A packaging assembly includes a case configured to at least partially contain injection devices for delivering a medicament; a light sensor configured to detect light incident on the packaging assembly; and a status indicator configured to generate an output which indicates a status of the packaging assembly conditional on an intensity of light detected by the light sensor exceeding a threshold light intensity.

When at least a part of a shaft portion of a plunger is stored in a proximal end side storage portion of a storage tray, the proximal end side storage portion supports a syringe body and the plunger in a state in which the syringe body and the plunger cannot approach each other since a first contact portion comes into contact with a proximal end surface of a body flange and a second contact portion comes into contact with a distal end surface of a pressing operation portion, and the part of the shaft portion of the plunger is prevented from separating since protruding pieces come into contact with the part of the shaft portion of the plunger.

This packaging device comprises a first stage (2a) of supporting units (20) configured to support a first plurality of medical containers (100a) in a first plane, a second stage (2b) of supporting units (20) configured to support a second plurality of medical containers (100b) in a second plane parallel to said first plane, the first plane and the second plane being spaced apart from each other so that the distal ends (106) of the first plurality of medical containers (100a) extend between medical containers of the second plurality of medical containers (100b), and the supporting units (20) of the first and second stages (2a, 2b) being configured so that the medical containers of the first and second pluralities of medical containers (100a, 100b) are oriented in a same direction. The first stage (2a) of supporting units (20) is formed by a first plate-shaped nest and the second stage (2b) of supporting units (20) is formed by a second plate-shaped nest.

A shielding member for use in sterilizing drug container assemblies includes a housing. The housing includes a first shielding portion and a second shielding portion. The first shielding portion includes a first and second surfaces and a plurality of first bore portions extending between. The second shielding portion having a first and second surfaces and a plurality of second bore portions corresponding to and aligned with the plurality of first bore portions. The first and second bore portions cooperate to form a plurality of receptacles including a plurality of openings in the first surface of the first shielding portion of the housing. The receptacles are sized and configured to receive drug container assemblies, each comprising a container with a container contact region and a seal member disposed adjacent the container contact region to seal the contents of the container at a sealing interface, such that each drug container assembly is exposed out of the housing through one of the openings.

To provide a medical device container, which enables transportation of a stored medical device in a fixed condition. A medical device container includes a container body having an opening portion at the upper portion; a holder, which is housed in the container body, for holding at least one medical device; and a gas non-permeable film sealing the opening portion of the medical device container; wherein the internal pressure of the medical device container is set to a value less than the atmospheric air pressure.

The present invention relates to a system for obtaining medicament related information of specific medicaments, the in system comprising a device (10, 50) for obtaining medicament related information, the device comprising a recording unit, said recording unit comprising a reader (20, 32; 86, 88, 92, 122), capable of reading information pertained to specific medicaments, said recording unit further comprising a memory module (22, 104) capable of storing information read by said reader (20, 32; 86, 88, 92, 122), wherein said reader (20, 32; 86, 88, 92, 122) is arranged with a three-dimensional contact interface (81) designed to interact with a corresponding contact surface (87) containing information related to specific medicaments.

An adapter assembly that includes a housing, a channel formed within the housing that is configured to receive a medical device, a first groove formed along an interior wall of the channel that is configured to at least partially receive a first retaining element, and a second groove formed along the interior wall of the channel that is configured to at least partially receive a second retaining element. The first retaining element is configured to extend outward from the first groove and the second retaining element is configured to extend outward from the second groove, such that the first and second retaining elements abut against the medical device received through the channel.

The present invention relates to a holding structure for simultaneously holding a plurality of containers for substances for pharmaceutical, medical or cosmetic applications or of devices having such containers, having a plurality of receptacles. The receptacles are arranged in a regular arrangement and are formed by in each case peripherally formed side walls. The receptacles have in each case one or two widened clearances having a dimension which is greater than the width of a gap between the containers received in the receptacles and side walls of the receptacles in the regions other than the widened clearances. The widened clearances additionally make available space for access to containers or devices which are received in the receptacles for handling thereof.

An on-body injector system includes a drug container assembly including a container, a seal member, and a sealing interface between the seal member and the container. The container includes an opening and the seal member at least partially covers the opening in the container. A fluid pathway assembly is coupled to the drug container assembly and includes a needle that is movable between a storage position, in which a point of the needle is spaced from the seal member, and a delivery position, in which the point of the needle is disposed at least partially through the seal member. A radiation generator is configured to emit rays of radiation to sterilize and/or disinfect the sealing interface. A barrier is disposed adjacent to the sealing interface and has an opening. At least a portion of the drug container assembly is positioned adjacent to the opening in the barrier.

A syringe cartridge including a reservoir part and an extension extending from the reservoir part. The extension defining a fluid path and including a molding and a first needle extending from the molding. The extension turning to a finite angle with respect to an axis of the reservoir part and at least part of the first needle is likewise at the finite angle. At least some of the part of the first needle at the finite angle being enclosed within the molding of the fluid path. A drug delivery device may be used with the cartridge and includes a skin-contacting surface. In use the longitudinal axis of the interior of the cartridge may be disposed substantially parallel to the skin-contacting surface.