EP3081927A1 - Device for packaging loose medicament portions and method for the operation thereof - Google Patents
Device for packaging loose medicament portions and method for the operation thereof Download PDFInfo
- Publication number
- EP3081927A1 EP3081927A1 EP15163950.7A EP15163950A EP3081927A1 EP 3081927 A1 EP3081927 A1 EP 3081927A1 EP 15163950 A EP15163950 A EP 15163950A EP 3081927 A1 EP3081927 A1 EP 3081927A1
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- EP
- European Patent Office
- Prior art keywords
- blister
- packaging
- portions
- medication
- station
- 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.)
- Granted
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- 239000003814 drug Substances 0.000 title claims abstract description 78
- 238000004806 packaging method and process Methods 0.000 title claims abstract description 38
- 238000000034 method Methods 0.000 title claims description 15
- 229940079593 drug Drugs 0.000 claims abstract description 67
- 239000005022 packaging material Substances 0.000 claims abstract description 33
- 238000001514 detection method Methods 0.000 claims abstract description 23
- 230000003287 optical effect Effects 0.000 claims abstract description 20
- 230000002950 deficient Effects 0.000 claims abstract description 16
- 238000002372 labelling Methods 0.000 claims abstract description 12
- 238000007639 printing Methods 0.000 claims abstract description 11
- 238000011156 evaluation Methods 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 13
- 230000009897 systematic effect Effects 0.000 claims description 8
- 230000001960 triggered effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000011895 specific detection Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B9/00—Enclosing successive articles, or quantities of material, e.g. liquids or semiliquids, in flat, folded, or tubular webs of flexible sheet material; Subdividing filled flexible tubes to form packages
- B65B9/06—Enclosing successive articles, or quantities of material, in a longitudinally-folded web, or in a web folded into a tube about the articles or quantities of material placed upon it
- B65B9/08—Enclosing successive articles, or quantities of material, in a longitudinally-folded web, or in a web folded into a tube about the articles or quantities of material placed upon it in a web folded and sealed transversely to form pockets which are subsequently filled and then closed by sealing
- B65B9/087—Enclosing successive articles, or quantities of material, in a longitudinally-folded web, or in a web folded into a tube about the articles or quantities of material placed upon it in a web folded and sealed transversely to form pockets which are subsequently filled and then closed by sealing the web advancing continuously
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B57/00—Automatic control, checking, warning, or safety devices
- B65B57/10—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B57/00—Automatic control, checking, warning, or safety devices
- B65B57/10—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged
- B65B57/16—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged and operating to stop, or to control the speed of, the machine as a whole
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B61/00—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages
- B65B61/02—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages for perforating, scoring, slitting, or applying code or date marks on material prior to packaging
- B65B61/025—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages for perforating, scoring, slitting, or applying code or date marks on material prior to packaging for applying, e.g. printing, code or date marks on material prior to packaging
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B57/00—Automatic control, checking, warning, or safety devices
- B65B57/02—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of binding or wrapping material, containers, or packages
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B57/00—Automatic control, checking, warning, or safety devices
- B65B57/02—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of binding or wrapping material, containers, or packages
- B65B57/08—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of binding or wrapping material, containers, or packages and operating to stop, or to control the speed of, the machine as a whole
Definitions
- the present invention relates to a device for packaging individual medication portions.
- Corresponding devices are also referred to as blister machines and are known from the prior art. For example, this describes WO 2013/034504 A1 one in pharmacies and hospitals or, with appropriate dimensioning, even in blister centers usable Blisterautomaten, the drug compilations of several drug portions patient-individually according to the medically prescribed intake times compiles.
- the device packs order data corresponding drug compilations (which may comprise only a single portion of medication or a plurality of individual portions of medication) in bags formed of a packaging material sheet, so-called blister bags, these bags being a strand of blister bags (also referred to as "blister tubing") for further packaging Leave use.
- a blister bag regularly corresponds to a time of administration of a patient, ie contains all portions of medication that a patient must take at a given time of day.
- the order data itself may be, for example, data derived from recipes or the like.
- the known device for packaging individual medication portions comprises a plurality of storage and dispensing stations for medication portions, which cooperate with a plurality of circulating guide means which supply the medication portions also circulating collection means which supply the drug compositions to a packaging station in which the blister packs are formed and the each Medication portions when forming the blister pack are introduced into this. Due to the special construction of the device described above, a plurality of blister bags per hour is produced, and a corresponding identification of the blister bag is therefore of crucial importance.
- Labeling the blister pack after inserting the individual portions of medication is not practical, since the application of u.a. the contents of the blister bag characterizing data the medication portions are damaged.
- the application of the corresponding data is therefore carried out before the actual blistering, d. H. the formation of the blister bag and the introduction of the drug portions during molding.
- a labeling or printing device is arranged in front of the actual packaging site, which applies the data corresponding to the order data on the packaging material, which data uniquely identify the subsequently produced blister bag and reflect the content of each blister bag.
- the object is achieved by a device for packaging individual medication portions according to claim 1.
- the device according to the invention comprises a plurality of storage and dispensing stations for dispensing individual medication portions, at least one guiding and collecting arrangement for receiving the dispensed from the storage and dispensing stations medication portions and Forwarding said medication portions to a packaging station coupled to a controller which forms a string of connected blister bags from supplied packaging material and introduces the dispensed medication portions into the blister bags as the blister bags are formed.
- one or a plurality of guiding and collecting arrangements may be used. This may or may be made in one piece, but it is also envisaged that the guiding and collecting arrangements comprise separate guiding and collecting devices.
- the device further comprises a labeling or printing station coupled to the control device for applying data predetermined by the control device in a predetermined arrangement to the packaging material of each blister bag to be formed in the packaging station.
- the data to be applied are applied in a predetermined arrangement, ie on a predetermined section of the packaging material (and thus the subsequent blister bag), and may include, among other things, the date of manufacture of the blister bag, the exact content and possibly information on the deterioration of the contents of the blister bag.
- the manner of applying the data is not essential to the present invention.
- the data can be printed on the packaging material, but it is also conceivable that previously printed labels are adhered to the packaging material at the predetermined location. Furthermore, it is not essential what type of data is applied.
- the data it is possible for the data to be "readably" applied to a user, ie, for example, the name of the patient and the contents of the blister pack, ie the nature of the individual Medication portions, next to possibly other data, printed or glued.
- a barcode is applied, which at a later date may be supplemented or replaced by further data.
- the labeling or printing station may be part of the packaging station, ie both stations are combined in a component group.
- the labeling or printing station can be a separate component, which possibly improves the accessibility in the presence of a fault. Regardless of the nature of the application of the data and the nature of the data itself, it is essential that the data applied be readable by a user or machine at a later time.
- the device according to the invention further comprises an optical detection device coupled to the control device, which optically detects features of the individual blister bags of the strand, and an evaluation device coupled to the control device, which compares the features detected with a setpoint characteristic to a single blister bag.
- the evaluation device can be integrated in the control device. It is also conceivable that the function of both devices is performed by a common component, for example a computer.
- the detected features may, for example, merely be the location of the application of the data on the blister bag. If comparison with target features reveals that the data is applied in a location that is unsuitable for later machine acquisition of the data, this may indicate a bias in the application of the data (for example, if there are five or more blister bags in succession) have the same error), and the device is possibly stopped, the exact responses to the determination of a deviation between detected features and desired features depending on the nature and frequency of the deviations. So in the simplest case only determines whether the application of the data as such works properly.
- the optical detection means may also comprise such detection means which detect the number and size of the individual portions of medication placed in a blister bag. If the desired characteristics are derived from the order data to a blister bag, d. H. is held in the desired characteristics, how many portions of medication to be contained in a blister bag, a bag-specific deviation can be determined in this way, for example, if it is determined that the data are correctly applied to the blister bag, but due to a malfunction of the Device is not the correct number of individual medication portions is placed in a blister bag.
- the device according to the invention further comprises a storage station, in which the strand is stored in an orderly manner.
- order storage is meant that the strand of linked blister pack is rolled up, for example, or unfolded to a specific specification.
- the storage station can be arranged within the device, but it is also possible to improve the accessibility, an arrangement outside the actual device.
- the optical detection device is arranged between the packaging station and the storage station.
- blistering of blistered bags during blistering or production may result in systematic errors (misplacing the data, "unreadable” application of the data) and bag-related errors (incorrect number of medication portions, damaged portions of medication). If a systematic error occurs, it may be appropriate to stop the device so as to avoid producing a large number of defective blister bags. If there is only one bag-related error, however, it is regularly not indicated to stop the device.
- a marking device arranged between the optical detection device and the storage station and coupled to the control device, with which individual, identified as faulty Blister bag can be marked. For example, it is conceivable to simply provide a faulty blister bag with a striking color marking.
- the control device is first provided with order data, wherein these order data relate to medicament compilations, each with at least one medication portion.
- order data relate to medicament compilations, each with at least one medication portion.
- medication portions of a drug composition are dispensed and fed to the packaging station via at least one guiding and collecting arrangement.
- Data is applied to the packaging material from the labeling or printing station at predetermined application locations, and then a strand of connected blister packs is formed by the packaging station from the packaging material provided with the applied data, data being assigned to each blister bag, i. H. the blister bags are shaped so that are arranged on each previously applied data.
- the dispensed drug compositions are introduced into the blister bag.
- the strand of blister packs produced in this way is fed to an optical detection device, and with this, features of the blister packs are optically detected and the detected characteristics for a blister pack are compared with desired features.
- an optical detection device When determining a deviation between the detected characteristics and the target characteristics of a deviation associated reaction is triggered.
- the strand of blister packs leaving the optical detection means is stored, d. H. ordered stored (for example, on a roll).
- the optical detection device which may for example comprise a camera, detects predetermined features of the applied data. In the simplest case, for example, this may merely be the point of application of the data. If the data is correctly centered on the blister pouches (and thus on a corresponding location of the packaging material), the data will be determined with the optical detection device that the data is positioned too far "outwards" on the blister pouches Thus, in response to, for example, five consecutive defective blister bags, the device may be stopped. In this way, it is avoided that a large number of defective blister bag is generated.
- Which reaction is triggered depends on the type and frequency of the deviations determined. If, after a misprint of data on each other, for example, more than five blister packs printed without error occur, the operation of the device can be maintained despite the misprint. With the method according to the invention in its above-mentioned form, systematic errors in the application of the data can be detected and the device can be stopped if necessary, so that the production of a large number of defective blister bags, which could possibly be re-manufactured, can be avoided.
- the desired characteristics are derived from the order data, whereby the target characteristics and information about, for example Include number of individual portions of medication in a blister bag.
- the location of the data on the blister bag determined, for example, but also, for example, the number of individual medication portions is determined. If it is determined that although the application of the data on the blister bag is error-free, but a number of drug portions has been introduced into the blister, which does not match the desired characteristics, the blister bag can be marked as defective in such a bag-related deviation.
- the order data associated with the defective blister bag is marked as defective so as to facilitate, for example, later finding of the defective blister bag in the strand of the associated blister bag.
- the order data of a faulty blister bag for re-processing, so that it is possible without the intervention of a user, despite a first erroneous compilation to produce a blister bag whose drug composition corresponds to the order data.
- FIG. 1 shows a first embodiment of the device 1 according to the invention, wherein in this illustration only essential features are shown for the invention. Insignificant structural features, such as the outer wall, display and input means, etc. are omitted for the sake of simplicity.
- the device according to the invention comprises a support structure or frame 4 on which (m) a plurality of storage and dispensing stations 2 are detachably fastened, wherein a specific type of medicament portions can be arranged in each storage and dispensing station 2.
- a specific type of medicament portions can be arranged in each storage and dispensing station 2.
- two different portions of medication are arranged in each storage and dispensing station. In the case of such medication portions, which are frequently requested, however, it is also possible for the same portions of medication to be stored in several storage and dispensing stations 2.
- the storage and dispensing stations 2 are arranged in the embodiment shown in two opposite matrix structures 5 (of which only a matrix structure is shown), wherein the matrix structures 5 include two first horizontal conveyor belts 6a, 6b, to which guide means 7 are attached.
- the guide means are releasably secured by fasteners 8 which are part of the first two conveyor belts 6a, 6b.
- only a few guide devices 7 are shown; in practice, a guide device 7 is regularly fastened to each fastening element 8, so that the two first conveyor belts 6a, 6b are completely provided with conveying devices.
- the guide means are movable over the first conveyor belts along the storage and dispensing stations 2.
- a parallel processing of order data is made possible, since a guide device moves past each available portion of medication and thus with each guide device a medicament composition can be processed.
- a corresponding embodiment of the guide means is not essential to the present invention. It may, for example, only a single guide device be provided that can receive medication portions from all available storage and dispensing stations.
- the conveyor belts 6a, 6b are driven by drive rollers 12, which are coupled via a vertical shaft 10 with a motor 11. To prevent slippage of the first conveyor belts 6a, 6b in the drive rollers 12, these are advantageously provided with a surface contouring.
- the guide means 7 In order to be able to receive medication portions from all the storage and dispensing stations 2, the guide means 7 have a plurality of openings (not shown). In order to reduce the height of fall of the individual portions of medication in the guide means 7, they have in the embodiment shown a plurality of undercuts 14, which are each associated with a horizontal row of storage and dispensing stations.
- the device further comprises a second conveyor belt 15, which is arranged below the two first conveyor belts, and which likewise has a plurality of fastening elements 16.
- a collecting device 17 is fastened to the fastening elements, in which medicament compositions are temporarily stored intermediately prior to transfer to a packaging station 3.
- the second conveyor 15 is also coupled via a gear and the vertical shaft 10 to the motor 11, so that the guide means 7 and the collecting means 17 are moved at the same rotational speed.
- the device 1 does not extend the matrix of the storage and dispensing stations and the two first conveyor belts 6a, 6b over the entire length of the conveyor belt 15, but are, in view of the "length" of the device, kept shorter, so that at At a certain point within the device there is a separation between the guide means and the collecting means.
- the guiding and collecting devices (which together form the guiding and collecting arrangement) move in the area of the storage and storage devices in the embodiment shown Dispensing stations synchronously together, a separation takes place at the end of the matrix structure of the storage and dispensing stations.
- the device has several (or even only one) combined guiding and collecting arrangement, by means of which or which medicament compositions are guided to the packaging station 3.
- the collected drug compositions are supplied to the packaging station 3 by means of the plurality of movable collecting devices 17.
- the packaging station and the packaging station upstream components of the two embodiments of the device according to the invention will be described.
- the packaging station 3 is associated with a supply roll 32 with packaging material 34.
- the supply roll 32 itself is moved by a drive 33.
- the packaging material 34 is supplied to one by one with a (in FIG. 3 not visible) control device 80 coupled labeling or printing station 40 for applying predetermined by the controller data in a predetermined arrangement on the packaging material 34 out. How exactly the given data is applied to the packaging material depends on the particular embodiment. For example, it is conceivable that the data is printed on the packaging material 34, or that a label with the predetermined data is glued to the packaging material.
- the packaging material 34 leaves the labeling or printing station 40 with applied data 52, the data being applied to the packaging material 34 in such a way that the data are arranged at a likewise predetermined position on the blister bag for each blister bag to be subsequently formed.
- the packaging material provided with the data is supplied to a forming area of the packaging station 3, in which the Packaging material is folded centrally into a V-shape, in which the drug compositions can be introduced when opening the collection devices 17.
- the packaging material 34 is provided with a longitudinal and two transversely extending to the transport direction seals, which are formed by these seals self-contained blister. These are not separated after completion, but it forms a strand 50 with associated blister bags 51st
- two heating means 37 are provided, of which in FIG. 3 only one is shown. These two heating means press the two upper ends of the V-shaped folded packaging material together and weld them together.
- the transverse seals of the blister bag are made by two rotating heating means 39, the rotation of which is coordinated with each other. On the basis of the speed of movement of the packaging material 34 and the rotational speed of the heating means 39 can be precisely the length, and thus the capacity, control the blister bag.
- a corresponding packaging material 34 is to be selected.
- the packaging material must be adapted accordingly.
- the strand 50 is connected to the blister bags 51 from the packaging station 3 to a downstream of the packaging station 3 and guided to the control device 80 coupled optical detection device 40.
- This optical detection device comprises at least one detection means 41, which may be, for example, a camera. With the help of this detection means 41 features of the Capture device passing through blister bag detected. In the simplest case, for example, it is merely detected at which point of application of the blister bag the data previously applied with the labeling or printing device are arranged or whether (readable) data at all is arranged on the blister bags.
- the data is usually applied in a machine-readable form (for example, in the form of a bar code), it is essential that these are applied so that they are readable by a machine. For this purpose, it is necessary for the data to be arranged on the blister bag in a specific detection range of a machine reading out this data. If it is determined in the aforementioned comparison that this is not the case, the first blister bag in which this error was determined initially has a bag-specific error.
- a marking device 70 by means of which the blister bag recognized as defective is optically marked by means of at least one marking means 71, 72, for example by the bag is marked with a visually salient color.
- the operation of the device is stopped in response to the determined deviations in order to keep the number of defective blister bags low. After how many Deviations and what deviations exactly a stop of the device is initiated, depends on parameters that can be specified to the controller or the evaluation.
- the desired characteristics are derived from the order data, these also include “features" with regard to the drug composition contained in a blister bag.
- the target features include information about how many portions of medication comprises a drug compilation.
- the optical detection device optionally with an additional detection means 42, can determine how many portions of medicament are arranged in a blister bag, and this number is compared with the corresponding desired characteristic. If it is determined that there is a difference in the number of portions of medication, this blister pack is marked as defective.
- the blister bag can be optically marked for this, but it is also possible (additionally) to mark the order data as defective or to provide this order data for reworking, so as to ensure that the order data has also been processed after all order data have been processed whose first compilation may have failed.
- the strand 50 After the strand 50 has passed through the optical detection device, this is on a roller 62, which is driven by a motor 61, magazined.
- the strand may also be stored in an orderly folded manner, for example.
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Abstract
Die vorliegende Erfindung betrifft eine Vorrichtung zum Verpacken von einzelnen Medikamentenportionen in Blisterbeutel. Bei bekannten Vorrichtungen ist die Anzahl von fehlerhaften Blisterbeutels noch zu hoch. Die erfindungsgemäße Vorrichtung umfasst eine Mehrzahl von Speicher- und Abgabestationen (2), zumindest eine Führungs- und Sammelanordnung (7, 17) zum Aufnehmen und Weiterleiten der Medikamentenportionen an eine Verpackungsstation (3), welche aus Verpackungsmaterial (34) einen Strang (50) verbundener Blisterbeutel (51) formt, eine Etikettier- bzw. Druckstation (40) zum Aufbringen von Daten (52) auf das Verpackungsmaterial (34), eine optische Erfassungseinrichtung (40), welche Merkmale der einzelnen Blisterbeutel des Strangs optisch erfasst, eine Auswerteeinrichtung (90), welche die zu einem einzelnen Blisterbeutel erfassten Merkmale mit Soll-Merkmalen vergleicht, und eine Lagerstation (60), in welcher der Strang (50) der Blisterbeutel (51) geordnet gelagert wird, wobei die optische Erfassungseinrichtung (40) zwischen der Verpackungsstation (3) und der Lagerstation (60) angeordnet ist.The present invention relates to a device for packaging individual portions of medication in blisters. In known devices, the number of defective Blisterbeutels is still too high. The device according to the invention comprises a plurality of storage and dispensing stations (2), at least one guiding and collecting arrangement (7, 17) for receiving and forwarding the medicament portions to a packaging station (3), which consists of packaging material (34) a strand (50). connected blister bag (51) forms a labeling or printing station (40) for applying data (52) to the packaging material (34), an optical detection device (40) which optically detects features of the individual blister bags of the strand, an evaluation device ( 90), which compares the features detected in a single blister pack with target features, and a storage station (60) in which the strand (50) of the blister packs (51) is stored in an ordered manner, the optical detecting means (40) between the wrapping station (3) and the storage station (60) is arranged.
Description
Die vorliegende Erfindung betrifft eine Vorrichtung zum Verpacken von einzelnen Medikamentenportionen.The present invention relates to a device for packaging individual medication portions.
Entsprechende Vorrichtungen werden auch als Blisterautomaten bezeichnet und sind aus dem Stand der Technik bekannt. Beispielsweise beschreibt die
Die bekannte Vorrichtung zum Verpacken von einzelnen Medikamentenportionen umfasst eine Vielzahl von Speicher- und Abgabestationen für Medikamentenportionen, die mit einer Vielzahl von umlaufenden Führungseinrichtungen zusammenwirken, die die Medikamentenportionen ebenfalls umlaufenden Sammeleinrichtungen zuführen, welche die Medikamentenzusammenstellungen einer Verpackungsstation zuführen, in welcher die Blisterbeutel geformt und die einzelnen Medikamentenportionen beim Formen der Blisterbeutel in diese eingebracht werden. Aufgrund der speziellen Bauweise der oben beschriebenen Vorrichtung wird eine Vielzahl von Blisterbeuteln pro Stunde hergestellt, und eine entsprechende Kennzeichnung der Blisterbeutel ist daher von entscheidender Wichtigkeit.The known device for packaging individual medication portions comprises a plurality of storage and dispensing stations for medication portions, which cooperate with a plurality of circulating guide means which supply the medication portions also circulating collection means which supply the drug compositions to a packaging station in which the blister packs are formed and the each Medication portions when forming the blister pack are introduced into this. Due to the special construction of the device described above, a plurality of blister bags per hour is produced, and a corresponding identification of the blister bag is therefore of crucial importance.
Eine Kennzeichnung der Blisterbeutel nach Einbringen der einzelnen Medikamentenportionen ist nicht praktikabel, da beim Aufbringen von u.a. den Inhalt des Blisterbeutels kennzeichnenden Daten die Medikamentenportionen beschädigt werden. Die Aufbringung der entsprechenden Daten erfolgt daher vor der eigentlichen Verblisterung, d. h. der Formung des Blisterbeutels und der Einbringung der Medikamentenportionen während des Formens. Dazu ist vor der eigentlichen Verpackungsstelle eine Etikettier- oder Druckeinrichtung angeordnet, die den Auftragsdaten entsprechende Daten auf das Verpackungsmaterial aufbringt, wobei diese Daten den nachfolgend hergestellten Blisterbeutel eindeutig identifizieren und den Inhalt eines jeden Blisterbeutels wiederspiegeln.Labeling the blister pack after inserting the individual portions of medication is not practical, since the application of u.a. the contents of the blister bag characterizing data the medication portions are damaged. The application of the corresponding data is therefore carried out before the actual blistering, d. H. the formation of the blister bag and the introduction of the drug portions during molding. For this purpose, a labeling or printing device is arranged in front of the actual packaging site, which applies the data corresponding to the order data on the packaging material, which data uniquely identify the subsequently produced blister bag and reflect the content of each blister bag.
Tritt bei dem Aufbringen der Daten auf das Verpackungsmaterial ein (systematischer) Fehler auf (Druckbild verwischt bzw. unlesbar, versetzt, nur teilweise aufgebracht), kann dies aufgrund der Arbeitsgeschwindigkeit und der Art der aufgebrachten Daten (Barcode oder ähnliches) von einem Benutzer nicht oder nur sehr schwer festgestellt werden, so dass ggf. eine große Anzahl fehlerhafter Blisterbeutel hergestellt wird bevor der Fehler von einem Benutzer bemerkt wird. Ferner kann es vorkommen, dass ein (systematischer) Fehler im Hinblick auf die Herstellung der Blisterbeutel vorliegt, beispielsweise wenn eine häufig angeforderte Medikamentenportion nicht mehr vorrätig ist und dies von einer zugeordneten Speicher- und Abgabestationen nicht festgestellt wird.If a (systematic) error occurs during the application of the data to the packaging material (print image blurred or unreadable, offset, partially applied), this can not be done by a user due to the working speed and the type of data applied (barcode or similar) are found to be very difficult, so that if necessary, a large number of defective blister bag is made before the error is noticed by a user. Furthermore, it may happen that there is a (systematic) error with regard to the production of the blister pouches, for example if a frequently requested medication portion is no longer available and this is not detected by an associated storage and dispensing station.
Es ist daher Aufgabe der vorliegenden Erfindung, eine Vorrichtung zum Verpacken einzelner Medikamentenportionen zu schaffen, mit welcher die Anzahl fehlerhaft produzierter Blisterbeutel vermindert wird. Es ist ferner Aufgabe der vorliegenden Erfindung, ein entsprechendes Verfahren bereitzustellen.It is therefore an object of the present invention to provide a device for packaging individual medication portions, with which the number of incorrectly produced blister pack is reduced. It is a further object of the present invention to provide a corresponding method.
Die Aufgabe wird gelöst durch eine Vorrichtung zum Verpacken von einzelnen Medikamentenportionen gemäß Patentanspruch 1. Die erfindungsgemäße Vorrichtung umfasst eine Mehrzahl von Speicher- und Abgabestationen zum Abgeben einzelner Medikamentenportionen, zumindest eine Führungs- und Sammelanordnung zum Aufnehmen der von den Speicher- und Abgabestationen abgegebenen Medikamentenportionen und Weiterleiten dieser Medikamentenportionen an eine mit einer Steuereinrichtung gekoppelte Verpackungsstation, welche aus bereitgestelltem Verpackungsmaterial einen Strang verbundener Blisterbeutel formt und die abgegebenen Medikamentenportionen beim Formen der Blisterbeutel in die Blisterbeutel einbringt. In Abhängigkeit von der genauen Ausgestaltung der Vorrichtung kann eine oder eine Vielzahl von Führungs- und Sammelanordnungen verwendet werden. Diese kann bzw. können einteilig ausgeführt sein, es ist aber auch vorgesehen, dass die Führungs- und Sammelanordnungen getrennte Führungs- und Sammeleinrichtungen umfassen.The object is achieved by a device for packaging individual medication portions according to claim 1. The device according to the invention comprises a plurality of storage and dispensing stations for dispensing individual medication portions, at least one guiding and collecting arrangement for receiving the dispensed from the storage and dispensing stations medication portions and Forwarding said medication portions to a packaging station coupled to a controller which forms a string of connected blister bags from supplied packaging material and introduces the dispensed medication portions into the blister bags as the blister bags are formed. Depending on the exact configuration of the device, one or a plurality of guiding and collecting arrangements may be used. This may or may be made in one piece, but it is also envisaged that the guiding and collecting arrangements comprise separate guiding and collecting devices.
Die Vorrichtung umfasst ferner eine mit der Steuereinrichtung gekoppelte Etikettier- bzw. Druckstation zum Aufbringen von von der Steuereinrichtung vorgegebenen Daten in vorgegebener Anordnung auf das Verpackungsmaterial jedes in der Verpackungsstation zu formenden Blisterbeutels. Die aufzubringenden Daten werden in vorgegebener Anordnung, d. h. auf einem vorgegebenen Abschnitt des Verpackungsmaterials (und damit des späteren Blisterbeutels) aufgebracht, und können u. a. das Datum der Herstellung des Blisterbeutels, den genauen Inhalt und ggf. Informationen zum Verfall des Inhaltes des Blisterbeutels umfassen. Die Art der Aufbringung der Daten ist für die vorliegende Erfindung nicht wesentlich. So können die Daten beispielsweise auf das Verpackungsmaterial aufgedruckt werden, es ist aber auch denkbar, dass vorher bedruckte Etiketten an vorgegebener Stelle auf das Verpackungsmaterial aufgeklebt werden. Ferner ist es nicht wesentlich, welche Art von Daten aufgebracht wird. So ist es möglich, dass die Daten für einen Benutzer "lesbar" aufgebracht werden, d. h. dass beispielsweise der Name des Patienten und der Inhalt des Blisterbeutels, d. h. die Art der einzelnen Medikamentenportionen, neben ggf. weiteren Daten, aufgedruckt bzw. aufgeklebt werden. Es ist aber auch denkbar, dass lediglich ein Barcode aufgebracht wird, der zu einem späteren Zeitpunkt ggf. durch weitere Daten ergänzt oder ersetzt wird. In Abhängigkeit von der jeweiligen Ausführungsform kann die Etikettier- bzw. Druckstation Teil der Verpackungsstation sein, d.h. beide Stationen sind in einer Bauteilgruppe zusammengefasst. Alternativ kann die Etikettier- bzw. Druckstation ein separates Bauteil sein, was ggf. die Zugänglichkeit bei Vorliegen einer Störung verbessert. Unabhängig von der Art der Aufbringung der Daten und der Art der Daten selbst ist wesentlich, dass die aufgebrachten Daten zu einem späteren Zeitpunkt von einem Benutzer oder einer Maschine lesbar sind.The device further comprises a labeling or printing station coupled to the control device for applying data predetermined by the control device in a predetermined arrangement to the packaging material of each blister bag to be formed in the packaging station. The data to be applied are applied in a predetermined arrangement, ie on a predetermined section of the packaging material (and thus the subsequent blister bag), and may include, among other things, the date of manufacture of the blister bag, the exact content and possibly information on the deterioration of the contents of the blister bag. The manner of applying the data is not essential to the present invention. For example, the data can be printed on the packaging material, but it is also conceivable that previously printed labels are adhered to the packaging material at the predetermined location. Furthermore, it is not essential what type of data is applied. Thus, it is possible for the data to be "readably" applied to a user, ie, for example, the name of the patient and the contents of the blister pack, ie the nature of the individual Medication portions, next to possibly other data, printed or glued. However, it is also conceivable that only a barcode is applied, which at a later date may be supplemented or replaced by further data. Depending on the particular embodiment, the labeling or printing station may be part of the packaging station, ie both stations are combined in a component group. Alternatively, the labeling or printing station can be a separate component, which possibly improves the accessibility in the presence of a fault. Regardless of the nature of the application of the data and the nature of the data itself, it is essential that the data applied be readable by a user or machine at a later time.
Die erfindungsgemäße Vorrichtung umfasst ferner eine mit der Steuereinrichtung gekoppelte optische Erfassungseinrichtung, welche Merkmale der einzelnen Blisterbeutel des Strangs optisch erfasst, und eine mit der Steuereinrichtung gekoppelte Auswerteeinrichtung, welche die zu einem einzelnen Blisterbeutel erfassten Merkmale mit Soll-Merkmalen vergleicht. Die Auswerteeinrichtung kann in die Steuereinrichtung integriert sein. Es ist auch denkbar, dass die Funktion beider Einrichtungen von einem gemeinsamen Bauteil, beispielsweise einem Computer, ausgeführt wird.The device according to the invention further comprises an optical detection device coupled to the control device, which optically detects features of the individual blister bags of the strand, and an evaluation device coupled to the control device, which compares the features detected with a setpoint characteristic to a single blister bag. The evaluation device can be integrated in the control device. It is also conceivable that the function of both devices is performed by a common component, for example a computer.
Bei den erfassten Merkmalen kann es sich beispielsweise lediglich um den Ort der Aufbringung der Daten auf dem Blisterbeutel handeln. Wird bei einem Vergleich mit Soll-Merkmalen festgestellt, dass die Daten an einem Ort aufgebracht sind, der für eine spätere maschinelle Erfassung der Daten ungeeignet ist, kann dies einen systematischen Fehler bei der Aufbringung der Daten anzeigen (wenn beispielsweise fünf oder mehr Blisterbeutel in Folge den gleichen Fehler aufweisen), und die Vorrichtung wird ggf. angehalten, wobei die genauen Reaktionen auf das Ermitteln einer Abweichung zwischen erfassten Merkmalen und Soll-Merkmalen von der Art und Häufigkeit der Abweichungen abhängig ist. Im einfachsten Fall wird also lediglich ermittelt, ob die Aufbringung der Daten als solche einwandfrei funktioniert.The detected features may, for example, merely be the location of the application of the data on the blister bag. If comparison with target features reveals that the data is applied in a location that is unsuitable for later machine acquisition of the data, this may indicate a bias in the application of the data (for example, if there are five or more blister bags in succession) have the same error), and the device is possibly stopped, the exact responses to the determination of a deviation between detected features and desired features depending on the nature and frequency of the deviations. So in the simplest case only determines whether the application of the data as such works properly.
Die optische Erfassungseinrichtung kann jedoch auch solche Erfassungsmittel umfassen, die die Anzahl und Größe der in einem Blisterbeutel eingebrachten einzelnen Medikamentenportionen erfassen. Sofern die Soll-Merkmale aus den Auftragsdaten zu einem Blisterbeutel abgeleitet sind, d. h. in den Soll-Merkmalen festgehalten ist, wie viele Medikamentenportionen in einem Blisterbeutel enthalten sein sollen, kann auf diesem Wege auch eine beutelspezifische Abweichung ermittelt werden, beispielsweise wenn festgestellt wird, dass zwar die Daten korrekt auf den Blisterbeutel aufgebracht sind, jedoch aufgrund einer Fehlfunktion der Vorrichtung nicht die korrekte Anzahl an einzelnen Medikamentenportionen in einen Blisterbeutel eingebracht ist.However, the optical detection means may also comprise such detection means which detect the number and size of the individual portions of medication placed in a blister bag. If the desired characteristics are derived from the order data to a blister bag, d. H. is held in the desired characteristics, how many portions of medication to be contained in a blister bag, a bag-specific deviation can be determined in this way, for example, if it is determined that the data are correctly applied to the blister bag, but due to a malfunction of the Device is not the correct number of individual medication portions is placed in a blister bag.
Zum Lagern des hergestellten Stranges von verbundenen Blisterbeuteln umfasst die erfindungsgemäße Vorrichtung ferner eine Lagerstation, in welcher der Strang geordnet gelagert wird. Mit einer "geordneten" Lagerung ist gemeint, dass der Strang verbundener Blisterbeutel beispielsweise aufgerollt oder nach einer speziellen Vorgabe aufgefaltet wird. Die Lagerstation kann innerhalb der Vorrichtung angeordnet sein, möglich ist aber auch, zur Verbesserung der Zugänglichkeit, eine Anordnung außerhalb der eigentlichen Vorrichtung.For storing the manufactured strand of connected blister bags, the device according to the invention further comprises a storage station, in which the strand is stored in an orderly manner. By "ordered" storage is meant that the strand of linked blister pack is rolled up, for example, or unfolded to a specific specification. The storage station can be arranged within the device, but it is also possible to improve the accessibility, an arrangement outside the actual device.
Damit das Auftreten eines ggf. systematischen Fehlers erkannt werden kann, ist es erfindungswesentlich, dass die optische Erfassungseinrichtung zwischen der Verpackungsstation und der Lagerstation angeordnet ist.In order that the occurrence of a possibly systematic error can be detected, it is essential to the invention that the optical detection device is arranged between the packaging station and the storage station.
Wie bereits dargelegt, können bei der Verblisterung bzw. der Herstellung des Stranges verbundener Blisterbeutel systematische Fehler (Aufbringen der Daten bei falschem Ort, "unlesbares" Aufbringen der Daten) und beutelbezogene Fehler (falsche Anzahl an Medikamentenportionen, beschädigte Medikamentenportionen) auftreten. Bei Auftreten eines systematischen Fehlers kann es angezeigt sein, die Vorrichtung anzuhalten, so dass vermieden wird, dass eine große Anzahl fehlerhafter Blisterbeutel hergestellt werden. Bei Vorliegen lediglich eines beutelbezogenen Fehlers ist es regelmäßig jedoch nicht angezeigt, die Vorrichtung anzuhalten. Um es einem Benutzer zu erleichtern, einen fehlerhaften Blisterbeutel zu erkennen, ist es bei einer bevorzugten Ausführungsform der erfindungsgemäßen Vorrichtung vorgesehen, dass diese eine zwischen der optischen Erfassungseinrichtung und der Lagerstation angeordnete und mit der Steuereinrichtung gekoppelte Markiereinrichtung umfasst, mit welcher einzelne, als fehlerhaft erkannte Blisterbeutel markiert werden können. Beispielsweise ist es denkbar, einen fehlerhaften Blisterbeutel einfach mit einer auffälligen Farbmarkierung zu versehen.As already stated, blistering of blistered bags during blistering or production may result in systematic errors (misplacing the data, "unreadable" application of the data) and bag-related errors (incorrect number of medication portions, damaged portions of medication). If a systematic error occurs, it may be appropriate to stop the device so as to avoid producing a large number of defective blister bags. If there is only one bag-related error, however, it is regularly not indicated to stop the device. In order to make it easier for a user to recognize a faulty blister bag, in a preferred embodiment of the device according to the invention it is provided that it comprises a marking device arranged between the optical detection device and the storage station and coupled to the control device, with which individual, identified as faulty Blister bag can be marked. For example, it is conceivable to simply provide a faulty blister bag with a striking color marking.
Die Aufgabe wird ferner gelöst durch ein Verfahren gemäß Patentanspruch 3. Bei dem Verfahren zum Betreiben der Vorrichtung zum Verpacken von einzelnen Medikamentenportionen werden der Steuereinrichtung zunächst Auftragsdaten bereitgestellt, wobei diese Auftragsdaten Medikamentenzusammenstellungen mit jeweils zumindest einer Medikamentenportion betreffen. Von den Speicher- und Abgabestationen werden, basierend auf den Auftragsdaten, Medikamentenportionen einer Medikamentenzusammenstellung abgegeben und über zumindest eine Führungs- und Sammelanordnung der Verpackungsstation zugeführt. Von der Etikettier- bzw. Druckstation werden bei vorgegebenen Aufbringungsorten Daten auf das Verpackungsmaterial aufgebracht und anschließend wird von der Verpackungsstation aus dem bereitgestellten Verpackungsmaterial mit den aufgebrachten Daten ein Strang verbundener Blisterbeutel geformt, wobei jedem Blisterbeutel Daten zugeordnet werden, d. h. die Blisterbeutel derart geformt werden, dass auf jedem zuvor aufgebrachte Daten angeordnet sind. Während des Formens der Blisterbeutel werden die abgegebenen Medikamentenzusammenstellungen in die Blisterbeutel eingebracht.The object is further achieved by a method according to claim 3. In the method for operating the device for packaging individual medicament portions, the control device is first provided with order data, wherein these order data relate to medicament compilations, each with at least one medication portion. From the storage and dispensing stations, based on the order data, medication portions of a drug composition are dispensed and fed to the packaging station via at least one guiding and collecting arrangement. Data is applied to the packaging material from the labeling or printing station at predetermined application locations, and then a strand of connected blister packs is formed by the packaging station from the packaging material provided with the applied data, data being assigned to each blister bag, i. H. the blister bags are shaped so that are arranged on each previously applied data. During the molding of the blister bag, the dispensed drug compositions are introduced into the blister bag.
Der so hergestellte Strang verbundener Blisterbeutel wird einer optischen Erfassungseinrichtung zugeführt, und mit dieser werden Merkmale der Blisterbeutel optisch erfasst und die erfassten Merkmale für einen Blisterbeutel mit Soll-Merkmalen verglichen. Bei Ermittlung einer Abweichung zwischen den erfassten Merkmalen und den Soll-Merkmalen wird eine der Abweichung zugeordnete Reaktion ausgelöst.The strand of blister packs produced in this way is fed to an optical detection device, and with this, features of the blister packs are optically detected and the detected characteristics for a blister pack are compared with desired features. When determining a deviation between the detected characteristics and the target characteristics of a deviation associated reaction is triggered.
Schließlich wird der die optische Erfassungseinrichtung verlassende Strang der Blisterbeutel magaziniert, d. h. geordnet gelagert (beispielsweise auf einer Rolle).Finally, the strand of blister packs leaving the optical detection means is stored, d. H. ordered stored (for example, on a roll).
Mit Hilfe des erfindungsgemäßen Verfahrens lassen sich (systematische) Fehler beim Aufbringen der Daten auf das Verpackungsmaterial erkennen. Die optische Erfassungseinrichtung, welche beispielsweise eine Kamera umfassen kann, erfasst vorgegebene Merkmale der aufgebrachten Daten. Dabei kann es sich im einfachsten Fall beispielsweise lediglich um den Aufbringungsort der Daten handeln. Werden die Daten bei korrekter Funktion der Etikettier- bzw. Druckstation beispielsweise genau mittig auf die Blisterbeutel (und damit auf einen entsprechenden Ort des Verpackungsmaterials) aufgebracht und wird mit der optischen Erfassungseinrichtung ermittelt, dass die Daten zu weit "nach außen" auf den Blisterbeuteln angeordnet sind, so kann als Reaktion auf beispielsweise fünf aufeinanderfolgende fehlerhafte Blisterbeutel die Vorrichtung angehalten werden. Auf diese Weise wird vermieden, dass eine große Anzahl fehlerhafter Blisterbeutel erzeugt wird.With the aid of the method according to the invention, it is possible to detect (systematic) errors when applying the data to the packaging material. The optical detection device, which may for example comprise a camera, detects predetermined features of the applied data. In the simplest case, for example, this may merely be the point of application of the data. If the data is correctly centered on the blister pouches (and thus on a corresponding location of the packaging material), the data will be determined with the optical detection device that the data is positioned too far "outwards" on the blister pouches Thus, in response to, for example, five consecutive defective blister bags, the device may be stopped. In this way, it is avoided that a large number of defective blister bag is generated.
Welche Reaktion genau ausgelöst wird, hängt von der Art und der Frequenz der ermittelten Abweichungen ab. Folgen nach einem Fehldruck von Daten aufeinander wieder beispielsweise mehr als fünf fehlerfrei bedruckte Blisterbeutel, kann der Betrieb der Vorrichtung trotz des Fehldruckes aufrechterhalten werden. Mit dem erfindungsgemäßen Verfahren in seiner oben dargelegten Form können systematische Fehler bei der Aufbringung der Daten erkannt und die Vorrichtung ggf. angehalten werden, so dass die Herstellung einer großen Anzahl fehlerhafter Blisterbeutel, die ggf. neu herzustellen wären, vermieden werden kann.Which reaction is triggered depends on the type and frequency of the deviations determined. If, after a misprint of data on each other, for example, more than five blister packs printed without error occur, the operation of the device can be maintained despite the misprint. With the method according to the invention in its above-mentioned form, systematic errors in the application of the data can be detected and the device can be stopped if necessary, so that the production of a large number of defective blister bags, which could possibly be re-manufactured, can be avoided.
Um auch auf Fehler bei der Medikamentenzusammenstellung in einem Blisterbeutel reagieren zu können, ist es bei einer bevorzugten Ausführungsform des Verfahrens vorgesehen, dass die Soll-Merkmale aus den Auftragsdaten abgeleitet werden, wodurch die Soll-Merkmale auch Informationen über beispielsweise die Anzahl der einzelnen Medikamentenportionen in einem Blisterbeutel umfassen.In order to be able to react to errors in the drug composition in a blister bag, it is provided in a preferred embodiment of the method that the desired characteristics are derived from the order data, whereby the target characteristics and information about, for example Include number of individual portions of medication in a blister bag.
Bei dem optischen Erfassen der Merkmale eines Blisterbeutels wird dann nicht nur beispielsweise der Aufbringungsort der Daten auf dem Blisterbeutel ermittelt, sondern es wird beispielsweise auch die Anzahl der einzelnen Medikamentenportionen ermittelt. Wird dabei festgestellt, dass zwar die Aufbringung der Daten auf dem Blisterbeutel fehlerfrei ist, jedoch eine Anzahl von Medikamentenportionen in den Blisterbeutel eingebracht wurde, die nicht mit den Soll-Merkmalen übereinstimmt, kann der Blisterbeutel bei einer solchen beutelbezogenen Abweichung als fehlerhaft gekennzeichnet werden.In the optical detection of the characteristics of a blister bag, not only is the location of the data on the blister bag determined, for example, but also, for example, the number of individual medication portions is determined. If it is determined that although the application of the data on the blister bag is error-free, but a number of drug portions has been introduced into the blister, which does not match the desired characteristics, the blister bag can be marked as defective in such a bag-related deviation.
Bei einer bevorzugten Ausführungsform werden ferner die dem fehlerhaften Blisterbeutel zugeordneten Auftragsdaten als fehlerhaft gekennzeichnet, um so beispielsweise das spätere Auffinden des fehlerhaften Blisterbeutels in dem Strang der verbundenen Blisterbeutel zu vereinfachen. Alternativ oder zusätzlich werden die Auftragsdaten eines fehlerhaften Blisterbeutels zur erneuten Bearbeitung vorgesehen, so dass es ohne das Eingreifen eines Benutzers möglich ist, trotz einer ersten fehlerhaften Zusammenstellung einen Blisterbeutel herzustellen, dessen Medikamentenzusammenstellung den Auftragsdaten entspricht.In a preferred embodiment, furthermore, the order data associated with the defective blister bag is marked as defective so as to facilitate, for example, later finding of the defective blister bag in the strand of the associated blister bag. Alternatively or additionally, the order data of a faulty blister bag for re-processing, so that it is possible without the intervention of a user, despite a first erroneous compilation to produce a blister bag whose drug composition corresponds to the order data.
Im Nachfolgenden werden zwei bevorzugte Ausführungsformen der erfindungsgemäßen Vorrichtung sowie eine bevorzugte Ausführungsform des erfindungsgemäßen Verfahrens unter Bezugnahme auf die beigefügte Zeichnung beschrieben, in welcher
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Figur 1 eine schematische perspektivische Ansicht einer ersten Ausführungsform der erfindungsgemäßen Vorrichtung zeigt; -
eine schematische Seitenansicht einer zweiten Ausführungsform des erfindungsgemäßen Verfahrens zeigt; undFigur 2 -
Figur 3 eine Detailansicht des Abschnittes der Vorrichtung vor der eigentlichen Herstellung der Blisterbeutel zeigt.
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FIG. 1 shows a schematic perspective view of a first embodiment of the device according to the invention; -
FIG. 2 a schematic side view of a second embodiment of the method according to the invention; and -
FIG. 3 a detail view of the portion of the device before the actual production of the blister bag shows.
Die erfindungsgemäße Vorrichtung umfasst eine Stützstruktur bzw. Rahmen 4, an welcher(m) eine Mehrzahl von Speicher- und Abgabestationen 2 lösbar befestigt sind, wobei in jeder Speicher- und Abgabestation 2 eine bestimmte Art von Medikamentenportionen angeordnet werden können. Üblicherweise sind in jeder Speicher- und Abgabestation 2 unterschiedliche Medikamentenportionen angeordnet. Bei solchen Medikamentenportionen, die häufig angefragt werden, ist es jedoch auch möglich, dass in mehreren Speicher- und Abgabestationen 2 die gleichen Medikamentenportionen gespeichert sind.The device according to the invention comprises a support structure or
Die Speicher- und Abgabestationen 2 sind bei der gezeigten Ausführungsform in zwei gegenüberliegenden Matrixstrukturen 5 (von denen lediglich eine Matrixstruktur dargestellt ist) angeordnet, wobei die Matrixstrukturen 5 zwei erste horizontale Förderbänder 6a, 6b einschließen, an welchen Führungseinrichtungen 7 befestigt sind. Die Führungseinrichtungen sind lösbar über Befestigungselemente 8 befestigt, die Teil der beiden ersten Förderbänder 6a, 6b sind. Bei der gezeigten Ausführungsform sind lediglich einige Führungseinrichtungen 7 gezeigt, in der Praxis ist regelmäßig an jedem Befestigungselement 8 eine Führungseinrichtung 7 befestigt, so dass die beiden ersten Förderbänder 6a, 6b vollständig mit Fördereinrichtungen versehen sind.The storage and dispensing
Bei der gezeigten Ausführungsform sind die Führungseinrichtungen über die ersten Förderbänder entlang der Speicher- und Abgabestationen 2 bewegbar. Dadurch wird eine parallele Bearbeitung von Auftragsdaten ermöglicht, da sich eine Führungseinrichtung an jeder verfügbaren Medikamentenportion vorbeibewegt und somit mit jeder Führungseinrichtung eine Medikamentenzusammenstellung bearbeitet werden kann. Eine entsprechende Ausgestaltung der Führungseinrichtungen ist für die vorliegende Erfindung jedoch nicht wesentlich. Es kann beispielsweise auch lediglich eine einzige Führungseinrichtung bereitgestellt sein, die Medikamentenportionen aus sämtlichen verfügbaren Speicher- und Abgabestationen aufnehmen kann.In the embodiment shown, the guide means are movable over the first conveyor belts along the storage and dispensing
Die Förderbänder 6a, 6b werden über Antriebsrollen 12 angetrieben, welche über eine vertikale Welle 10 mit einem Motor 11 gekoppelt sind. Um bei den Antriebsrollen 12 ein Durchrutschen der ersten Förderbänder 6a, 6b zu vermeiden, sind diese vorteilhafterweise mit einer Oberflächenkonturierung versehen.The
Um Medikamentenportionen von sämtlichen Speicher- und Abgabestationen 2 aufnehmen zu können, weisen die Führungseinrichtungen 7 mehrere (nicht dargestellte) Öffnungen auf. Um die Fallhöhe der einzelnen Medikamentenportionen in den Führungseinrichtungen 7 zu verkleinern, weisen diese bei der gezeigten Ausführungsform eine Mehrzahl von Hinterschneidungen 14 auf, die jeweils einer horizontalen Reihe von Speicher- und Abgabestationen zugeordnet sind.In order to be able to receive medication portions from all the storage and dispensing
Die Vorrichtung umfasst ferner ein zweites Förderband 15, welches unterhalb der beiden ersten Förderbänder angeordnet ist, und welches ebenfalls eine Mehrzahl von Befestigungselementen 16 aufweist. An den Befestigungselementen ist jeweils eine Sammeleinrichtung 17 befestigt, in welcher Medikamentenzusammenstellungen vor der Übergabe dieser an eine Verpackungsstation 3 temporär zwischengelagert werden. Das zweite Förderband 15 ist ebenfalls über ein Zahnrad und die vertikale Welle 10 mit dem Motor 11 gekoppelt, so dass die Führungseinrichtungen 7 und die Sammeleinrichtungen 17 mit der gleichen Umlaufgeschwindigkeit bewegt werden. Wie dies insbesondere bei
Bei den in den
Der Verpackungsstation 3 ist eine Vorratsrolle 32 mit Verpackungsmaterial 34 zugeordnet. Die Vorratsrolle 32 selber wird durch einen Antrieb 33 bewegt. Das Verpackungsmaterial 34 wird zu einer bzw. durch eine mit einer (in
Das Verpackungsmaterial 34 verlässt die Etikettier- bzw. Druckstation 40 mit aufgebrachten Daten 52, wobei die Daten derart auf das Verpackungsmaterial 34 aufgebracht sind, dass bei jedem nachfolgend zu formenden Blisterbeutel die Daten bei einer ebenfalls vorgegebenen Position auf dem Blisterbeutel angeordnet sind. Mittels zweier Führungsrollen 35 wird das mit das Daten versehene Verpackungsmaterial einem Formgebungsbereich der Verpackungsstation 3 zugeführt, bei welchem das Verpackungsmaterial mittig zu einer V-Form gefaltet wird, in welche die Medikamentenzusammenstellungen bei Öffnen der Sammeleinrichtungen 17 eingebracht werden können.The
Das Verpackungsmaterial 34 wird mit einer längslaufenden und zwei quer zur Transportrichtung verlaufenden Dichtungen versehen, wobei durch diese Dichtungen in sich geschlossene Blisterbeutel entstehen. Diese werden nach Fertigstellung nicht voneinander getrennt, sondern es bildet sich ein Strang 50 mit verbundenen Blisterbeuteln 51.The
Zum Herstellen der Längsdichtung sind zwei Heizmittel 37 vorgesehen, von welchen in
Bei einer Abdichtung bzw. Herstellung der Blisterbeutel mit Heizmitteln ist ein entsprechendes Verpackungsmaterial 34 zu wählen. Bei alternativen Ausführungsbeispielen ist es möglich, die einzelnen Blisterbeutel auf andere Art und Weise herzustellen, wobei dann das Verpackungsmaterial entsprechend anzupassen ist. So ist es beispielsweise auch möglich, beim Herstellen der Blisterbeutel ein Dicht- bzw. Klebematerial aufzubringen, über dessen Haftwirkung der Blisterbeutel erzeugt wird.In a sealing or production of the blister bag with heating means, a corresponding
Wie dies in den
Diese "Merkmale" eines die optische Erfassungseinrichtung durchlaufenden Blisterbeutel werden von einer mit der Steuereinrichtung 80 gekoppelten Auswerteeinrichtung 90 (die beiden vorgenannten Einrichtungen sind lediglich in
Da die Daten üblicherweise in einer maschinenlesbaren Form aufgebracht sind (beispielswiese in Form eines Barcodes), ist es wesentlich, dass diese derart aufgebracht sind, dass sie von einer Maschine lesbar sind. Dazu ist es erforderlich, dass die Daten in einem bestimmten Erfassungsbereich einer diese Daten auslesenden Maschine auf dem Blisterbeutel angeordnet sind. Wird nun bei dem vorgenannten Vergleich ermittelt, dass dies nicht der Fall ist, liegt bei dem ersten Blisterbeutel, bei dem dieser Fehler ermittelt wurde, zunächst ein beutelspezifischer Fehler vor. Um dies bei dem Blisterbeutel auch optisch sichtbar zu machen, umfasst die in
Wird bei dem bzw. den dem ersten fehlerhaften Blisterbeutel nachfolgenden Blisterbeuteln der gleiche bzw. ähnliche Fehler festgestellt, wird als Reaktion auf die ermittelten Abweichungen der Betrieb der Vorrichtung angehalten, um die Anzahl fehlerhafter Blisterbeutel gering zu halten. Nach wie vielen Abweichungen und welchen Abweichungen genau ein Anhalten der Vorrichtung eingeleitet wird, hängt von Parametern ab, die der Steuereinrichtung bzw. der Auswerteeinrichtung vorgegeben werden können.If the same or similar errors are detected in the blister bag or blisters following the first defective blister bag, the operation of the device is stopped in response to the determined deviations in order to keep the number of defective blister bags low. After how many Deviations and what deviations exactly a stop of the device is initiated, depends on parameters that can be specified to the controller or the evaluation.
Für den Fall, dass die Soll-Merkmale von den Auftragsdaten abgeleitet sind, umfassen diese auch "Merkmale" im Hinblick auf die in einem Blisterbeutel befindliche Medikamentenzusammenstellung. Beispielsweise enthalten die Soll-Merkmale Angaben darüber, wie viele Medikamentenportionen eine Arzneimittelzusammenstellung umfasst. In einem solchen Fall kann bzw. wird mit der optischen Erfassungseinrichtung, ggf. mit einem zusätzlichen Erfassungsmittel 42, ermittelt, wie viele Medikamentenportionen in einem Blisterbeutel angeordnet sind und diese Anzahl wird mit dem entsprechenden Soll-Merkmal verglichen. Wird festgestellt, dass im Hinblick auf die Anzahl der Medikamentenportionen eine Abweichung vorliegt, wird dieser Blisterbeutel als fehlerhaft markiert. Wie bereits dargelegt, kann dazu der Blisterbeutel optisch markiert werden, es ist aber auch (zusätzlich) möglich, die Auftragsdaten als fehlerhaft zu markieren oder diese Auftragsdaten zur erneuten Bearbeitung vorzusehen, so dass gewährleistet ist, dass nach Durchlauf sämtlicher Auftragsdaten auch die Auftragsdaten verarbeitet wurden, bei deren erster Zusammenstellung ggf. ein Fehler aufgetreten ist.In the case that the desired characteristics are derived from the order data, these also include "features" with regard to the drug composition contained in a blister bag. For example, the target features include information about how many portions of medication comprises a drug compilation. In such a case, the optical detection device, optionally with an additional detection means 42, can determine how many portions of medicament are arranged in a blister bag, and this number is compared with the corresponding desired characteristic. If it is determined that there is a difference in the number of portions of medication, this blister pack is marked as defective. As already stated, the blister bag can be optically marked for this, but it is also possible (additionally) to mark the order data as defective or to provide this order data for reworking, so as to ensure that the order data has also been processed after all order data have been processed whose first compilation may have failed.
Nachdem der Strang 50 die optische Erfassungseinrichtung durchlaufen hat, wird dieser auf einer Rolle 62, welche von einem Motor 61 angetrieben ist, magaziniert. Bei alternativen Ausführungsformen kann der Strang auch beispielsweise geordnet gefaltet gelagert werden.After the
Claims (8)
eine Mehrzahl von Speicher- und Abgabestationen (2) zum Abgeben einzelner Medikamentenportionen,
zumindest eine Führungs- und Sammelanordnung (7, 17) zum Aufnehmen der von den Speicher- und Abgabestationen (2) abgegebenen Medikamentenportionen und Weiterleiten dieser Medikamentenportionen an
eine mit einer Steuereinrichtung (80) gekoppelte Verpackungsstation (3), welche aus bereitgestelltem Verpackungsmaterial (34) einen Strang (50) verbundener Blisterbeutel (51) formt und die abgegebenen Medikamentenportionen beim Formen der Blisterbeutel in die Blisterbeutel einbringt,
eine mit der Steuereinrichtung (80) gekoppelte Etikettier- bzw. Druckstation (40) zum Aufbringen von von der Steuereinrichtung (80) vorgebebenen Daten (52) in vorgegebener Anordnung auf das Verpackungsmaterial (34),
eine mit der Steuereinrichtung (80) gekoppelte optische Erfassungseinrichtung (40), welche Merkmale der einzelnen Blisterbeutel des Strangs optisch erfasst,
eine mit der Steuereinrichtung (80) gekoppelte Auswerteeinrichtung (90), welche die zu einem einzelnen Blisterbeutel erfassten Merkmale mit Soll-Merkmalen vergleicht, und
eine Lagerstation (60), in welcher der Strang (50) der Blisterbeutel (51) geordnet gelagert wird,
wobei die optische Erfassungseinrichtung (40) zwischen der Verpackungsstation (3) und der Lagerstation (60) angeordnet ist.Device (1) for packaging individual portions of medicament, comprising
a plurality of storage and dispensing stations (2) for dispensing individual portions of medication,
at least one guiding and collecting arrangement (7, 17) for receiving the portions of medication dispensed by the storage and dispensing stations (2) and forwarding these portions of medication
a packaging station (3) coupled to a control device (80) which forms a strand (50) of connected blister bags (51) from supplied packaging material (34) and inserts the dispensed medication portions into the blisters when the blister bags are formed,
a labeling or printing station (40) coupled to the control device (80) for applying data (52) provided by the control device (80) in a predetermined arrangement to the packaging material (34),
an optical detection device (40) coupled to the control device (80) which optically detects features of the individual blister bags of the strand,
an evaluation device (90) which is coupled to the control device (80) and which compares the features acquired with a setpoint characteristic to a single blister bag, and
a storage station (60) in which the strand (50) of the blister bag (51) is stored in an ordered manner,
wherein the optical detection means (40) is disposed between the packaging station (3) and the storage station (60).
der Steuereinrichtung (80) Auftragsdaten bereitgestellt werden, wobei die Auftragsdaten Medikamentenzusammenstellungen mit jeweils zumindest einer Medikamentenportion betreffen,
von den Speicher- und Abgabestationen (2), basierend auf den Auftragsdaten, Medikamentenportionen einer Medikamentenzusammenstellung abgegeben werden,
die Medikamentenzusammenstellungen der Verpackungsstation (3) zugeführt werden,
von der Etikettier- bzw. Druckstation (70) Daten (52) auf das Verpackungsmaterial (34) bei vorgegebenen Aufbringungsorten aufgebracht werden,
von der Verpackungsstation (3) aus dem bereitgestellten Verpackungsmaterial (34) mit den aufgebrachten Daten ein Strang (50) verbundener Blisterbeutel (51) geformt wird, wobei jedem Blisterbeutel Daten zugeordnet werden, und die abgegebenen Medikamentenzusammenstellungen während des Formens der Blisterbeutel in die Blisterbeutel eingebracht werden,
der Strang (50) einer optischen Erfassungseinrichtung (40) zugeführt wird und Merkmale eines Blisterbeutel optisch erfasst werden,
die erfassten Merkmale für einen Blisterbeutel mit Soll-Merkmalen verglichen werden und bei Ermittlung einer Abweichung zwischen den erfassten Merkmalen und den Soll-Merkmalen eine der Abweichung zugeordnete Reaktion ausgelöst wird, und
der Strang der Blisterbeutel magaziniert wird.A method of operating the device for packaging individual medication portions according to any one of claims 1-2, wherein
order data are provided to the control device (80), the order data relating to drug compilations each comprising at least one portion of medication,
from the storage and dispensing stations (2), drug portions of a drug composition are dispensed based on the order data;
the drug compositions are supplied to the packaging station (3),
from the labeling or printing station (70) data (52) are applied to the packaging material (34) at predetermined application locations,
from the packaging station (3) from the provided packaging material (34) with the data applied, a strand (50) of blister packs (51) is formed, each data being associated with each blister pack, and the dispensed drug compilations are introduced into the blister packs during blister bag forming become,
the strand (50) is fed to an optical detection device (40) and features of a blister bag are optically detected,
the detected characteristics for a blister bag are compared with desired characteristics and, when a deviation between the detected characteristics and the desired characteristics is determined, a response associated with the deviation is triggered, and
the strand of blister bag is magaziniert.
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP15163950.7A EP3081927B1 (en) | 2015-04-17 | 2015-04-17 | Device for packaging loose medicament portions and method for the operation thereof |
PT151639507T PT3081927T (en) | 2015-04-17 | 2015-04-17 | Device for packaging loose medicament portions and method for the operation thereof |
ES15163950.7T ES2665279T3 (en) | 2015-04-17 | 2015-04-17 | Device for packaging individual portions of medicines and procedure for their operation |
DK15163950.7T DK3081927T3 (en) | 2015-04-17 | 2015-04-17 | DEVICE FOR PACKING OF INDIVIDUAL MEDICINE PORTIONS AND PROCEDURES FOR OPERATING THEREOF |
CA2983375A CA2983375C (en) | 2015-04-17 | 2016-04-14 | Apparatus for packaging individual medication doses and method for its operation |
AU2016247382A AU2016247382B2 (en) | 2015-04-17 | 2016-04-14 | Device for packaging individual medicament portions, and method for operating said device |
CN201680022426.4A CN107531352B (en) | 2015-04-17 | 2016-04-14 | Equipment and operating method for packing list part drug dose |
PCT/EP2016/058163 WO2016166187A1 (en) | 2015-04-17 | 2016-04-14 | Device for packaging individual medicament portions, and method for operating said device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP15163950.7A EP3081927B1 (en) | 2015-04-17 | 2015-04-17 | Device for packaging loose medicament portions and method for the operation thereof |
Publications (2)
Publication Number | Publication Date |
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EP3081927A1 true EP3081927A1 (en) | 2016-10-19 |
EP3081927B1 EP3081927B1 (en) | 2018-01-31 |
Family
ID=52991515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP15163950.7A Active EP3081927B1 (en) | 2015-04-17 | 2015-04-17 | Device for packaging loose medicament portions and method for the operation thereof |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP3081927B1 (en) |
CN (1) | CN107531352B (en) |
AU (1) | AU2016247382B2 (en) |
CA (1) | CA2983375C (en) |
DK (1) | DK3081927T3 (en) |
ES (1) | ES2665279T3 (en) |
PT (1) | PT3081927T (en) |
WO (1) | WO2016166187A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2020057807A1 (en) * | 2018-09-21 | 2020-03-26 | Gebr. Willach Gmbh | Tablet portioning device |
CN114486923A (en) * | 2022-03-14 | 2022-05-13 | 南通理工学院 | Online continuous detection device and method for surface defects of shaft parts based on compressed sensing |
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EP3767531A1 (en) * | 2019-07-19 | 2021-01-20 | Becton Dickinson Rowa Germany GmbH | Method for measuring and verifying drug portions and computer program products |
US11673700B2 (en) | 2021-06-22 | 2023-06-13 | Vmi Holland B.V. | Device and methods for packaging medicaments with fault detection |
US11273103B1 (en) | 2021-06-22 | 2022-03-15 | Vmi Holland B.V. | Method, computer program product and dispensing device for dispensing discrete medicaments |
US11498761B1 (en) | 2021-06-22 | 2022-11-15 | Vmi Holland B.V. | Method for dispensing discrete medicaments, a test station for testing a feeder unit, and a method for determining a fill level of a feeder unit |
US12036185B2 (en) | 2021-07-19 | 2024-07-16 | Optum, Inc. | System and method to count pills |
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- 2015-04-17 ES ES15163950.7T patent/ES2665279T3/en active Active
- 2015-04-17 DK DK15163950.7T patent/DK3081927T3/en active
- 2015-04-17 EP EP15163950.7A patent/EP3081927B1/en active Active
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2016
- 2016-04-14 AU AU2016247382A patent/AU2016247382B2/en active Active
- 2016-04-14 CN CN201680022426.4A patent/CN107531352B/en active Active
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CN114486923A (en) * | 2022-03-14 | 2022-05-13 | 南通理工学院 | Online continuous detection device and method for surface defects of shaft parts based on compressed sensing |
Also Published As
Publication number | Publication date |
---|---|
PT3081927T (en) | 2018-04-24 |
ES2665279T3 (en) | 2018-04-25 |
CN107531352B (en) | 2019-10-29 |
AU2016247382A1 (en) | 2017-09-28 |
WO2016166187A1 (en) | 2016-10-20 |
CA2983375A1 (en) | 2016-10-20 |
CA2983375C (en) | 2023-05-09 |
AU2016247382B2 (en) | 2020-12-03 |
DK3081927T3 (en) | 2018-04-30 |
CN107531352A (en) | 2018-01-02 |
EP3081927B1 (en) | 2018-01-31 |
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