Abstract: An apparatus includes a selectively actuated fluid system having a plurality of selected fluid reservoirs, for example replaceable cartridge-type fluid reservoirs. A first subset of the reservoirs can be selectively actuated to dispense an individual fluid from the selected reservoir. A second subset of the reservoirs can be simultaneously actuated to dispense two or more fluids in mixed form.

Abstract: A surgical retrieval apparatus includes a specimen retrieval bag including a rim movable from a collapsed configuration when positioned within a delivery tube to an automatically expanded configuration when advanced from the delivery tube. The rim is configured to receive a tissue specimen when the rim is in the expanded configuration. The retrieval bag defines a proximal portion with respect to the incision and a distal portion with respect to the incision. A specimen retrieval system further includes a delivery tube defining a longitudinal axis and includes the surgical retrieval apparatus contained therein that is configured to be inserted through a first opening in a patient's skin. The delivery tube defines an internal volume extending from a proximal end to a distal end of the delivery tube. The surgical retrieval apparatus is separable from the delivery tube.

Abstract: Drug delivery devices are described that include sensors and processing circuitry that can detect operating events, such as flow rates and drug delivery, in various types of inhalers, such as dry powder inhalers, metered dose inhalers, nasal inhalers and nebulisers. The information determined by the processing circuitry can be used to provide feedback to the user or can be stored or transmitted for subsequent analysis. This information can be used to improve clinical trials by providing information about the way in which the inhalers under test are being used.

Abstract: A method of retrieving a tissue specimen comprising inserting a surgical retrieval apparatus through an opening in a patient's skin, the surgical retrieval apparatus including a support member and a retrieval bag extending from the support member and having an opening to receive the tissue specimen. A net is introduced into the retrieval bag and placed over the tissue specimen. The net and retrieval bag are removed from the patient's body to remove the tissue specimen.

Abstract: An apparatus includes a selectively actuated fluid system having a plurality of selected fluid reservoirs, for example replaceable cartridge-type fluid reservoirs. A first subset of the reservoirs can be selectively actuated to dispense an individual fluid from the selected reservoir. A second subset of the reservoirs can be simultaneously actuated to dispense two or more fluids in mixed form.

Abstract: A method of retrieving a tissue specimen comprising inserting a surgical retrieval apparatus through an opening in a patient's skin, the surgical retrieval apparatus including a support member and a retrieval bag extending from the support member and having an opening to receive the tissue specimen. A net is introduced into the retrieval bag and placed over the tissue specimen. The net and retrieval bag are removed from the patient's body to remove the tissue specimen.

Abstract: A method of retrieving a tissue specimen comprising inserting a surgical retrieval apparatus through an opening in a patient's skin, the surgical retrieval apparatus including a support member and a retrieval bag extending from the support member and having an opening to receive the tissue specimen. A net is introduced into the retrieval bag and placed over the tissue specimen. The net and retrieval bag are removed from the patient's body to remove the tissue specimen.

Abstract: Drug delivery devices are described that include sensors and processing circuitry that can detect operating events, such as flow rates and drug delivery, in various types of inhalers, such as dry powder inhalers, metered dose inhalers, nasal inhalers and nebulisers. The information determined by the processing circuitry can be used to provide feedback to the user or can be stored or transmitted for subsequent analysis. This information can be used to improve clinical trials by providing information about the way in which the inhalers under test are being used.

Abstract: A surgical access assembly for positioning within an opening in a tissue to provide access to a patient's body for insertion of surgical instrumentation therethrough. The surgical access assembly includes a body portion defining a longitudinal axis and a passageway and having a proximal portion and a distal portion. At least a portion of the distal portion is configured to transition from a more flexible, first configuration for passage into a patient's body and a more rigid, second configuration to securely maintain the distal portion within the patient's body.

Abstract: A surgical access assembly having a body including a leading end, a trailing end, and first and second body members extending between the leading and trailing ends. The leading end, trailing end and first and second body members define a passageway therethrough for receipt of surgical instrumentation. First and second flexible wing members extend proximally from the body. A flexible member is attached to the body and extends proximally therefrom.

Abstract: A method of retrieving a tissue specimen comprising inserting a surgical retrieval apparatus through an opening in a patient's skin, the surgical retrieval apparatus including a support member and a retrieval bag extending from the support member and having an opening to receive the tissue specimen. A net is introduced into the retrieval bag and placed over the tissue specimen. The net and retrieval bag are removed from the patient's body to remove the tissue specimen.

Abstract: An ostomy appliance is described in the form of a controlled discharge device for controlling discharge from the stoma and/or an ostomy pouch for collecting discharged waste. The appliance may include one or more of: an elastomeric stoma seal for providing a seal around or directly against the stoma; a stoma occluder for occluding the stoma without passing internally into the stoma; a peristomal foam wall; a confinement seal for confining at least solid excreta to a confinement region adjacent to the stoma; a stowable collector bag; and interchangeable controlled discharge devices and ostomy pouches. The foam wall may provide a barrier to stool, but allow escape of flatus. The foam wall and/or the stoma occluder and/or the confinement seal may apply a force in a direction to increase the sealing force on the stoma seal.

Abstract: An ostomy appliance is described in the form of a controlled discharge device for controlling discharge from the stoma and/or an ostomy pouch for collecting discharged waste. The appliance may include one or more of: an elastomeric stoma seal for providing a seal around or directly against the stoma; a stoma occluder for occluding the stoma without passing internally into the stoma; a peristomal foam wall; a confinement seal for confining at least solid excreta to a confinement region adjacent to the stoma; a stowable collector bag; and interchangeable controlled discharge devices and ostomy pouches. The foam wall may provide a barrier to stool, but allow escape of flatus. The foam wall and/or the stoma occluder and/or the confinement seal may apply a force in a direction to increase the sealing force on the stoma seal.

Abstract: An ostomy appliance is described in the form of a controlled discharge device for controlling discharge from the stoma and/or an ostomy pouch for collecting discharged waste. The appliance may include one or more of: an elastomeric stoma seal for providing a seal around or directly against the stoma; a stoma occluder for occluding the stoma without passing internally into the stoma; a peristomal foam wall; a confinement seal for confining at least solid excreta to a confinement region adjacent to the stoma; a stowable collector bag; and interchangeable controlled discharge devices and ostomy pouches. The foam wall may provide a barrier to stool, but allow escape of flatus. The foam wall and/or the stoma occluder and/or the confinement seal may apply a force in a direction to increase the sealing force on the stoma seal.

Abstract: A secure housing for an electronic unit, in particular a franking machine has a first housing part and a second housing part releasably connected to the first housing part via at least one connecting device. In order to prevent the housing from being opened without leaving trace of the opening, there is provided at least one covering device on and/or in the first or second housing part. The covering device blocks the access to the connecting device and can only be removed from the first or second housing part with noticeable damage being caused.

Abstract: A secure housing for an electronic unit, in particular a franking machine has a first housing part and a second housing part releasably connected to the first housing part via at least one connecting device. In order to prevent the housing from being opened without leaving trace of the opening, there is provided at least one covering device on and/or in the first or second housing part. The covering device blocks the access to the connecting device and can only be removed from the first or second housing part with noticeable damage being caused.

Abstract: A secure housing for an electronic unit, in particular a franking machine, has a first housing part and a second housing part releasably connected to the first housing part via at least one connecting device. In order to prevent the housing from being opened without leaving trace of the opening, there is provided at least one covering device on and/or in the first or second housing part. The covering device blocks the access to the connecting device and can only be removed from the first or second housing part with noticeable damage being caused.

Abstract: An ostomy appliance is described in the form of a controlled discharge device for controlling discharge from the stoma and/or an ostomy pouch for collecting discharged waste. The appliance may include one or more of: an elastomeric stoma seal for providing a seal around or directly against the stoma; a stoma occluder for occluding the stoma without passing internally into the stoma; a peristomal foam wall; a confinement seal for confining at least solid excreta to a confinement region adjacent to the stoma; a stowable collector bag; and interchangeable controlled discharge devices and ostomy pouches. The foam wall may provide a barrier to stool, but allow escape of flatus. The foam wall and/or the stoma occluder and/or the confinement seal may apply a force in a direction to increase the sealing force on the stoma seal.

Abstract: A printing device, in particular a franking machine, has a print head that can be moved along a first direction into a first longitudinal position, and a station that cooperates with the print head in the first longitudinal position. The print head is cleaned and/or maintained and/or retained and preserved at the station. The print head is designed and/or arranged to move toward the station in a second direction that extends transversely with respect to the first direction in order to cooperate with the station.

Abstract: The franking machine has a clamping device which can be driven via a drive device and which securely clamps an item of mail to be franked against a stop element. The clamping device has a clamping unit, which is provided for interacting with the item of mail, and a gearing device which is connected to the clamping unit and the drive device. The gearing device displaces the clamping unit in the direction of the stop element. The clamping unit and/or the gearing device have at least one compensation section which is configured elastically such that, in the case of a predetermined drive displacement of the drive device, compensation for different thicknesses of the item of mail is provided by elastic deformation of the compensation section.