liquid passes via line ( 166 ) to a second sterile filter ( 59 ). Incorrect flushing liquid is via bypass valve ( 60 ) to the outflow ( 77 ) discarded.

When the valve is closed ( 60 ) and opened flushing solution release valve ( 62 ), the rinsing liquid is applied via the device-side rinse solution connector ( 63 ) the connected bag connector ( 67 ), Management ( 68 ) to the mobile flushing solution container ( 6 ), in which a sterile rinsing solution bag ( 69 ) is inserted. The possibility of taking a sample of rinsing solution consists of sampling ( 61 ).

The mobile flushing solution container ( 6 ) contains a scale ( 71 ), which registers the respective level or the weight of the flush volume. Also is a temperature sensor ( 72 ) is mounted so that the Spülflüssigkeitstemperatur is indirectly measurable.

With closed rinse solution flap ( 64 ) and when selecting and initiating a corresponding wash program, the device-side connector ( 63 ) with sterile liquid or cleaning solution via flushing outflow ( 150 ) rinsed or disinfected.

The integrity test of the filters ( 3 / 59 ) takes place with closed flaps ( 50 / 64 ) by filtered air supply by means of an air pump ( 41 ) and can optionally by valve switching the secondary side of the filter ( 3 ) or the primary side of the filter ( 59 ) apply air. The liquid is partially displaced by the air. Due to the hydrophilic nature of the filter membrane, only a very small pressure drop will take place when the filter characteristic is intact; 45 ) and electronics ( 80 ) can be registered or monitored.

This test allows both the filters ( 3 / 59 ) as well as the tightness of the flaps ( 50 . 64 ) be verified or checked.

The amount of flushing solution in the bag (possibly after use) 69 ) can be obtained by connecting the corresponding line of the bag ( 69 ) at emptying grommet ( 75 ) and switching on the pump ( 76 ) in outflow ( 77 ) are discarded. For this purpose, emptying flap / toggle ( 73 ) open. Flap switch ( 74 ) is activated and switches pump ( 76 ) one.

In 2 schematically is a possible transfer of the rinsing liquid from the mobile rinsing solution container ( 6 ) to an endoscopic system or to the surgical site ( 94 ).

Compressed air connector ( 82 ) can be connected by means of flexible hose lines ( 83 ) are connected to an in-house compressed gas source.

To ensure a constant rinse fluid flow, the pressure control unit ( 81 ) an adjustable pressure regulator ( 84 ), an emergency stop with mushroom button and forced ventilation ( 85 ), a manual pressure relief valve ( 86 ), a pressure gauge display ( 87 ) and an electronic pressure transducer ( 88 ), which, like all sensors and actuators, uses redundant electronics ( 80 ) can be evaluated and displayed.

The low pressure control valve ( 84 ) is adjustable. The pressure control unit ( 81 ) is advantageously designed for a control range of 0 to 0.5 bar and is set for practical use to 0.3 bar delivery pressure, for example, prostate surgery. The regulated air is supplied via hose connection ( 99 ) in pressure vessels ( 97 ).

The rinsing liquid in bags ( 69 ) is supplied by the supplied pressure via transfer port ( 89 ) and a suitable transfer system ( 91 ) to the endoscopic - or other commonly used in surgery system ( 93 ).

In addition, it is noted that between line ( 89 ) and the transfer system ( 91 ) Another sterile filter not shown here would be connectable.

Likewise, it would be possible, the regulated compressed gas medium directly in the flushing solution bag ( 69 ) or completely without pressure control unit ( 81 ) and instead with a suitable pump, the rinsing fluid to the application ( 94 ) to promote. Likewise, an internal air supply is conceivable instead of the external air.

3 spatially illustrates the total unit of a mixing plant or filling station. Due to the assumed confined space in the hospital, the filling station ( 95 ) constructed as flat as possible so as not to impair the passageways in corridors or in premises. This requires a vertical construction of the RO plant ( 2 ) with membrane ( 22 ), Feed tank ( 20 ) and pump ( 21 ). Also shown is a cleaning canister ( 36 ).

Above the RO plant is the mixing unit ( 5 ), in which only the position of the concentrate flap ( 50 ), the flushing solution flap ( 64 ). the heaters ( 28 / 43 ) and the sterile filter ( 3 / 59 ) to clarify handling and construction. Where the flaps ( 50 / 64 ) are shown here in the closed state.

Concentrate bag balance ( 57 ) is below the electronics ( 80 ) and in the form of a cantilever ( 181 ) with holding hooks for the concentrate bag.

The installation is flush with the wall at a suitable location with the appropriate vertical distance to the floor to ensure communication - as explained later - and cleaning.

The mobile flushing solution container ( 6 ) consists of a trolley ( 70 ) with pull and push handle ( 102 ), the pressure vessel ( 97 ), a lid ( 79 ), and an infusion rod ( 98 ).

Components of the mobile flushing solution container ( 6 ) are a pressure control unit ( 81 ), whose output directly via a flexible hose connection ( 99 ) in the pressure vessel ( 97 ) and electronics ( 100 ) with a communication display ( 200 ), for example, to display the level, the temperature, compressed air and other relevant values and a display beam ( 101 ).

The communication between the rinse solution container ( 6 ) and the filling station ( 95 ) takes place wirelessly by means of sensors in the roller area below the bottom plate ( 103 ) of the mobile flushing solution container ( 6 ).

Filling station side is on the same level below the bottom plate of the filling station ( 95 ) attached a corresponding sensor. The detection of the parking or docking positions of the rinse solution container ( 6 ) to the filling station ( 95 ) is determined by the location of the preferred infrared sensors.

The other components are partly explained in the presentation or will be explained later. It is understood that this is a space-saving design of the components, the arrangement may differ from the illustrated or is conceivable in other embodiments. Likewise, not all aspects of the labeling were taken.

4 schematically shows the trolley ( 6 ) or the pressure vessel ( 97 ) with lid open ( 79 ) and a connector receptacle ( 109 ) through which the cylindrical bag connector ( 111 ), and by means of movable connector lock ( 108 ) and holding groove ( 112 ) is held.

To make it a form-fitting seal with good sliding properties between connector ( 111 ) and connector recording ( 109 ), the seal preferably consists of a Teflon insert ( 128 ) with an O-ring ( 127 ) and a pressure plate ( 126 ) so against connector ( 111 ) is pressed, that the aforementioned goals are achieved.

A positive and sealing connection of the lid ( 79 ) to the pressure vessel ( 97 ) is on the one hand by cover sealing ( 107 ) and the conical seal bearing ( 110 ) in the pressure vessel opening in the closed state.

For closing pulls hooks ( 115 ) the lid lock ( 106 ) by means of a locking handle ( 113 ) in position. Locking device ( 114 ) snaps behind the swivel joint ( 116 ) one.

Cover clamping hinge ( 105 ) holds lid ( 79 ) in the open state in an upright position.

It is understood that the bag ( 69 ) is to be introduced into the container.

For vertical support are on the pressure vessel ( 97 ) two lateral guides ( 104 ) with vertical play with chassis ( 70 ) are connected.

The compressed air supply ( 99 ) is attached for example in the hinge area. Connector lock ( 108 ) is in case of failure from the outside via rotary shaft ( 125 ) by means of tools.

Also in this figure, the filling line ( 68 ) with connector ( 67 ), which in the filling process to port ( 63 ) is to connect. After filling, the terminal in the filling line ( 68 ), the mobile flushing solution container ( 6 ) is moved to the place of application and the transfer connection ( 89 ) is with a corresponding transfer system ( 91 ) to connect. Container ( 97 ) is accordingly applied with regulated pressure, so that a continuous, pulsation-free promotion is guaranteed.

For the differentiation of filling line ( 68 ) and transfer line ( 89 ) These are equipped with different connectors and in different lengths, as shown executed.

To illustrate the container scale, the detail A shows a weighing cell ( 71 ), on the one hand on the stable lower part ( 118 ) of the container ( 97 ) and on the other hand on the bottom plate ( 103 ) by means of screws ( 119 ) is positively connected.

Section B shows schematically the test device ( 193 ) of the weighing cell ( 71 ). To pressure vessel ( 97 ) is a test weight intake ( 122 ) appropriate. The spring assisted plunger ( 124 ) of the tension magnet ( 123 ) holds a test weight ( 121 ) at a distance to the test weight intake ( 122 ). Cyclically, the distance of the test weight by switching on the tension magnet ( 123 ), so that the full test weight of weighing cell ( 71 ) is registered. The position of the temperature sensor ( 72 ) as well as a collision protection ( 120 ) are also shown. Transport container ( 6 ) may be equipped with a battery and / or a power supply; Similarly, for heating or for lossless storage of the heated rinsing liquid insulation and / or the addition of a heater preferably as a film heater possible.

It shows the 5 schematically the rinsing solution bag ( 69 ) which consists of a multi-layered, toxicologically harmless material - preferably PE film.

The bag ( 69 ) has a rectangular, welded contour in the one-sided a bag and connector receptacle ( 142 ) circular ( 143 ) is welded into the film. The connector receptacle ( 142 ) is radially on the inside with at least 2 ratchet teeth ( 144 ) into which the connector ( 111 ) is pressed so that a form-fitting, sealing, non-releasable compression ( 145 ) arises. Connector receptacle ( 142 ) is U-shaped and has a collar ( 189 ) for the retaining groove ( 112 ).

The connector ( 111 ) is in 5 executed in two parts, with one-piece, similar geometries are possible within the scope of the invention. In the version shown there is Connector ( 111 ) from a front part ( 130 ), the essential components of which are the hose splices ( 133 ), in which the transfer and filling lines are preferably glued inside and outside, as well as the Einpressanschlag ( 129 ) and the connector ratchet teeth ( 146 ).

For easier insertion into the connector receptacle ( 109 ) of the lid ( 79 ) contains the front part ( 130 ) a bleed ( 132 ). At the back is a picture ( 134 ) for anti-kink protection ( 131 ) of the inner conduits ( 136 / 137 ) intended.

When installed, the bag connector ( 111 ) vertical with connector lock ( 108 ) in Halteut ( 112 ) attached.

With the lid closed ( 79 ) there is a rotation of the bag ( 69 ) by approx. 90 ° against the connector ( 111 ) and thus also a change in the position of the internal transfer ( 137 ) and filling line ( 136 ). The kink protection ( 131 ) includes hose guides ( 135 ), which should prevent a possible kinking of the same.

The transfer line ( 137 ) closes at the lower end with a tube weight ( 138 ), which has contours on all outer sides, on the one hand to complete emptying of the bag compressed foil and to prevent any buoyancy of the transfer line ( 137 ) counteract.

To avoid touch contamination, the connectors ( 67 ) and ( 90 ) Include caps with openings for fumigation for sterility.

The films of the bag ( 69 ) are circumferentially welded (147), that a welding bar of min. greater than 2 mm is present to avoid a rupture.

Already shown in 4 is a possible folding of the bag ( 69 ), which makes easier insertion into the pressure vessel opening ( 110 ).

Where bag ( 69 ) is also executable in other than in the description shown contour or shape.

Moreover, when using an additional pump, not shown in the figures, a circulation of the liquid in the bag via the two terminals of the connector ( 111 ) to improve homogeneity, temperature or liquid already in the bag.

Bag ( 69 ) or bag connector ( 111 ) can also be equipped only with an inner and outer tube, which is to be used both as a transfer and as a filling hose, if there are no hygienic or sterility requirements against it.

6 shows the scheme of a transfer system ( 91 ) which with its connector ( 140 ) to the transfer port ( 90 ) can be adapted and with the conical connector ( 139 ) or a subsequent silicone tube piece ( 93 ) can be connected to an endoscopy or flushing system customary in surgery.

The cone ( 139 ) allows the inclusion of different silicone tube diameters ( 93 ) to connect different system used in surgery.

The hose clamp ( 92 ) may advantageously be designed as a roller clamp for controlling the flushing flow.

The length of the transfer system ( 91 ) can be freely selected and adjusted in its diameter to the desired purge flow, wherein for the system shown a hose inner diameter of about 7 mm was selected.

For reasons of sterility connection ( 140 ) with a gassable cap ( 141 ) equipped.

7 shows in perspective schematically the flushing solution flap ( 64 ), whose opening, closing, excavating and cleaning process is described as follows.

In the flap ( 64 ) there is a magnet ( 65 ), with the flap closed ( 64 ) a magnetic contact ( 66 ) is activated.

For rinsing, the flap ( 64 ), so that the flap latch hook ( 162 ) of the flap lock ( 161 ) in the locking collar ( 163 ) of the connection connector ( 63 ) engages.

By pushing back the lock ( 161 ) via fulcrum ( 158 ) by means of flap locking handle ( 160 ), the locking spring ( 159 ) and the flap locking hook ( 162 ) gives the excavation process of the flap ( 64 ) free. The flap swings upwards. This is supported by excavation spring ( 156 ), the side of the flap pivot ( 155 ) intervenes.

To completely rinse the connector ( 63 ) presses the seal ( 157 ) with closed flap positively on the outer cone ( 164 ) of the connector ( 63 ).

The rinsing fluid passes via connection ( 149 ) over the inner cone ( 154 ) to the washing room ( 153 ) and from there via the circumferentially mounted flushing holes ( 151 ) of the connector ( 63 ) in the annular gap ( 152 ) from which the flushing effluent ( 150 ) he follows.

For reasons of security of confusion for the application, the technical design of the flushing solution connections was designed differently from those of the concentrate connections.

The flushing solution connector ( 63 ) is, for example, with an inner cone ( 154 ) 1 to 16 and a two-start external thread 13 × 8 executed. At the rinse solution bag ( 69 ), which is designed as a disposable item, is the filling line ( 68 ) with one-time connector ( 67 ), which is equipped as a male connector, for example, with freely rotatable union nut with internal thread 13 × 8 and an inner outer cone 1 to 16 so that in the coupled state a positive, sealing connection is ensured by the two cones and thread. In the filling line ( 68 ) a hose clamp can be mounted.

It shows the 8th schematically the concentrate bag ( 55 ) which consists of a, toxicologically harmless material - preferably PE film. The bag ( 55 ) has a rectangular, welded contour.

Bag fillings of about 1-5 liters can cover the commonly used in surgery concentrates and their formulations to produce the required rinse solution.

For connection to the device-side connector ( 49 ), the connection hose ( 54 ) be executed in different lengths. Bag ( 55 ) with its suspension openings ( 56 ) in the boom ( 181 ). Boom ( 181 ) has a z-shaped bend and is for stiffening and positive connection with outbreak ( 179 ) by means of screws ( 180 ) on bending beam ( 178 ) attached. The bending beam ( 178 ) is with its rear end with a support arm ( 176 ), which in turn is connected to the rear wall ( 175 ) of the filling station ( 95 ) adjustable by means of adjusting screw ( 177 ) connected is.

It is understood that at the beginning of the mixing process, the sterile cap ( 174 ) and the crushing cone ( 198 ) is to break. Filling connection ( 172 ) is welded.

The function of the concentrate flap ( 50 ) as well as the concentrate feed from bag ( 55 ) via pump ( 58 ), the mixing process and the rinsing process were already in 1 described. The flap function is equal to the already described function of the flushing flap.

9 shows schematically and in perspective the emptying of the rinse solution bag ( 69 ) and the structure of the outflow block ( 185 ).

Overall, the outflow block ( 185 ) four outlets, all in a siphon / outflow ( 77 ). Gutter ( 182 ) is used to catch residual fluids that could arise when connecting the bag or opening the flaps.

To prevent burns or chemical burns, a splash guard ( 186 ) into the gutter ( 182 ) that the drains are covered, but via the test opening ( 187 ) a residue sample is possible. Recognizable in the sectional view is the emptying flap ( 73 ), which by means of a pinning ( 192 ) on a rotary shaft ( 191 ) is attached. The emptying flap ( 73 ) includes a blind bore with internal seal ( 190 ). In the closed state of the flap ( 73 ), the seal is located on the front side of the emptying grommet ( 75 ). To open flap ( 73 ) pulled forward and swung upwards. This will make switch cam ( 195 ) of the drain switch ( 196 ) free and pump ( 184 ) starts to suck. At the same time, return spring ( 194 ) biased because flap ( 73 ) in the swung-out state receives a holding position, the rotary shaft ( 191 ) at a distance to the switch cam ( 195 ) holds.

To close and stop the emptying process, flap ( 73 ) returned to their original position. Return spring ( 194 ) positions the seal ( 190 ) positively on the spout ( 75 ). At the same time, switch ( 196 ) or switching cam ( 195 ) again. Legend 1 Pre-filtration 2 RO system 3 Permeate Ultra / Sterile Filter 1 4 disinfection unit 5 mixing unit 6 Dolly 7 emptying 8th Air pressure supply 9 coarse filter 10 softeners 11 carbon filter 12 fine filter 13 pressure measurement 14 Chlorine / calcium measurement 15 Water inlet valve 16 flowmeter 17 Conductivity / temperature display 18 float valve 19 level sensor 20 feed tank 21 Booster pump 22 RO membrane 22.1 primary 22.2 secondary side 23 High-pressure reactor 24 Bypass valve 25 Drain flowmeter 26 drain valve 27 cleaning chamber 28 Heating permeate circuit with overtemperature protection 29 thermostat 30 Permeatverbesserung 31 Conductivity Probe 32 permeate 33 Permeatzirkulationspumpe 34 permeate flush 35 disinfection pump 36 Disinfectant canister 37 vent valve 38 Safety chamber with level detectors 39 Disinfection release valve 40 Desinfektionsspülventil 41 Compressed air pump 42 thermostat 43 Heating with overtemperature protection 44 thermostat 45 pressure sensor 46 Redundant conductivity / temperature measurement 47 mixing chamber 48 Konzentratspülventil 49 Device-side concentrate connection connector 50 Concentrate port door 51 magnet 52 Magnetic sensor 53 Concentrate bag connector with crushing cone with 2-way external thread and inner cone 54 Concentrate connection cable 55 concentrate bag 56 Aufhängösen 57 concentrate balance 58 concentrate pump 59 Sterile filter 2 60 Spüllösungsbypassventil 61 Sampling valve 62 Spüllösungsfreigabeventil 63 Device-side flushing solution connection connector 64 Spüllösungsklappe 65 magnet 66 Magnetic sensor 67 Spüllösungsbeutelanschlusskonnektor 68 filling line 69 Spüllösungsbeutel 70 chassis 71 Spüllösungsbehälterwaage 72 temperature sensor 73 Emptying flap / gag 74 fold detector 75 drain connection 76 drain pump 77 outflow 78 Permeatfreigabeventil 79 Lid rinse solution container 80 electronics 81 Pressure control device 82 Compressed air connector 83 hose extension 84 pressure regulator 85 Emergency stop with ventilation 86 Pressure relief valve 87 manometer 88 pressure sensor 89 transfer line 90 transfer connector 91 transfer system 92 clamp 93 Connection for surgery equipment 94 Surgical area 95 filling station 96 Display keyboard / printer 97 pressure vessel 98 IV pole 99 Air connection hose 100 Dolly electronics with display 101 traffic light 102 push handle 103 baseplate 104 Lateral stabilization pressure vessel 105 Clamping hinge cover 106 lid lock 107 cover gasket 108 Locking bag connector 109 Connector receptacle with internal mechanical seal 110 Container opening with conical seal holder 111 bag connector 112 Groove bag connector 113 locking handle 114 locking safety 115 Hook locking handle 116 swivel 117 Lid-lifting handle 118 Bottom plate pressure vessel 119 mounting screws 120 Shipping bolts 121 test weight 122 Test weight recording 123 pull magnet 124 lifting spring 125 Locking rotary shaft with hexagon socket 126 printing plate 127 O-ring 128 Teflon insert 129 Stopper bag connector 130 Bag connector front part 131 Bag connector kink protection 132 Konnektoreinführfase 133 Hose splices 134 Recording kink protection 135 hose guide 136 Internal filling line with optional non-return valve 137 Inner transfer line 138 Weight 139 Cone grooved (5-10 mm) 140 Patient connector with union nut 141 Gas inlet cap / contact protection 142 connector receptacle 143 Circular Folienanschweißstelle 144 Ratchet teeth connector receptacle 145 Konnektorverpressung 146 Ratchet teeth pouch connector 147 Peripheral bag welding 148 bag labeling 149 rinse solution conduit 150 Spüllösungsspülleitung 151 Peripheral flushing hole 152 annular gap 153 Wash cabinet 154 Internal cone flushing connector 155 Flaps pivot point 156 excavation spring 157 flap seal 158 Locking pivot 159 Verriegelungsrückholfeder 160 locking handle 161 lock 162 Door locking latches 163 locking collar 164 Sealing abutment 165 Konzentratspülleitung 166 rinse solution conduit 167 Permeatversorgungsleitung 168 Excavation spring concentrate flap 169 Fulcrum concentrate flap 170 Locking concentrate flap 171 Locking collar Concentrate flap 172 Filling connector 173 labeling 174 cap 175 Filling station rear wall 176 Boom attachment for scale cell 177 Adjustment screw for scale cell 178 Bending-beam load cell 179 outbreak 180 mounting screws 181 Concentrate balance boom with bag hook 182 gutter 183 siphon 184 drain pump 185 drain block 186 splash guard 187 sample opening 188 Connection spout for drain pump 189 Covenant for holding 190 Seal emptying grommet 191 Rotary shaft emptying flap 192 Securing lock rotary shaft 193 Test device weighing cell 194 Return spring for discharge flap 195 switch cam 196 drain switch 197 centrifugal 198 crushing cone 199 Permeate pressure holding valve 200 Display of mobile flushing solution container

Claims (11)

Mixing plant for ready-to-use rinsing solutions, characterized by a RO plant ( 2 ), a mixing unit ( 5 ) with the RO system ( 2 ) and a mixing chamber ( 47 ) contains high-purity water from the RO plant ( 2 ) and rinse solution concentrate from a concentrate source ( 55 ), a mobile rinse solution container, which is connected to the mixing unit ( 5 ), and a computer and control device ( 80 ) for all measuring and monitoring tasks during on-site production of a rinse solution. Mixing plant according to claim 1, characterized in that the RO plant ( 2 ) a disinfection unit ( 4 ) with a pump ( 35 ) connected to the secondary circuit of the RO membrane ( 22 ) is connected and their disinfecting and cleaning agent can be distributed in the primary circuit. Mixing plant according to claim 1 or 2, characterized in that a permeate supply line ( 167 ) of the mixing unit ( 5 ) with the secondary side of a permeate sterile filter ( 3 ) of the RO plant ( 2 ) and a permeate release valve ( 78 ) having. Mixing plant according to claims 1 to 3, characterized in that the concentrate source is a concentrate bag ( 55 ), which is filled with a concentrate balance ( 57 ) connected is. Mixing plant according to claims 1 to 4, characterized in that the concentrate bag ( 55 ) via a concentrate bag connector ( 53 ) with a device-side concentrate connection connector ( 49 ) is connectable. Mixing plant according to claims 1 to 5, characterized in that the rinsing solution container a rinsing solution bag ( 69 ) contained in a pressure vessel ( 97 ) is arranged. Mixing plant according to claims 1 to 6, characterized in that the flushing solution bag ( 69 ) via a flushing solution connection connector ( 67 ) with a device-side flushing solution connection connector ( 63 ) is connectable. Mixing plant according to claims 1 to 7, characterized in that the device-side connection connectors ( 49 . 63 ) Are flaps which are switched on in disinfection circuits. Mixing plant according to claims 1 to 8, characterized in that the pressure vessel ( 97 ) on a chassis ( 70 ), which is a rinsing solution container balance ( 71 ) and a temperature sensor ( 72 ) contains. Mixing plant according to claims 1 to 9, characterized in that the rinsing solution bag ( 69 ) with a transfer line ( 89 ) and a transfer connector ( 90 ) is provided for connection to a transfer system ( 91 ), which contains a connection for a surgical device. Mixing plant according to claims 1 to 10, characterized in that the flushing solution bag ( 69 ) via a filling line ( 68 ) with a connection connector of a drain block ( 185 ) is connectable.

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