A non-destructive measurement unit of gas concentration in sealed containers and an automatic filling and/or packaging line using such a unit are provided. The flexible containers are at least partially optically transparent, and the measurement unit comprises a light source for emitting a light beam at a wavelength tunable with an absorption wavelength of a gas contained in the sealed flexible container. The light source directs the light beam toward at least one inspection area, and a detector detects at least a portion of the beam after the beam passes through the inspection area and outputs data representative of an absorption spectrum of the gas. Means for generating a head space of predefined width into the sealed flexible container is adapted to advance the sealed flexible container by an advancement path which crosses the inspection zone and to maintain the predefined width of the head space during the advancement.

Example aspects of a bicycle packaging and a method for assembling a bicycle packaging are disclosed. The bicycle packaging can comprise a first packaging body comprising a primary fastener and a secondary mating fastener; and a second packaging body comprising a secondary fastener and a primary mating fastener, the first packaging body and second packaging body defining a void, the primary fastener engaging the primary mating fastener, and the secondary fastener engaging the secondary mating fastener.

An apparatus for closing a flap on an open end of a box may include a device having a slot and a mechanism operable to provide a relative motion between the slot and the flap. The relative motion may cause the flap to be received into the slot and the flap to be reoriented to a closed position. A method of closing an open end of a box being conveyed downstream, with the open end facing transversely, may include two operations. With a trailing minor flap on the open end being held in a substantially upstream-pointing open position, the opposing leading minor flap on the open end may be closed from a substantially downstream-pointing open position to a substantially upstream-pointing closed position. With the leading minor flap being held in the closed position, the trailing minor flap may be closed from the open position to a substantially downstream-pointing closed position.

A container (100) includes a first side (101) defining an aperture (107), a second side (102), and a plurality of other sides (103,104,105). The first side, the second side, the plurality of other sides defining an interior volume (106) of the container. A plurality of gloves (1001) is disposed within the interior volume such that one or more gloves may be drawn from the container through the aperture. An antimicrobial coating (302) disposed upon one or more of the first side, the second side, and the plurality of sides.

A container (100) includes a first side (101) defining an aperture (107), a second side (102), and a plurality of other sides (103,104,105). The first side, the second side, the plurality of other sides defining an interior volume (106) of the container. A plurality of gloves (1001) is disposed within the interior volume such that one or more gloves may be drawn from the container through the aperture. An antimicrobial coating (302) disposed upon one or more of the first side, the second side, and the plurality of sides.

A medicine packaging apparatus 10 has a packaging paper supplying part 42; a sealing device 50 for forming a packaging bag; a medicine introducing part 80 for introducing the medicines M from an opening portion of the packaging bag P in an unsealed-state; a detecting part 90 for detecting presence of the medicines M in an introducing path for the medicines M by the medicine introducing part 80 and a determining part which can determine that a packaging failure occurs under a condition that the presence of the medicines M is detected by the detecting part 90 within a time period after a timing of starting to seal the packaging bag P in which the medicines M have been introduced and before a timing of introducing the medicines M to be packaged in a subsequent packaging bag P through the medicine introducing part 80.

A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. Printed instructions (1001) can be included with the tray (100). One or more layers of wrap material (2200) can be folded about the tray (100) to enclose the tray (100) and other items, such as an additional layer of wrap material (2701), packaged liquid hand sanitizer (2401), and packaged gloves (2402). When a health care services provider (3101) unfolds the wrap material, the same can be used to create a sterile field beneath a patient (3201).

This disclosure describes example adhesive medical patches that may be used in combination with one or more antimicrobial agents to create and/or maintain an area of human skin that is free from contaminants. According to some embodiments, the disclosure describes that the adhesive patches may contain an adhesive material affixed to the perimeter of an impermeable backing According to some embodiments, the adhesive patch may also have a permeable layer containing an antimicrobial agent located interior to the adhesive material on the impermeable backing.

This disclosure describes example adhesive medical patches that may be used in combination with one or more antimicrobial agents to create and/or maintain an area of human skin that is free from contaminants. According to some embodiments, the disclosure describes that the adhesive patches may contain an adhesive material affixed to the perimeter of an impermeable backing According to some embodiments, the adhesive patch may also have a permeable layer containing an antimicrobial agent located interior to the adhesive material on the impermeable backing.

A system for packaging dosed quantities of solid drug portions comprises a plurality of dosing stations (2) for dispensing a dosed quantity of solid drug portions, a plurality of guiding ducts (7), a plurality of collecting containers (17) for receiving drug portions guided through the guiding ducts (7), and at least one discharge and packaging station (3) for transferring drug portions collected by each collecting container (17) to a packaging and for closing the packaging. The guiding ducts (7) are coupled to a transport means (6a, 6b, 8, 10, 11, 12, 15, 16) for moving the guiding ducts (7) along the dosing stations (2), wherein each guiding duct (7) is adapted to receive drug portions dispensed from at least one of the dosing stations (2) when the guiding duct (7) is positioned at the at least one dosing station (2), and to guide the received drug portions to an passage opening of the guiding duct (7). The collecting containers (17) are also coupled to the transport means (6a, 6b, 8, 10, 11, 12, 15, 16) so that each collecting container (17) can be positioned at the passage opening of one of the guiding ducts (7) to receive drug portions guided through the guiding duct (7).