Patent Application
20250235610
This disclosure relates to a filling apparatus for filling a reusable reservoir of a medical dispensing device. The filling apparatus has a receiving portion that is configured for holding a reusable reservoir of a medical dispensing device, a supply container that is configured for containing a liquid medication, a first connection port that is configured for fluidly connecting an inner volume of the reusable reservoir of a medical dispensing device with the supply container, and a sterilization device that is configured for sterilizing the inner volume of the reusable reservoir of a medical dispensing device.
A hitherto known medical dispensing device has a reservoir that is configured for containing a liquid medication. During use of the medical dispensing device, the liquid medication is dispensed out of the reservoir through an opening therein and administered to a patient. However, after being depleted, the empty reservoir is disposed, thereby increasing an amount of waste and in turn stressing the environment.
When providing a reusable reservoir instead of a disposable reservoir, less waste is created. However, care has to be taken that refilled reservoir can unproblematically be used and, for example, not contaminated, which may harm a user of the medical dispensing device.
U.S. Pat. No. 8,839,828 B2 discloses a system for filling a reusable medical reservoir of a medication dosing apparatus. Said filling device further includes a purification device that allows a sterile cleansing of the reusable medication reservoir before refilling it with medication. For sterile cleansing, a cleansing agent, such as an isotonic table salt solution or an alcoholic solution, is provided in a container or supply tank of the filling apparatus. This design has the disadvantage that a residual amount of medication and/or a residual amount of the cleansing agent may remain in the reusable medical reservoir after being cleaned. When refilling the medical reservoir, the residual amount of cleansing agent and/or residual amount of liquid medication is mixed with the newly filled medication. This lowers the quality of the refilled reusable medical reservoir and makes refilling of the reusable medical reservoir less attractive to a user.
This disclosure teaches a filling device that avoids at least one of the problems associated with filling apparatuses known from the prior art. In particular, this disclosure teaches an improved filling apparatus for sterilizing a reusable reservoir of a medical dispensing device.
According to a first aspect, a filling apparatus for filling a reusable reservoir of a medical dispensing device is provided. The filling apparatus comprises a receiving portion that is configured for holding a reservoir of a medical dispensing device, a supply container that is configured for containing a liquid medication, a first connection port that is configured for fluidly connecting an inner volume of the reusable reservoir of a medical dispensing device with the supply container, and a sterilization device that is configured for sterilizing the inner volume of the reusable reservoir of a medical dispensing device. The filling apparatus further comprises a discharging device that is configured to discharge deposit, during use of the filling apparatus, from of the reusable reservoir of the medical dispensing device. The discharging device is configured for fluidly connecting the inner volume of the reusable reservoir of a medical dispensing device with the discharging device. The sterilization device comprises a radiation chamber that is configured for housing the reusable reservoir of a medical dispensing device. The radiation chamber comprises an access opening that is configured to be opened and closed, and a protective barrier that is configured to hinder radiation from leaving the radiation chamber. The sterilization device further comprises a radiation source that is configured for providing radiation within the radiation chamber.
During use, a reusable reservoir is inserted into the radiation chamber of the filling apparatus via the access opening of the radiation chamber. The access opening of the radiation chamber is configured so that it can be opened and closed for placing the reusable reservoir in the radiation chamber and for removing the reusable reservoir from the radiation chamber. The sterilization device can further comprise a safety-mechanism, for example, a safety-switch, that hinders radiation spreading within the radiation chamber when the access opening of the radiation chamber is open. The safety-mechanism can switch-off and/or hinder activation of the radiation source in case the access opening of the radiation chamber is open so not to generate radiation and/or so as not to provide radiation to the radiation chamber. The safety-mechanism increases the safety of organisms and the environment near the filling apparatus by preventing at least an excessive exposure of the organisms and the environment to radiation leaving the radiation chamber.
When being placed in the radiation chamber, the reusable reservoir is brought into engagement with the receiving portion. The receiving portion holds the reusable reservoir in a predetermined position within the radiation chamber. The connecting port is coupled to an opening of the reusable reservoir, thereby fluidly connecting the inner volume of the reusable reservoir to a supply container. The supply container is configured for storing a liquid medication so that the reusable reservoir can filled or refilled, respectively, with liquid medication from the supply container. Liquid medication in the context of this disclosure refers to a liquid drug or pharmaceutically effective solution. For instance, the liquid medication can be insulin, or a solution containing insulin.
By way of example only, the supply container can be a replaceable supply container and/or a refillable supply container that is fixedly integrated into the filling apparatus. The replaceable container can be disposable or reusable. A replaceable, disposable supply container can comprise a tamper-evident closure indicating a first-time opening or first-time use of the disposable supply container. Alternatively or in addition, the tamper-evident closure of the disposable supply container can hinder a refilling of the disposable supply container. These designs of a supply container help to provide a larger amount of liquid medication for filling and refilling a reusable reservoir of a medical dispensing device in a safe and convenient way. A tamper-evident closure further improves the patient's safety by hindering use of a fraudulent/manipulated user reservoir.
After use of the reusable reservoir and its depletion by a medical dispensing device, deposit can still be present in the reusable reservoir. Thus, before refilling the reusable reservoir, deposited material that may be contained in the reusable reservoir is removed from the reusable reservoir by the discharging device of the filling apparatus. In the context of this disclosure, deposit (deposited material) refers to one or more of a residual amount of liquid medication, a residual amount of a cleansing agent, a residual amount of bodily fluids, and/or a residual amount of contaminations in the reusable reservoir as well as combinations thereof.
The radiation chamber is part of the sterilization device included in the filling apparatus and comprises a protective barrier that is configured to hinder radiation from leaving the radiation chamber. The protective barrier helps to protect persons positioned the filling apparatus, in particular a user of the filling apparatus, against radiation that, during use of the sterilization device, is generated by the radiation source for sterilizing the reusable reservoir. The protective barrier limits the presence of radiation outside the filling apparatus that is generated by the radiation source and that may otherwise harm the user of the filling apparatus or the environment close to the filling apparatus. The selection of the radiation source is tuned to the selection of the protective barrier, and vice versa. For instance, the radiation source can comprise or form a source for UV-C radiation and/or a source for gamma radiation and/or source for X-ray radiation. Accordingly, the protective barrier can be configured to hinder the respective UV-C radiation and/or gamma radiation and/or X-ray radiation that, during use of the filling apparatus, is provided by the radiation source passing the protective barrier of the radiation chamber.
In the meaning of this disclosure, UV-C radiation refers to an electromagnetic wave having a wavelength in the range between equal to or more than 100 nm and equal to or less than 280 nm. In a variant, the radiation source is configured to generate UV-C radiation in the range between equal to or more than 265 nm and equal to or less than 270 nm. According to an embodiment, the radiation source is configured to provide a median radiation efficiency of UV-C radiation within the radiation chamber in the range between equal to or more than 10 J/m2 and equal to or less than 450 J/m2. Alternatively, the median radiation source is configured to provide a median radiation efficiency within the radiation chamber in the range between equal to or more than 10 J/m2 and equal to or less than 50 J/m2.
A source for gamma radiation, in the meaning of this disclosure, is a radiation source that is configured for providing an electromagnetic wave having a wavelength equal to or less than 0.005 nm and more than 0 nm.
A source for X-ray radiation, in the meaning of this disclosure, is a radiation source that is configured for providing an electromagnetic wave having a wavelength in the range between equal to or more than 0.1 nm and equal to or less than 10 nm.
According to an embodiment, the respective radiation source is configured to provide a median radiation dose within the radiation chamber which is necessary to achieve a sterility assurance level of 10−6, meaning that after the sterilizing of the reservoir within the radiation chamber, only one or less microorganisms out of one million microorganisms of the germ Bacillus pumilus remain active. The median radiation dose within the radiation chamber describes the absorbed radiation dose necessary to achieve the aforementioned sterility assurance level of 10−6. For example, a respective radiation source is configured to provide a median radiation dose of UV-C radiation and/or of gamma radiation and/or X-ray radiation within the radiation chamber in the range between equal to or more than 25 kJ/kg and equal to or less than 32 kJ/kg.
According to an embodiment, the protective barrier is integrated into housing elements forming the radiation chamber. Alternatively or in addition, the protective barrier forms the housing elements of the radiation chamber or forms at least a circumferential layer of the housing elements of the radiation chamber. In the meaning of this disclosure, housing elements, inter alia, refer to wall elements and door elements defining a closed dosing chamber. “Closed” in the context of this disclosure does not exclude presence of supply lines, connectors and tubing for operating the radiation chamber as a component of the filling apparatus. Hindering radiation from leaving the closed radiation chamber is achieved when the respective median radiation dose of the radiation as generated by the respective radiation source is outside of the radiation chamber at a distance of 1 cm from the closed access opening of the radiation chamber less than 5%, preferably less than 1%, of the median radiation dose inside of the radiation chamber.
The radiation source can be housed within the radiation chamber or be placed outside the radiation chamber. When being placed outside the radiation chamber, the radiation source can comprise an additional protective barrier hindering radiation from leaving the filling apparatus. In any event, the sterilizing device is configured such, that during use of the filling apparatus, radiation originating from the radiation source is spread within the radiation chamber for sterilizing the reusable reservoir.
A medical dispensing device is a device for dispensing a medication, preferably liquid medication, to a patient. By way of example, the medical dispensing device can be a medical infusion pump for infusing liquid medication into a patient's body. A medical infusion pump, for example, can be a body-wearable infusion pump. Accordingly, a reusable reservoir of a medical dispensing device can be a reusable reservoir of a medical infusion pump. In an embodiment, the medical dispensing device is an insulin patch pump, and the reusable reservoir is a reusable reservoir of the insulin patch pump.
In an embodiment, the discharging device comprises a waste container that is configured for storing deposit that during use of the discharging device is discharged from the reusable reservoir of a medical dispensing device. For example, the waste container is a removable and disposable container. Deposit discharged from the reusable reservoir is stored in the waste container and thus can be disposed together with the waste container in a clean and sterile manner.
The filling apparatus can further comprise a drive mechanism (also referred to herein as “drive”) that is configured for actuating a discharging mechanism of the reusable reservoir. For instance, a discharging mechanism of a reusable reservoir can comprise a plunger that is movably arranged within the inner volume of the reusable reservoir, wherein upon moving the plunger within the reusable reservoir, the inner volume can be increased or decreased. Upon decreasing the inner volume of the reusable reservoir, deposit or content within the reusable reservoir is discharged from the reusable reservoir, for instance, into the waste container of the discharging device. Likewise, when increasing the inner volume of the reusable reservoir, liquid medication can be conveyed from the supply container via the connection port into the reusable reservoir.
In an embodiment, the discharging device comprises a heating module (also referred to herein as “heater”) that is configured for evaporating deposit in the inner volume of the reusable reservoir of the medical dispending device. For example, the heater can comprise a heating coil and/or a heat lamp. Once deposit is evaporated by the heating module, during use of the filling apparatus, the evaporated, and thus, gaseous deposit can be easily discharged from the reusable reservoir.
According to an embodiment, the first connection port is configured for alternately fluidly connecting the inner volume of the reusable reservoir with the supply container and fluidly connecting the inner volume of the reusable reservoir with a waste container of the discharging device. The connection port can comprise a valve that is configured to be operated in a discharging state and a supply state. In the discharging state, the valve of the connection port fluidly connects the inner volume of the reusable reservoir to the waste container. In the supply state, the valve of the connection port fluidly connects the inner volume of the reusable reservoir to the supply container. A connection port comprising a valve that is configured for alternately fluidly connecting the inner volume of the reservoir to either a waste container or a supply container helps to provide a compact and simple to use filling apparatus.
The filling apparatus can further comprise a cleansing agent container that is configured for containing a cleansing agent for cleansing a reusable reservoir of a medical dispensing device. During use of the filling apparatus, the cleansing agent container is fluidly connected to the inner volume of the reservoir. For example, a cleansing agent can be one or more of isopropyl alcohol, ethanol, distilled water, or ethylene oxide gas.
If respectively present, the supply container and/or the waste container and/or the cleansing agent container can be fluidly connected to the first connection port, so that, during use of the filling apparatus, the respective containers are fluidly connected to the inner volume of the reusable reservoir by the first connection port. For alternately fluidly connecting the respective container to the inner volume of the reusable reservoir, the first connection port can comprise a valve that is configured for alternately fluidly coupling one at time of the respective containers to the inner volume of the reusable reservoir. Alternatively, the filling apparatus can comprise a second connection port that is configured for fluidly connecting the waste container to the inner volume of the reusable reservoir and/or a third connection port that is configured for fluidly connecting the cleansing agent container to the inner volume of the reusable reservoir. Likewise, the reusable reservoir can comprise a first opening that is configured for coupling the inner volume of the reusable reservoir to the first connection port. In addition, the reusable reservoir can comprise a second opening that is configured for coupling the inner volume of the reusable reservoir to the second connection port. The second connection port can be configured to fluidly couple the inner volume of the reusable reservoir via the second opening of the reusable reservoir to a waste container and/or the cleansing agent container. Further in addition, the reusable reservoir can comprise a third opening that is configured for coupling the inner volume of the reusable reservoir to the third connection port. The third connection port can be configured to fluidly couple the inner volume of the reusable reservoir via the third opening of the reusable reservoir to a cleansing agent container.
In an embodiment, the cleansing device and the discharging device are fluidly connected to the inner volume of the reusable reservoir by two different connection ports. For example, the cleansing agent container can be fluidly connected to the inner volume of the reusable reservoir via the first connection port, while the waste container of the discharging device is fluidly connected to the inner volume of the reusable reservoir via the second connection port. During use of the filling apparatus, the inner volume of the reusable reservoir is flushed with a cleansing agent provided by the cleansing agent container through one of the two connection ports, while cleansing agent is removed from the inner volume of the reusable reservoir via the other of the two connection ports. Thereby, a direction of flow of the cleansing agent is achieved within the inner volume of the reusable reservoir from one connection port to the other connection port. For example, during use, cleansing agent from the cleansing agent container is flowing through the first connection port into the inner volume of the reusable reservoir and from the inner volume of the reusable reservoir via the second connection port into the waste container. A flow of cleansing agent within the inner volume of the reusable reservoir from one connection port to another connection port allows a continuous flow of cleansing agent through the reservoir that can sweep along gas bubbles and deposit out of the inner volume of the reservoir. In an embodiment, the two connection ports are arranged such that in a state in which the filling apparatus is placed on a table ready-for-use, the connection port fluidly connected to the cleansing agent container is closer to the geo center than the connection port fluidly connected to the waste container. Thereby, the flow of cleansing agent within the inner volume is directed at least in part against gravity, such that gas bubbles that may be contained in the inner volume of the reusable reservoir during cleansing of the inner volume are already naturally tending to rise in the direction of the connection port fluidly connected to the waste container.
According to an embodiment, the filling apparatus further comprises a charging device (also referred to herein as “charger”) for charging a rechargeable battery of a reusable reservoir and/or for charging a rechargeable battery of a medical dispensing device. The filling apparatus can comprise a docking station that is configured for electrically connecting the charging device to a rechargeable battery of a medical dispensing device.
This disclosure further relates to medical dispensing device system comprising a reusable reservoir for a medical dispensing device, and a filling apparatus for filling the reusable reservoir of a medical dispensing device, the filling apparatus comprises:
In an embodiment, the reusable reservoir comprises an opening that is configured for fluidly connecting the inner volume of the reusable reservoir to the first connection port. The reusable reservoir can further comprise a removable plug portion comprising a septum, when being inserted into the opening the plug portion sealing the opening fluidly tight, but still allowing access to the inner volume of the reusable reservoir through the septum, for instance, by a connecting needle of the medical dispensing device. When being removed, the at least one opening allows access to the inner volume of the reservoir via the first connection port.
The reusable reservoir can be a reusable reservoir of a body-wearable insulin infusion pump, such as, for example, an insulin patch pump, wherein the medical dispensing device system comprises a medical dispensing device that is a body-wearable insulin infusion pump. In an embodiment, the radiation chamber is configured to house the body-wearable insulin infusion pump alone or in a state separate from the reusable reservoir or in a state including the reusable reservoir.
According to an embodiment, the radiation source of the filling apparatus of the medical dispensing device system comprises or is one or more of a source for UV-C radiation, a source for gamma radiation or a source for X-ray radiation, wherein the reusable reservoir is configured to be transparent for the respective radiation provided by the radiation source. Transparent for the respective radiation provided by the radiation source in the meaning of this disclosure means that when the radiation provided by the radiation source encounters the reusable reservoir, almost all, preferably at least 70%, of the radiation passes through the reusable reservoir into the inner volume of the reusable reservoir. In an embodiment, the reusable reservoir is at least partially made from glass and/or a transparent plastic material that is transparent for electromagnetic waves having a wavelength in the range from equal to or larger than 400 nm and equal to or less than 780 nm. This designs not only allows visible inspection of the inner volume of the reservoir by a human eye, but also allows radiation generated by the respective radiation source to reach the inner volume of the reservoir by passing the material of the reusable reservoir.
Insofar as in the foregoing as well as in the following detailed description of embodiments and claims of a filling apparatus for filling a reusable reservoir reference is made to a filling apparatus or to a reusable reservoir of a medical dispensing device, the characteristics described thereof are also applicable for the filling apparatus as part of a medical dispensing device system or for the reusable reservoir as part of a medical dispensing device system, respectively.
This disclosure further relates to a method for filling a reusable reservoir of a medical dispensing device, the method is constituted to be executed by a filling apparatus of this disclosure, the method comprises the steps of:
First, deposit that may still be contained in the inner volume of the reusable reservoir is removed by the discharging device of the filling apparatus. The deposit is discharged from the inner volume of the reusable reservoir into the waste container so that it can be disposed in a clean and simple way. The then emptied reusable reservoir is sterilized by sterilizing the inner volume of the reusable reservoir by providing radiation within the radiation chamber by the radiation source of the sterilization device of the filling apparatus. Afterwards, the inner volume of the reusable reservoir is filled with liquid medication from the supply container of the filling apparatus via the first connection port of the filling apparatus.
The method for filling a reusable reservoir of a medical dispensing device can further comprise the step of evaporating residual deposit in the inner volume of the reusable reservoir by a heating module of the filling apparatus.
Optionally, the method for filling a reusable reservoir of a medical dispensing device can comprise the step of cleansing the inner volume of the reusable reservoir by flushing the inner volume of the reusable reservoir with a cleansing agent provided by a cleansing agent container of the filling apparatus. Flushing the inner volume of the reusable reservoir helps to completely remove residual deposit from the inner volume of the reusable reservoir, and, thus, helps to provide a safely reusable reservoir.
In an embodiment, the method for filling a reusable reservoir of a medical dispensing device comprises the step of charging a rechargeable battery of the reusable reservoir and/or charging a rechargeable battery of a medical dispensing device by a charging device of the filling apparatus.
Insofar as in the foregoing as well as in the following detailed description of embodiments and claims of a method for filling a reusable reservoir of a medical dispensing device by a filling apparatus of this disclosure reference is made to a filling apparatus or to a reusable reservoir of a medical dispensing device, the characteristics described thereof are respectively applicable for the filling apparatus alone and as part of a medical dispensing device, or the reusable reservoir alone and as part of a medical dispensing device.
The above-mentioned aspects of exemplary embodiments will become more apparent and will be better understood by reference to the following description of the embodiments taken in conjunction with the accompanying drawings, wherein:
The embodiments described below are not intended to be exhaustive or to limit the invention to the precise forms disclosed in the following detailed description. Rather, the embodiments are chosen and described so that others skilled in the art may appreciate and understand the principles and practices of this disclosure.
The medical dispensing device system 1 further comprises a pump base (not shown) that together with the reusable reservoir 2 form a medical dispensing device 3 (not shown).
The filling apparatus 1a comprises a discharging device 8 that is configured to discharge deposit, during use of the filling apparatus 1a, from the inner volume 2a of the reusable reservoir 2. The discharging device 8 comprises a waste container 15 that is configured for storing deposit discharged from the inner volume 2a of the reusable reservoir 2. The waste container 15 is disposable, removable container that can be disposed together with the deposit discharged from the inner volume 2a of the reusable reservoir 2. The discharging device 8 is fluidly connected to the inner volume 2a of the reusable reservoir 2 via a first connection port 6. The first connection port 6 provides access to the inner volume 2a of the reusable reservoir 2 via an opening of the reusable reservoir 2.
The filling apparatus 1a further comprises a sterilization device 7 that is configured for sterilizing the inner volume 2a of the reusable reservoir 2. The sterilization device 7 comprises a radiation chamber 9 housing the reusable reservoir 2 when being received in a receiving portion 4 of the filling apparatus 1a. The receiving portion 4 holds the reusable reservoir 2 in place within the radiation chamber 9 during discharging, sterilizing and filling the inner volume 2a of the reusable reservoir 2. For sterilizing the inner volume 2a of the reusable reservoir 2, the sterilization device 7 further comprises a radiation source 12 that is configured to provide radiation within the radiation chamber 9 during use of the filling apparatus. The radiation provided by the radiation source 12 is selected so to achieve a sterility assurance level of 10−6. However, for protecting organisms close to the filling apparatus 1a against radiation provided by the radiation source 12, the radiation chamber 9 comprises a protective barrier 11. The protective barrier 11 hinders radiation from leaving the radiation chamber 9. The radiation chamber 9 comprises an access opening 10 that is configured to be opened and closed. When opened, the access opening 10 allows a reusable reservoir 2 to be inserted into the radiation chamber 9 and to be removed from the radiation chamber 9. When the access opening 10 is closed, the closed access opening 10 together with the protective barrier 11 hinders radiation leaving the radiation chamber 9.
After being sterilized, the inner volume 2a of the reusable reservoir 2 is filled with liquid medication. The filling apparatus 1a comprises a replaceable supply container 5 that is configured for containing the liquid medication. The supply container 5 is fluidly connected to the inner volume 2a of the reusable reservoir 2 via the first connection port 6. In order to either discharge deposit from the inner volume 2a from the reusable reservoir 2 or to fill liquid medication into the inner volume 2a from the reusable reservoir, the first connection port 6 is fluidly coupled to a valve 19. The valve 19 is configured to fluidly connect first connection port 6 alternately to either the supply container 5 or to the waste container 15.
Accordingly, the filling apparatus 1a is configured for carry out a method for filling a reusable reservoir 2 of a medical dispensing device 3 comprising the steps of discharging deposit from a reusable reservoir 2 by the discharging device 8 of the filling apparatus; sterilizing the inner volume 2a of the reusable reservoir 2 by providing radiation within the radiation chamber 9 by a radiation source 12 of a sterilization device 7 of the filling apparatus 1a; and filling the inner volume 2a of the reusable reservoir 2 by providing liquid medication from the supply container 5 of the filling apparatus 1a via the first connection port 6 of the filling apparatus 1a. Thus, the method is constituted to be executed by the filling apparatus 1a.
During use of the filling apparatus 1a, the plunger rod 2c is operatively coupled to the drive mechanism 20. The drive mechanism 20 is configured to actuate the plunger rod 2c which again is configured to move the plunger 2b within the inner volume 2a of the reusable reservoir 2. By moving the plunger 2b within the inner volume 2a of the reusable reservoir 2, the inner volume 2a is increased or decreased. By decreasing the inner volume 2a, deposit which is may present in the inner volume 2a will be discharged via the first connection port 6 into the waste container 15. Likewise, when moving the plunger 2b within the inner volume 2a of the reusable reservoir 2 so to increase the inner volume 2a liquid medication from the supply container 5 can be conveyed into the inner volume 2a of the reusable reservoir 2 via the first connection port 6.
The first connection port 6 and/or valve 19 according to this embodiment, further comprises an air-vent, the air vent is configured to fluidly connect the inner volume 2a of the reusable reservoir 2 to ambient air, thereby allowing to move the plunger 2b within the inner volume 2a without discharging deposit to the waste container 15 and without filling the inner volume 2a with liquid medication from the supply container 5. This design allows to provide an empty inner volume 2a of its maximum volume so that the radiation can pass through the inner volume 2a of the reservoir 2 along a direction perpendicular to the direction of movement of the plunger 2b without being substantially hindered by the plunger 2b and/or the plunger rod 2c.
Cleansing agent container 16 provides a cleansing agent for cleansing the inner volume 2a of the reusable reservoir 2. For example, a cleansing agent from the cleansing agent container 16 can be conveyed via the second connection port 21 into the inner volume 2a of the reusable reservoir 2 so to flush the inner volume 2a. In order to prevent an unintentional flow of liquid medication into the cleansing agent container and/or to prevent cleansing agent flowing from the cleansing agent container 16 into the supply container 5, a valve 19 is provided. Valve 19 is configured to alternately fluidly connect either the supply container 5 to the inner volume 2a of the reusable reservoir or the cleansing agent container 16 to the inner volume 2a of the reusable reservoir 2.
The discharging device 8 further comprises a heating module 17 that is configured for evaporating deposit in the inner volume 2a of the reusable reservoir 2. The evaporated deposit can than discharged from the reusable reservoir 2a of the reusable reservoir 2. Evaporated deposit can be discharged into the ambient air via an air-vent (not shown) or into the waste container 15.
Furthermore, the filling apparatus 1a comprises a charging device 22 that is configured for charging a rechargeable battery of a reusable reservoir 2 and/or a rechargeable battery of a medical dispensing device 3.
While exemplary embodiments have been disclosed hereinabove, the present invention is not limited to the disclosed embodiments. Instead, this application is intended to cover any variations, uses, or adaptations of this disclosure using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fall within the limits of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 22 201 703.0 | Oct 2022 | EP | regional |
This application is a continuation of International Application No. PCT/EP2023/078314, filed Oct. 12, 2023, which claims priority to European Application No. 22 201 703.0, filed Oct. 14, 2022, the entire disclosures of both of which are hereby incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/EP2023/078314 | Oct 2023 | WO |
| Child | 19176783 | US |
