A zipper (100) includes a male closure element (101) and a female closure element (102). The male closure element includes a base member (103), one or more male interlocking members (201,203) extending distally from a first side of the base member, and a plurality of guide posts (105,107) extending from a second side of the base member. The female closure element includes a base member (104), one or more female interlocking members (202,204) extending distally from a first side of the base member, and a plurality of guide posts (106,108) extending from a second side of the base member.

A zipper (100) includes a male closure element (101) and a female closure element (102). The male closure element includes a base member (103), one or more male interlocking members (201,203) extending distally from a first side of the base member, and a plurality of guide posts (105,107) extending from a second side of the base member. The female closure element includes a base member (104), one or more female interlocking members (202,204) extending distally from a first side of the base member, and a plurality of guide posts (106,108) extending from a second side of the base member.

An actuator system for fabricating a cavity within thermoplastic material includes a plurality of actuators arranged in an array. When dimensions of an item are determined, the actuator system may be programmed with data regarding such dimensions to fabricate a cavity for the item. A subset of the actuators, and distances by which each of the actuators is to be extended, may be selected based on dimensions of the item, in order to fabricate a cavity within the thermoplastic material that may accommodate the item therein. Additionally, the actuators and the distances may be selected based on intrinsic or extrinsic data regarding the item, and a cavity fabricated within the thermoplastic material may include one or more buffer zones or protective regions that are specifically formed with respect to aspects of the item.

An actuator system for fabricating a cavity within thermoplastic material includes a plurality of actuators arranged in an array. When dimensions of an item are determined, the actuator system may be programmed with data regarding such dimensions to fabricate a cavity for the item. A subset of the actuators, and distances by which each of the actuators is to be extended, may be selected based on dimensions of the item, in order to fabricate a cavity within the thermoplastic material that may accommodate the item therein. Additionally, the actuators and the distances may be selected based on intrinsic or extrinsic data regarding the item, and a cavity fabricated within the thermoplastic material may include one or more buffer zones or protective regions that are specifically formed with respect to aspects of the item.

An installation for producing a support for a product in a unitary dose including a supply member of a material web, a cutting apparatus to obtain a support card having a main portion, in which there is formed a main opening, and a foldable flap, in which there is formed a secondary opening. The installation further includes movement members for receiving the packaging of a product in a unitary dose so that a portion projects from the main opening and a peripheral edge is supported on the main portion of the card. The installation also includes folding members for folding the flap so as to enclose a portion of the peripheral edge between the flap and the main portion of the card. The installation also includes a fixing apparatus for fixing the flap to the main portion of the card.

The method for producing blister packs for medicinal products comprises the steps of forming blister pockets in a bottom film, wherein each blister pocket has an at least two-level shape with a first recess and a second, lower recess, filling the second recesses of the blister pockets with the medicinal products, placing a strip of active material in the first recess of each blister pocket above the medicinal product, wherein the strip of active material rests on at least one support surface of the first recess next to the second recess, sealing a lidding film to webs of the bottom film arranged around the blister pockets and simultaneously to the strips of active material, thus forming a sealed blister web, and stamping out individual blister packs from the blister web.

The method for producing blister packs for medicinal products comprises the steps of forming blister pockets in a bottom film, wherein each blister pocket has an at least two-level shape with a first recess and a second, lower recess, filling the second recesses of the blister pockets with the medicinal products, placing a strip of active material in the first recess of each blister pocket above the medicinal product, wherein the strip of active material rests on at least one support surface of the first recess next to the second recess, sealing a lidding film to webs of the bottom film arranged around the blister pockets and simultaneously to the strips of active material, thus forming a sealed blister web, and stamping out individual blister packs from the blister web.

A package has a plurality of seamless compartments coupled together. A different one of the plurality compartments each includes a different respective one of a plurality of respective void spaces and a different respective one of a plurality of respective void space delimiting surfaces. A different one of a plurality of fill entries each forms a fluent entry into a different respective compartment's void space. At least one fill entry of said plurality is in an elastomeric portion of said package, and the at least one fill entry has a largest cross sectional area which is equal to or less than 25% of a largest cross sectional area of the compartment having the respective void space for which the fill entry forms the fluent entry. Each void space delimiting surface follows an outline of a separate 3D pill shape.

A package has a plurality of seamless compartments coupled together. A different one of the plurality compartments each includes a different respective one of a plurality of respective void spaces and a different respective one of a plurality of respective void space delimiting surfaces. A different one of a plurality of fill entries each forms a fluent entry into a different respective compartment's void space. At least one fill entry of said plurality is in an elastomeric portion of said package, and the at least one fill entry has a largest cross sectional area which is equal to or less than 25% of a largest cross sectional area of the compartment having the respective void space for which the fill entry forms the fluent entry. Each void space delimiting surface follows an outline of a separate 3D pill shape.

A method for operating a sealing station of a packaging machine, wherein the method may include one or more of the following steps: filling a packing volume of a package with a gas to create a desired atmosphere to a preset gassing target pressure for a finished package, wherein the packaging volume may be defined by a lower and an upper packaging material; discharging a partial amount of the gas introduced into the packaging volume from the packaging volume into a collection volume while retaining the packaging volume generated by the preceding filling, which reduces the pressure within the packaging volume; and reducing the packaging volume by moving the upper packaging material to an end position that corresponds to a desired appearance such that the pressure inside the package increases again to near the gassing target pressure. A sealing station that performs this method is also described.