EP3107821B1 - Vorrichtung zur verpackung und ausgabe eines produkts mit einer dosierdüse - Google Patents
Vorrichtung zur verpackung und ausgabe eines produkts mit einer dosierdüse Download PDFInfo
- Publication number
- EP3107821B1 EP3107821B1 EP15710545.3A EP15710545A EP3107821B1 EP 3107821 B1 EP3107821 B1 EP 3107821B1 EP 15710545 A EP15710545 A EP 15710545A EP 3107821 B1 EP3107821 B1 EP 3107821B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- actuating portion
- product
- layer
- rigid
- container
- 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.)
- Active
Links
- 238000004806 packaging method and process Methods 0.000 title claims description 9
- 239000000463 material Substances 0.000 claims description 23
- 238000001914 filtration Methods 0.000 claims description 10
- 239000004033 plastic Substances 0.000 claims description 8
- 229920003023 plastic Polymers 0.000 claims description 8
- 230000009471 action Effects 0.000 claims description 6
- 238000006073 displacement reaction Methods 0.000 claims description 5
- 230000008859 change Effects 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000013013 elastic material Substances 0.000 claims description 2
- 230000002787 reinforcement Effects 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 57
- 239000000047 product Substances 0.000 description 45
- 239000003570 air Substances 0.000 description 39
- 238000009826 distribution Methods 0.000 description 16
- 239000007788 liquid Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 230000000295 complement effect Effects 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000003466 welding Methods 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 235000021183 entrée Nutrition 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 241001415961 Gaviidae Species 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D47/00—Closures with filling and discharging, or with discharging, devices
- B65D47/04—Closures with discharging devices other than pumps
- B65D47/06—Closures with discharging devices other than pumps with pouring spouts or tubes; with discharge nozzles or passages
- B65D47/18—Closures with discharging devices other than pumps with pouring spouts or tubes; with discharge nozzles or passages for discharging drops; Droppers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D47/00—Closures with filling and discharging, or with discharging, devices
- B65D47/04—Closures with discharging devices other than pumps
- B65D47/20—Closures with discharging devices other than pumps comprising hand-operated members for controlling discharge
- B65D47/2018—Closures with discharging devices other than pumps comprising hand-operated members for controlling discharge comprising a valve or like element which is opened or closed by deformation of the container or closure
- B65D47/2056—Closures with discharging devices other than pumps comprising hand-operated members for controlling discharge comprising a valve or like element which is opened or closed by deformation of the container or closure lift valve type
Definitions
- the present invention relates to the technical field of packaging, and more particularly to that of packaging and dispensing a liquid or viscous product intended to be preserved in a sealed and sterile manner, without the addition of preservatives, and to be dispensed in the form of precise unit doses using a dispenser assembly.
- the invention more particularly relates to a device for packaging and dispensing a sterile product, and which comprises a container for containing the product to be dispensed with a measuring tip, of the type without air inlet whose container is provided.
- Such a device is known from the document WO 2010/089501 A1 .
- a relatively accurate dosage is obtained and the dosing unit ensures perfect bacteriological cleanliness at the end of the tip.
- the document FR 2941682 discloses a device for packaging and dispensing a product according to the preamble of claim 1.
- Conventional packaging devices are also known which make it possible to preserve and distribute a product in the form of portions or in any other form, while now sterile or safe from air for the duration of its use.
- These devices are used in particular in the pharmaceutical, cosmetic, and food fields, and for some more particularly in the ophthalmological field.
- a dispenser assembly which may be a flexible nozzle.
- This dispenser assembly is capable of dispensing portions of product but is designed to oppose any entry of air into the container.
- a filter is associated with the device and it can be in the bottom of the container or on the dispensing tip. This filter can be associated with an elastic valve located between the filter and the interior of the container to prevent contact between the product and the filter.
- the devices which comprise a flexible tip are not well adapted to deliver precise doses and / or the accuracy decreases as the device is manipulated.
- a first object of the invention is to allow the sterile maintenance of the product throughout the use of the device.
- a second object of the invention is to deliver very precise doses of the product in order to allow its use, in particular in the pharmaceutical field.
- a third goal is to combine the simplicity of the actuation for the user and durability of the tip.
- the invention aims to overcome the disadvantages of similar devices of the state of the art and to provide such a device that is very suitable for various requirements of practice.
- This arrangement of the dosing unit is advantageous in that the reinforcing layer can effectively prevent deformations of the first layer, which can modify the effective volume of product expelled from the dosing chamber, and that the connection of this reinforcement layer actively participates in the return of the actuating portion to its initial rest position when the device is no longer solicited.
- the device not only makes it possible to maintain the sterile product, to dispense precise doses of product by simple pressure on a flexible dispenser assembly integral with the container, but also to always generate the same pressure in the device as well as a greater return action. energetic only with the use of a single layer of flexible material, which facilitates the renewal of product in the metering chamber.
- the first layer is made of a first elastic material and the second layer comprises a second material that is preferentially more rigid than the first material (the second material being a rigid plastic material, such as for example polyethylene, polypropylene or similar plastic which is hard and therefore very flexible as soon as a threshold thickness of the order of a millimeter is exceeded).
- the portion rendered flexible is thus made of a material having a greater restoring force than the material of the flexible part.
- the second layer and the rigid portion are part of the same part obtained by plastic injection.
- This design of a part makes it possible to obtain a joint in a simple and economical way.
- the second layer, resiliently biased outwardly can advantageously exert traction on the first layer and provides a precise and regular filling of the metering chamber.
- the packaging and dispensing device comprises a rigid container 1, provided with a bottom 7 and a tubular side wall 19.
- An air intake assembly 20 is disposed in this bottom 7.
- this air intake assembly 20 is composed of a filter 8, a resilient valve 15 'or similar valve co-operating with a seat 6 and one or more orifices 9 and 18 for the passage of air.
- a rigid support piece S is sealed to the container 1 and a tip 3 provided with a flexible portion 25 is secured to the rigid support part S.
- the interior volume of the container 1 is therefore delimited by two rigid parts 1 and S, preferably of plastic molded separately, which are assembled in a sealed manner (with airtightness).
- the hole or holes 18 ' make it possible to communicate this interior volume, filled with product 11, with the inside of the mouthpiece 3.
- the rigid support piece S and the end piece 3 (which here has a generally tubular shape about a longitudinal axis X) can form a metering assembly 2 arranged in the extension of the container 1.
- the metering assembly 2 may be narrower than the container 1, having a maximum perimeter smaller than the perimeter of the side wall 19.
- a threaded zone 12 (visible on the Figures 3a-3b ) is optionally provided near the junction between the container 1 and a rigid portion 41 forming part of the tip 3, preferably on an outer surface of the rigid portion 41. This allows to assemble a protective cap (not shown ) which covers the dosing assembly 2 and typically extends the end 19a of the side wall 19.
- the metering assembly 2 may comprise a rigid guide element 5, which may form an integral part of the rigid support part S.
- the guide element 5 forms an axial projection, preferably in the form of rod, from a base 21 connected to the end 19a of the side wall 19.
- the metering assembly 2 comprises an actuating portion 35 which is formed here laterally in the endpiece 3 and which has an inner face 25a in contact with the product 11.
- This actuating portion 35 is movable and adapted to compress the product 11 present in a product dosing chamber 34, inside the dosing assembly 2.
- a valve 15 can be assembled directly or indirectly, so as to oppose any return to the inside of the container 1 of the product 11 contained in the metering chamber 34 when it is requested. by displacement of the actuating portion 35 (this stress being typically a pressure as for a push button) but allows the passage of the liquid 11 from the inside of the container 1 to the metering chamber 34 when the stress on the portion of actuation ceases and the actuating portion 35 elastically returns to its initial rest position, thereby creating a vacuum in the metering chamber 34.
- the figures 2b and 3b show the dosing assembly 2 when a pressure is exerted on the actuating portion 35 (relatively indeformable in the bearing zone because of its thickness) according to arrow A.
- the metering chamber 34 has a corresponding geometry with the inner contour of the actuating portion 35, so that the chamber 34 is completely emptied and the dose D of product 11 expelled from the device through the opening formed in the flexible material portion of the nozzle 3, around the end 5a of the guide element 5 here configured as a rod.
- the expulsion outside the device results from the circulation in the terminal section of the distribution channel 10, along the elastic mobile wall 24, which temporarily moves away from the end 5a under the effect of the pressure .
- the expulsion of the dose D is performed here parallel to the longitudinal axis X, the guide member 5 being rod-shaped to define this axis.
- the portion (30, 31, 36, 36 ', 39, 39') of flexible material is secured to the rigid material portion 41 by overmolding or by any other means such as welding or engagement force.
- This portion of flexible material, which extends to the free end 24a, is preferably longer than wide for good ergonomics of the dosing assembly 2. Its length is sufficient to allow easy support by the without being impeded by the wider part (forming a shoulder) of the rigid part 41. In the longitudinal direction, the length L of this part (30, 31, 36, 36 ', 39, 39') is greater than at least half the length of the support piece S.
- the layer 30 of the actuating portion 35 may have, in this longitudinal direction, a length L30 which is less than half the length L of the portion (30, 31, 36, 36 ') of flexible material (or more generally not more than two thirds of this length L). Preferably, this length L30 is greater than one third of the length L.
- the length L30 may correspond to a diameter when the actuating portion 35 has a substantially circular perimeter.
- the metering chamber 34 can be delimited by the inner face 25a, mobile, and three fixed surfaces, one of which corresponds to an abutment surface 37 formed by the guide member 5. It is understood that the use of one or more abutment surfaces 37, opposite the inner face 25a, makes it possible to limit the displacement of the actuating portion 35.
- the other two fixed surfaces are here formed by two faces 38 and 38 'of the end piece 3 (here defining two opposite edges of the fixed sub-part 31) which run along the guide element 5 and extend radially towards the end. outside from this guide member 5 to respective hinge portions 36, 36 ', elastic and thinned.
- These hinge portions 36, 36 ' may longitudinally surround at least a portion of the operable external surface of the layer 30 (herein defined as a thick portion).
- complementary hinge portions 39 and 39 ' may be provided at each axial end of the thick portion forming the layer 30.
- the complementary hinge portion 39' is thus located adjacent to the rigid portion 41 and may form an extension of hinge parts 36, 36 '.
- the inner face 25a, the abutment surface 37 and the faces 38, 38 ' extend longitudinally from an inlet end 34a of the chamber 34 to an outlet end.
- the inlet end 34a communicates with the hole or holes 18 'by a feed channel 10' situated between a portion of the rigid portion 41 and the guide element 5.
- This inlet end 34a is defined between the complementary hinge portion 39 'and guide member 5.
- the exit end is located on the free end 24a side.
- a supply channel 10 'and a distribution channel 10 are thus formed, on the one hand, and other of the metering chamber 34, in order to allow the transport of the product 11 between the hole or holes 18 'and the movable portion 24 of the valve 4 provided to define an outlet of the endpiece 3.
- the endpiece 3 may have a fixed subpart 31 made of the same material and of a block with the flexible part 25. As visible on the Figures 1, 2a-2b and 3a-3c this fixed sub-part 31 is contiguous and preferably fixedly attached (preferably by overmoulding) to the guide element 5, in the complementary angular sector of the sector where the metering chamber 34 extends.
- the Figures 2a-2b shows the metering chamber 34 in cross section, with a limitation of this chamber 34 to an angular portion (the angular sector being for example less than or equal to 120 °).
- the figure 2b illustrates a preferred option with a perfect contact of the inner face 25a against the abutment surface 37 by conforming to its shape and also hinge parts 36 and 36 'against the side edges or faces 38 and 38' due to the elongation elastic of these hinge portions 36 and 36 '.
- the flexible part 25 of the tip 3 for example made of silicone, similar flexible material or thermoplastic elastomer, axially extends the rigid portion 41, here of annular shape and has a thin and resilient portion or similar valve 4 cooperating with the end 5a of the guide member 5 for dispensing a dose D of product 11 when the device is biased.
- the actuating portion 35 comprises an inner layer or first layer 30 formed in the flexible portion 25, between the rigid portion 41 and the valve 4.
- the rigid portion 41 is, by way of non-limiting example, formed of a rigid material (in practice difficult to deform) such as a rigid plastic based on polyolefin, such as polyethylene or polypropylene. It extends here annularly around the longitudinal axis X.
- a rigid material in practice difficult to deform
- polyolefin such as polyethylene or polypropylene
- the piece forming the rigid portion 41 is extended locally by an axial projection which forms an outer layer or second layer 40 of the actuating portion 35.
- the second layer 40 is not reported on the first layer 30 of the portion of actuation 35 but is part of the rigid portion 41.
- the superposition of the two layers 30, 40 can increase the thickness of the actuating portion 35 (thick portion compared to the adjacent hinge portions 36, 36 ', 39, 39 ').
- the actuating portion 35 then sinks, here under the action of a lateral support along the arrow A (visible on the figures 2b and 3b ). Due to the inward displacement of the actuating portion 35, the fluid product (liquid or a low viscosity product or similar substance) present in the metering chamber 34 is compressed. Due to this inward movement, the movable portion of the nonreturn valve 15 is pushed against the base 21 to very effectively close the inlet passage or hole 18 'which communicates with the interior of the container 1 This allows the product 11 to leave the side of the free end 24a by deformation of the movable part 24 here flexible (which causes the opening of the valve 4), because of the thrust of the pressurized product which was enclosed in the chamber 34 of dosage.
- the inner face 25a is displaced to correspond exactly with the seat, here convex, formed by the abutment surface 37. More generally, the internal shape of the actuating portion 35 can correspond exactly to the geometry of the dosing chamber 34 when the dosing assembly 2 is biased.
- the elasticity of the flexible rendered portion 42 participates with the hinge portions 36, 36 ', 39 and 39' upon return of the actuating portion 35 to its initial rest position.
- the second rigid layer 40 makes it possible to reinforce the actuating portion 35. As a result, the product in the dosing chamber 34 can be effectively compressed and expelled, in the same way, after repeated use of the actuating portion 35 of the tip 3.
- the second layer 40 is formed by an axial projection which extends from a shoulder, here annular, of the rigid portion 41.
- the second layer 40 can oppose a direct contact of a finger of the user with the first layer 30.
- the second layer 40 may have a surface at least as large as that of the first layer 30 or form reliefs leaving spaces insufficiently large to allow a direct support on the first layer 30.
- the actuating portion 35 generates a depression inside the metering chamber 34.
- This depression causes the opening of the valve 15 which bends and comes off the support S which allows the passage of the liquid product 11 through the holes 18 'towards the inside of the metering chamber 34 which fills.
- the passage of the liquid 11 to the chamber 34 in turn causes a vacuum in the space 33 of the container 1 which does not contain product 11, which has the effect of lifting the valve 15 'from its seat 6 and thus to allow the inlet of the air from the outside to the inside of the container 1 through the air intake assembly 20 (for example via the holes 9, the filter 8 and the holes 18).
- the filter 8 having retained the external bacteria, the air entering the container 1 is sterile and the product 11 is not contaminated.
- This air intake ceases when the metering chamber 34 is completely filled and when the pressure balance between the inner space 33 and the outside of the container 1 is reached. The device is thus ready to be used again and to distribute an identical dose.
- the zone of joining between the first layer 30 and the second layer 40 can preferably be obtained by being secured by any means for fixing material at the interface between the two layers 30 and 40.
- the rigid projection forming the second layer 40 is only connected to the rigid portion 41 (and formed of a block with it) and the connection against the first layer 30 only results from the connection between the rigid portion 41 and the container 1.
- the rigid portion 41 differently, for example non-annularly and reported on a fixed part of the tip 3 (association by bonding, overmoulding or welding, or by any other means).
- the portion 42 made flexible is retained which is preferably formed in an intermediate zone of a rigid piece in one piece.
- the second layer 40 may be in the form of a push button, connected or not to the first layer 30 being contiguous on the outside thereof.
- the second layer 40, rigid, is then resting on a spring or equivalent elastic return member, for example assembled in a cavity of the rigid portion 41 (non-hinge option of the second layer 40).
- One or more abutment members are used in the connection between the second layer 40 and the rigid portion, knowing that this connection is configured to make the second layer 40 movable inwards and able to completely empty the chamber 34 .
- the device can be compact and is well suited for dispensing the same precise doses of liquid or slightly viscous product.
- the device is especially designed for pharmaceutical, cosmetic and ophthalmic applications.
- the actuating portion 35 is illustrated to be movable in a direction perpendicular to the longitudinal axis X, it is understood that the geometry of the tip 3 can be modified so that the actuating portion 35 formed with the two layers 30, 40, being mobile in a non-zero axial component direction or possibly in a substantially axial direction (in the latter case, the actuating portion 35 extends radially and is for example movable to an engaged position which corresponds to a support against the base portion 21).
- the metering chamber 34 can then be adjacent to the valve 15.
- the internal geometry of the actuating portion 35 preferably corresponds exactly to that of the metering chamber 34.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
- Closures For Containers (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Claims (11)
- Vorrichtung zur Verpackung und Ausgabe eines im Allgemeinen flüssigen Produkts, umfassend einen starren Behälter (1), der dazu bestimmt ist, das zu verpackende und auszugebende Produkt (11) zu enthalten, und eine Dosiereinheit (2), die dazu angepasst ist, eine vorbestimmte Dosis (D) des Produkts auszugeben, wobei die Dosiereinheit (2) Folgendes umfasst:- eine Spitze (3), die einen Betätigungsabschnitt (35) aufweist, der zwischen einer Ruheposition und einer Eingriffsposition mobil und dazu angepasst ist, die Ausgabe des Produkts zu betätigen;- ein starres, vorzugsweise stabförmiges Führungselement (5), das mindestens eine Anschlagfläche (37) aufweist, die dazu angepasst ist, die Bewegung des Betätigungsabschnitts (35) zu begrenzen und die Eingriffsposition zu definieren;- einen entlang des Führungselements (5) angeordneten Ausgabekanal (10);- eine erste Klappe (4), die es dem im Ausgabekanal (10) befindlichen Produkt erlaubt, aus der Spitze (3) auszutreten, wenn ein Druck auf den Betätigungsabschnitt (35) angewandt wird;- eine Produktdosierkammer (34), die mit dem Ausgabekanal (10) und einem Zufuhrkanal (10') in Verbindung steht und zwischen dem Führungselement (5) und dem Betätigungsabschnitt (35) begrenzt ist; wobei der Betätigungsabschnitt (35) eine in einem flexiblen Teil der Spitze (3) ausgebildete erste Schicht (30) aufweist,dadurch gekennzeichnet, dass der Betätigungsabschnitt (35) außerdem eine zweite Verstärkungsschicht (40) aufweist, welche die erste Schicht nach außen bedeckt, und dadurch, dass die Dosiereinheit (2) einen starren Abschnitt (41) umfasst, mit dem die zweite Schicht (40) des Betätigungsabschnitts (35) gelenkig und/oder mit einer Rückstellwirkung nach außerhalb der zweiten Schicht (40), wenn der auf den Betätigungsabschnitt (35) angewandte Druck aufgehoben wird, verbunden ist.
- Vorrichtung nach Anspruch 1, wobei die erste Schicht (30) durch ein erstes elastisches Material ausgeführt ist und die zweite Schicht (40) ein zweites Material umfasst, das starrer als das erste Material ist.
- Vorrichtung nach Anspruch 1 oder 2, wobei die zweite Schicht (40) und der starre Abschnitt (41) Teil eines selben Stücks sind, das durch Kunststoffspritzguss erhalten wird.
- Vorrichtung nach einem der Ansprüche 1 bis 3, wobei der flexible Teil (25) der Spitze (3) einen lokalen Verdünnungsbereich umfasst, der ein elastisches Gelenk ausbildet, wodurch jede der ersten und der zweiten Schicht (30, 40) des Betätigungsabschnitts (35) mit einem entsprechenden Gelenkbereich (36, 36', 39, 39', 42) verbunden ist.
- Vorrichtung nach einem der Ansprüche 1 bis 4, wobei sich die Spitze (3) in einer Längsrichtung bis zu einem freien Ende (24a) erstreckt und der Betätigungsabschnitt (35) radial nach innen beweglich ist, bis er an der Anschlagfläche (37) zur Anlage kommt, wobei der Betätigungsabschnitt (35) in Bezug auf das freie Ende (24a) in Längsrichtung versetzt ist, wobei sich der starre Abschnitt (41) vom freien Ende (24a) beabstandet erstreckt.
- Vorrichtung nach Anspruch 5, wobei die erste Klappe (4) eine Rückschlagklappe ist, die verhindert, dass Außenluft in den Ausgabekanal (10) eintritt, und die es dem Produkt erlaubt, aus der Spitze (3) auf der Seite des freien Endes (24a) auszutreten.
- Vorrichtung nach einem der Ansprüche 1 bis 6, wobei die Dosierkammer (34) aus dem Behälter (1) über den Zufuhrkanal (10') mit dem Produkt gespeist wird, wobei ein Übergang (18') einer zweiten Klappe (15) des Rückschlagtyps zugeordnet ist, um dem Rückstrom des Produkts (11) aus der Dosierkammer zum Behälterinneren entgegenzuwirken, wenn die Vorrichtung beaufschlagt wird, wobei die zweite Klappe (15) auf einem vom starren Abschnitt (41) getrennten starren Sockel (21) angebracht ist, wobei der starre Abschnitt (41) und der Sockel (21) miteinander verbunden und in Bezug auf den Behälter (1) fixiert sind.
- Vorrichtung nach einem der Ansprüche 1 bis 7, wobei die Spitze (3) um einen einstückig ausgebildeten mittleren axialen Sitz, der das Führungselement (5) einschließt, angeordnet ist, wobei die Dosierkammer (34) am Umfang des Führungselements (5) winkelbegrenzt ist, sodass die Dosierkammer (34) eine nicht ringförmige Gestaltung aufweist und sich nur auf der Seite des Betätigungsabschnitts (35) erstreckt
- Vorrichtung nach einem der Ansprüche 1 bis 8, wobei der Betätigungsabschnitt (35) einen Drucktaster definiert, wobei die erste Schicht (30) des Betätigungsabschnitts dazu gestaltet ist, die Anschlagfläche (37) in der Eingriffsposition gänzlich zu überdecken, um die Dosierkammer (34) in der Eingriffsposition des Betätigungsabschnitts vollständig zu leeren.
- Vorrichtung nach Anspruch 9, wobei sich die Spitze (3) ringartig um eine Längsachse (X) erstreckt und der in einer Seitenwand der Spitze (3) definierte Betätigungsabschnitt (35), dazu angeordnet ist, radial zur Längsachse (X) gedrückt zu werden.
- Vorrichtung nach einem der Ansprüche 1 bis 10, umfassend eine Luftaustausch- und Luftfiltereinheit, die es erlaubt, dass Außenluft nach der Ausgabe einer Dosis des Produkts (11) in den Behälter (1) strömen kann, wobei die Luftaustausch- und Luftfiltereinheit vorzugsweise ein Ventil (15') umfasst, das an einer Innenseite des Behälters (1) gegenüber der Dosiereinheit (2) montiert ist.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL15710545T PL3107821T3 (pl) | 2014-02-20 | 2015-02-11 | Urządzenie do kondycjonowania i dystrybucji produktu z wykorzystaniem końcówki dozującej |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/185,139 US9004317B2 (en) | 2004-07-20 | 2014-02-20 | Product packaging and dispensing device comprising a sterile filter bottle which is equipped with a nozzle |
FR1452900A FR3019529B1 (fr) | 2014-04-02 | 2014-04-02 | Dispositif de conditionnement et distribution d'un produit avec embout doseur |
PCT/FR2015/050330 WO2015124844A1 (fr) | 2014-02-20 | 2015-02-11 | Dispositif de conditionnement et distribution d'un produit avec embout doseur |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3107821A1 EP3107821A1 (de) | 2016-12-28 |
EP3107821B1 true EP3107821B1 (de) | 2018-01-24 |
Family
ID=52686395
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP15710545.3A Active EP3107821B1 (de) | 2014-02-20 | 2015-02-11 | Vorrichtung zur verpackung und ausgabe eines produkts mit einer dosierdüse |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP3107821B1 (de) |
JP (2) | JP6860349B2 (de) |
BR (1) | BR112016019273B1 (de) |
CA (1) | CA2938801C (de) |
DK (1) | DK3107821T3 (de) |
ES (1) | ES2663613T3 (de) |
HU (1) | HUE036660T2 (de) |
NO (1) | NO3107821T3 (de) |
PL (1) | PL3107821T3 (de) |
PT (1) | PT3107821T (de) |
RU (1) | RU2664345C2 (de) |
WO (1) | WO2015124844A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3134568A1 (fr) * | 2022-04-19 | 2023-10-20 | Promens Sa | Recipient ophtalmique du type sans air |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
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EP3320865B1 (de) | 2016-11-09 | 2020-08-19 | Medaxis Ag | Handstück zum aufstrahlen eines flüssigkeitsstrahls und einsetzteil für dieses handstück |
FR3080841B1 (fr) * | 2018-05-07 | 2020-04-10 | Jacques Pozzi | Dispositif de conditionnement et distribution d'un produit avec flacon et capot pressurisant |
GB201809627D0 (en) | 2018-06-12 | 2018-07-25 | Biorelevant Com Ltd | Methods for preparing buffer solutions suitable for in vitro drug dissolution testing, drug solubility testing and/or drug profiling |
FR3082835B1 (fr) * | 2018-06-21 | 2020-05-22 | Sivel | Dispositif de conditionnement et distribution d'un produit avec flacon et embout muni de joncs annulaires |
FR3102465B1 (fr) * | 2019-10-26 | 2022-06-03 | Sivel | Dispositif de conditionnement et distribution d'un produit avec flacon et capot d’amorcage |
US11958664B2 (en) | 2019-11-06 | 2024-04-16 | Horus Pharma | Dispensing device and assembly for packaging and dispensing product |
RU210059U1 (ru) * | 2021-12-21 | 2022-03-25 | Евгений Александрович Непокульчицкий | Устройство дозирования жидкости с многоразовым насосом |
Family Cites Families (8)
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JPH0223363U (de) * | 1988-07-28 | 1990-02-15 | ||
JP4463094B2 (ja) * | 2003-12-26 | 2010-05-12 | 参天製薬株式会社 | 底面フィルタ付液体収容容器 |
EP1940694B1 (de) * | 2005-09-20 | 2010-11-03 | 0736413 B.C. Ltd. | Vorrichtung zur abgabe von unter druck stehender steriler flüssigkeit |
FR2892397B1 (fr) * | 2005-10-26 | 2010-02-19 | Sivel | Dispositif de conditionnement et distribution d'un produit avec flacon muni d'une poche souple et d'un embout |
JP5472778B2 (ja) * | 2008-07-14 | 2014-04-16 | 隆 片山 | 搾出ノズルおよびレバー付容器 |
FR2941682B1 (fr) * | 2009-02-03 | 2016-03-11 | Sivel | Dispositif de conditionnement et distribution d'un produit propre ou sterile avec embout autonettoyant |
JP5783018B2 (ja) * | 2011-12-05 | 2015-09-24 | トヨタ自動車株式会社 | オイルパン |
FR2986703B1 (fr) * | 2012-02-09 | 2015-01-16 | Horus Pharma | Dispositif de conditionnement et de distribution d'un produit a usage ophtalmique |
-
2015
- 2015-02-11 CA CA2938801A patent/CA2938801C/fr active Active
- 2015-02-11 PT PT157105453T patent/PT3107821T/pt unknown
- 2015-02-11 EP EP15710545.3A patent/EP3107821B1/de active Active
- 2015-02-11 WO PCT/FR2015/050330 patent/WO2015124844A1/fr active Application Filing
- 2015-02-11 BR BR112016019273-7A patent/BR112016019273B1/pt active IP Right Grant
- 2015-02-11 RU RU2016137420A patent/RU2664345C2/ru active
- 2015-02-11 DK DK15710545.3T patent/DK3107821T3/en active
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- 2015-02-11 NO NO15710545A patent/NO3107821T3/no unknown
- 2015-02-11 ES ES15710545.3T patent/ES2663613T3/es active Active
- 2015-02-11 JP JP2016570191A patent/JP6860349B2/ja active Active
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3134568A1 (fr) * | 2022-04-19 | 2023-10-20 | Promens Sa | Recipient ophtalmique du type sans air |
WO2023203292A1 (fr) * | 2022-04-19 | 2023-10-26 | Promens Sa | Recipient ophtalmique du type sans air |
Also Published As
Publication number | Publication date |
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JP2017512160A (ja) | 2017-05-18 |
CA2938801A1 (fr) | 2015-08-27 |
ES2663613T3 (es) | 2018-04-16 |
DK3107821T3 (en) | 2018-04-16 |
PT3107821T (pt) | 2018-04-04 |
RU2016137420A (ru) | 2018-03-21 |
PL3107821T3 (pl) | 2018-07-31 |
NO3107821T3 (de) | 2018-06-23 |
WO2015124844A1 (fr) | 2015-08-27 |
RU2016137420A3 (de) | 2018-07-16 |
JP2020045173A (ja) | 2020-03-26 |
JP6860349B2 (ja) | 2021-04-14 |
CA2938801C (fr) | 2020-09-15 |
HUE036660T2 (hu) | 2018-07-30 |
RU2664345C2 (ru) | 2018-08-16 |
BR112016019273B1 (pt) | 2021-05-04 |
EP3107821A1 (de) | 2016-12-28 |
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