Abstract: A method for fabricating an article of headwear for a subject is provided. The method comprises: generating a three-dimensional digital data file for the subject at a clinic by capturing a three-dimensional data file representative of the head by utilizing apparatus located at the clinic operating to capture three-dimensional data representative of the head; utilizing a processor to process the three-dimensional digital data file to produce a device file comprising the shape for the article of headwear; and manufacturing the article of headwear at the clinic by utilizing an additive manufacture device located at the clinic to operate with the three-dimensional digital data file.

Abstract: A custom cranial remodeling device to correct a deformed head of a subject comprises an inner layer shaped to contact the head of the subject at predetermined areas, the inner layer is deposited by an additive manufacturing device and an outer layer deposited by the additive manufacturing device. The inner layer and the outer layer are each formed by the additive manufacture device utilizing a device data file derived from a subject data file, the subject data file representative of the shape of the deformed head, the device data file determining the shape of the cranial remodeling device to correct the shape of the deformed head.

Abstract: Custom manufactured headwear for a subject's head is provided. The headwear comprises an inner layer shaped to contact the head of the subject at predetermined areas. The inner layer is deposited by an additive manufacturing device. The headwear further comprises an outer layer deposited by the additive manufacturing device. The inner layer and the outer layer are each formed by the additive manufacture device utilizing a device data file derived from a subject data file. The subject data file is representative of the shape of the head and the device data file determining the shape of the headwear.

Abstract: A garment for long duration waste removal includes, among other things, a containment layer, a containment interface defining a passage, a storage container extending from the containment interface, and a cleansing member routed through the passage, and into the storage container. The cleansing member is moveable relative to the containment layer to remove solid waste. A waste management system for long duration vehicle operations is also disclosed.

Abstract: A garment that heats a portion of a human body during warm-up prior to athletic endeavor having a heater pad member with a size between the size of a common index card and an ordinary sheet of paper for localized penetrating heating of tissue and muscles. Heating is achieved by electrical heating of a heater pad member having a reflective metal foil on one side of the heater pad and thermally conductive PVF sheets on the opposite side. On the one hand, the metal foil reflects optical radiation toward a human body, while on the other hand, the PVF sheets direct infrared radiation into the human body. Control electronics, a battery and the heater pad are contained in separate pockets of the garment that are electrically connected together.

Abstract: A thermal control unit for controlling a patient's temperature includes a fluid outlet for delivering temperature-controlled fluid to a patient, a pump, first and second cooling units, and a controller that selectively enables and disables at least one of the cooling units based on one more factors, such as the temperature of the fluid. Alternatively or additionally, a variable speed fan is included in one or both of the cooling units that blows air over the condenser and the controller selectively controls the fan speed based on factors such as the temperature of the circulating fluid. The thermal control unit may be modified to accept a cartridge having its own cooling unit. When so modified, the controller communicates with a controller inside of the cartridge and coordinates control of the cartridge cooling unit and the cooling unit inside the thermal control unit that is external to the cartridge.

Abstract: Apparatus to treat an eye comprises an annular retention structure to couple to an anterior surface of the eye. The retention structure is coupled to a suction line to couple the retention structure to the eye with suction. A coupling sensor is coupled to the retention structure or the suction line to determine coupling of the retention structure to the eye. A fluid collecting container can be coupled to the retention structure to receive and collect liquid or viscous material from the retention structure. A fluid stop comprising a porous structure can be coupled to an outlet of the fluid collecting container to inhibit passage of the liquid or viscous material when the container has received an amount of the liquid or viscous material. The coupling sensor can be coupled upstream of the porous structure to provide a rapid measurement of the coupling of the retention structure to the eye.

Abstract: Apparatus to treat an eye comprises an annular retention structure to couple to an anterior surface of the eye. The retention structure is coupled to a suction line to couple the retention structure to the eye with suction. A coupling sensor is coupled to the retention structure or the suction line to determine coupling of the retention structure to the eye. A fluid collecting container can be coupled to the retention structure to receive and collect liquid or viscous material from the retention structure. A fluid stop comprising a porous structure can be coupled to an outlet of the fluid collecting container to inhibit passage of the liquid or viscous material when the container has received an amount of the liquid or viscous material. The coupling sensor can be coupled upstream of the porous structure to provide a rapid measurement of the coupling of the retention structure to the eye.

Abstract: Disclosed herein are drug delivery devices and methods for the treatment of ocular disorders requiring targeted and controlled administration of a drug to an interior portion of the eye for reduction or prevention of symptoms of the disorder. In several embodiments, the devices are configured to release a pro-drug form of a drug into a target tissue site, wherein the pro-drug is converted to an active drug that yields a therapeutic effect. The use of the device and pro-drug form advantageously, in several embodiments, provide a stable drug composition that can yield a therapeutic effect over an extended time period.

Abstract: Devices can be implanted in an eye to treat a dry eye condition. The devices include a body defining a lumen and having first and second ends and external and lumenal surfaces. The body has a length sufficient to provide fluid communication between the anterior chamber and tear film of the eye through the lumen when the device is implanted in the sclera. In some embodiments, the device is filterless. In some embodiments, a filter is included. The dry eye treatment devices provided herein prevent bacterial ingress, provide outflow resistance to retain a normal intraocular pressure, and provide moisture (e.g., aqueous humor) to an otherwise dry eye. Methods of treating a dry eye condition wherein the device is implanted in the sclera of an afflicted eye are also described.

Abstract: Providing neuroprotective therapy for glaucoma includes generating a micropulsed laser light beam having parameters and characteristics, including pulse length, power, and duty cycle, selected to create a therapeutic effect with no visible laser lesions or tissue damage to the retina. The laser light beam is applied to retinal and/or foveal tissue of an eye having glaucoma or a risk of glaucoma to create a therapeutic effect to the retinal and/or foveal tissue exposed to the laser light beam without destroying or permanently damaging the retinal and/or foveal tissue and improve function or condition of an optic nerve and/or retinal ganglion cells of the eye.

Abstract: Head worn devices having a variable shade component and a fixed shade component, and methods of operation, are disclosed. An example head worn device includes an auto-darkening lens configured to adjust a shade value within a first shade value range, a second lens having a fixed shade value greater than 0, the auto-darkening lens and the second lens overlapping in a field of view of the head worn device to result in a net shade value range in the field of view that is greater than the first shade value range, and a clear lens on an exterior of the auto-darkening lens and the second lens.

Abstract: [Problem] The present invention provides a preparation jig for a tympanic membrane regenerating agent and a preparation vessel for a tympanic membrane regenerating agent enabling simple preparation of a tympanic membrane regenerating agent. [Solution] A preparation jig for a tympanic membrane regenerating agent (1a) and a preparation vessel for a tympanic membrane regenerating agent (1A) each include: a vessel (3A) including housing walls (6, 7) forming an interior space (S1) housing a medicinal solution support (2), and including an opening (6h) opening in one direction and formed in the housing walls (6, 7); and a holding portion (4A) disposed in the interior space (S1). The deep side of the interior space (S1) is a housing portion (S3) housing the medicinal solution support (2) holding a medicinal solution. The opening (6h) side of the interior space (S1) is an installation space (S2) in which the holding portion (4A) is disposed.

Abstract: A noise reductions device is provided the device includes an outer member having an inlet opening and an outlet opening; a hollow spherical member mounted in the opening and configured for mixing sound waves; a cannula having an inlet tip in communication with the hollow spherical member, and an outlet tip configured for transmitting sound waves therethrough; wherein the cannula includes at least one winding between the inlet tip and the outlet tip.

Abstract: Systems, methods, and apparatuses for generating and releasing iodine are described. Some embodiments may include a dressing member including a plurality of iodine-forming reagents and a water-swellable material. In some embodiments, the dressing member may include water-swellable fibers. The water-swellable fibers may each include a water-swellable material in which iodine-forming reagents are dispersed. As liquid comes into contact with and is absorbed by the water-swellable material, the iodine-forming reagents may come into contact with each other, causing an iodine-forming reaction to occur, producing iodine.

Abstract: Antimicrobial coating compositions are used to form dried residual antimicrobial coatings on medical dressings including gauze, bandages, gowns and dry wipers. Antimicrobial coating compositions comprise at least one of an organosilane (R1O)3Si—R2—Z, an organic amine R9R10R11N a titanium (IV) species, a 1,2-diol, an ?-hydroxy acid, a ?-hydroxy acid, and an organosilane grafted parylene polymer, wherein R1 is H, alkyl, substituted alkyl, aryl or substituted aryl, R2 is a bivalent linker, Z is a nucleophile, leaving group, or quaternary nitrogen substituent and R9, R10, and R11 are independently H, alkyl, substituted alkyl, aryl, substituted aryl or cyclic.

Abstract: A pressure switch for controlling application of negative pressure to dressing disposed adjacent a tissue site is disclosed. The pressure switch comprises a body having a base, sidewalls extending from the base to an open end, and an inlet coupled to the dressing and forming a passage through the body. The pressure switch further comprises a diaphragm closing the open end of the sidewalls and forming a vacuum chamber with the body, wherein the inlet fluidly couples the vacuum chamber and the dressing. The pressure switch further comprises a valve disposed in the passage and configured to restrict the flow of gas through the passage so that a switch pressure developed in the vacuum chamber as a result of the application of negative pressure to the dressing lags a wound pressure at the tissue site to delay, wherein the diaphragm is adapted to be operatively responsive to the switch pressure to move between a relaxed position and a compressed position as the negative pressure increases and decreases.

Abstract: Systems, methods, and devices are presented for treating a tissue site and managing hair proximate the tissue site. A composition is provided for inhibiting, removing, or weakening hair proximate the tissue site and for providing an improved fluid seal by a flexible film drape over the tissue site. In some example embodiments, a hair-modification agent is disposed at least proximate a peripheral edge of a treatment manifold between a drape and epidermis proximate a tissue site. The hair-modification agent can be configured to flow over imperfections on the epidermis and to form a fluid seal against the epidermis, and can further be configured to at least substantially weaken hair on the epidermis as the hair encounters the hair-modification agent.

Abstract: An external fixation device for body includes a front part and a back part and can be shaped according to the shape of human body. The front part includes a cavity, two layers of knitting cloth, and elastic belts. The back part includes a cavity, two layers of knitting cloth, and plackets. The lower end edge of the front part and the lower end edge of the back part are respectively provided with a filling port and the filling ports are both sewed with a hook and loop. An outer side of one of the elastic belts of the front part and an inner side of one of the plackets of the back part are respectively provided with a piece of a first fastener. An armhole width part of the front part and an armhole width part of the back part are respectively provided with a piece of a second fastener.

Abstract: Elastic band products of high durability and quality are disclosed. Also disclosed are methods of producing durable, high quality elastic band products using modified anvil blocks, including shaped anvil blocks, anvil blocks with lateral protuberances and/or anvil blocks with teeth. The disclosed methods result in reduced elastic yarn thread slippage both during production and in the finished elastic band product.

Abstract: An x-ray detectable fabric comprising: a first set of fibers having a rayon composition; a second set of fibers having a polymeric composition with an x-ray detectable material impregnated therein; wherein the first and second sets of fibers are in an entangled state as a cohesive porous fabric, and wherein fibers in the second set of fibers are distributed throughout the fabric. In particular embodiments, the first and second sets of fibers are in a non-woven state, with a bonding agent maintaining adhesion between the fibers. The polymeric composition in the second set of fibers may be selected from, for example, vinyl addition polymers, polyesters, rayon, nylon, and cellulosic compositions. The first set of fibers may or may not also include an x-ray detectable material.

Abstract: The invention features a disposable absorbent article including a thermoplastic composition applied in a full coat layer (i.e. a layer with 100% coverage) as a discrete shape to either the top sheet or to a component of the absorbent core (i.e. core or core wrap). The discrete shape is strategically located to decrease the likelihood of leaks in the desired location. The thermoplastic composition serves as a leak barrier to prevent bodily fluids and solids (i.e. urine, stool, menstrual flow, wound seepage) from leaking from the absorbent core.

Abstract: To provide a user-friendly disposable article including a disposable base fabric provided with at least one of a permeable sheet and a fiber sheet, and multiple elastic members that are joined to at least one of the permeable sheet and the fiber sheet so as to have a joined part and a non-joined part; and a joining part for joining the disposable base fabric and an article to be attached so that the multiple elastic members give an elastic force to a surface to be applied to the skin, arranging the disposable base fabric on the surface side for applying to the skin.

Abstract: An underpants-type disposable diaper includes outer members 12F and 12B having stretchable regions A2 and A3 disposed adjacent to the inner edges of the side seal portions 12A in the width direction. The stretchable regions A2 and A3 include multiple elongated elastically stretchable members 19 disposed between two sheet layers 12S and 12H at predetermined intervals in the front-back direction and extending in the width direction. The elastically stretchable members 19 each include two fixed ends 19f fixed to the two sheet layers 12S and 12H, and the section between the fixed ends 19f is unfixed to the two sheet layers 12S and 12H. The two sheet layers 12S and 12H are welded into sheet bonding sections 20, at positions between the elastically stretchable members 19 in the stretchable regions A2 and A3 adjacent is the front-back direction. No sheet bonding section protrudes from the side seal portion in the stretchable regions A2 and A3.

Abstract: An absorbent article. The absorbent article includes a topsheet having a body contacting surface, a backsheet joined to said topsheet, and an absorbent core disposed between the topsheet and the backsheet, wherein the absorbent core has an upper layer and a lower layer. The lower layer has two density zones.

Abstract: The present invention provides a wrapping device for wrapping body parts. Said wrapping device comprises a rotation module having a first roller ring, a second roller ring, and a plurality of connecting parts; a driving module driving at least one of the first roller ring and the second roller ring to revolve; and at least a pressing device disposed on the second roller ring. In said wrapping device, the first roller ring and the second roller ring are separately and coaxially disposed, while the opposite ends of each of the plurality of connecting parts are separately connected to the first roller ring and the second roller ring. In addition, the first roller ring includes a first ring hole surrounded and formed by a first inner ring wall, and the second roller ring includes a second ring hole surrounded and formed by a second inner ring wall. Said at least a pressing device protrudes toward an inner space of the second ring hole.

Abstract: A patient transport apparatus comprises a support structure. The support structure comprises a base, a frame, and a patient support surface to support a patient. One or more handle assemblies are coupled to the frame to maneuver the patient transport apparatus. The handle assemblies comprise one or more handles to be manipulated by a user. The handles are capable of being adjusted to facilitate maneuvering of the patient transport apparatus, such as pushing/pulling the patient transport apparatus along a floor surface, lifting the patient transport apparatus over obstacles, loading the patient transport apparatus into an emergency vehicle, and/or unloading the patient transport apparatus from the emergency vehicle.

Abstract: The present disclosure describes devices and systems that can be integrated with a foldable, manual wheelchair to convert the wheelchair into a hybrid chair capable of both manual operation and motor-powered operation. A wheelchair powering device includes a motor that is operatively coupled to a roller member so that rotation of the motor shaft causes rotation of the roller member. The roller member may be engaged against a tire of the wheelchair so that rotation of the roller member causes rotation of the tire via friction between the roller member and tire.

Abstract: A system for monitoring activity level of a wheeled vehicle while being manually propelled by a user includes a sensor, a wireless transmitter, and a base supporting the sensor and the transmitter. The base is mountable to a wheel of the wheeled vehicle. The wireless transmitter wirelessly transmits a plurality of data corresponding to sensor information received from the sensor regarding motion of the wheel over time. A remote computing device receives the data and dynamically determines a wheel-motion value according to the data. When the wheel-motion value is within a predetermined percentage of a predetermined maximum motion value, the remote computing device issues an alert to the user. If the wheel-motion value corresponds to motion of the wheel at a current time, the alert may be issued substantially in real time to alert the user that they may be over-exerting themselves.

Abstract: The present disclosure relates to a tilt assembly (i) for a powered wheelchair (15), comprising: an elongated base member (3) provided with an axial channel, a lifting member (5) configured to be received by the base member (3) and to move rectilinearly in the channel, between a retracted position and an extended position relative to the base member (3), a tilt frame (7) pivotally connected to the lifting member (5), the tilt frame (7) being configured for mounting a seat assembly (21) thereto, and an arm (9) pivotally connected to the base member (5) and to the tilt frame (7), wherein the tilt frame (7) is configured to obtain a perpendicular orientation relative to a central axis (ii) of the lifting member (5) when the lifting member (5) is in the retracted position and to be inclined relative to the central axis (ii) when the lifting member (5) is in the extended position, to thereby provide a tilt functionality.

Abstract: The invention provides a contouring system configured to be modified to provide a support surface, such as a backrest, seat base, or mattress, having contours to suit the needs of its user.

Abstract: A wheelchair assembly that enables an occupant to rotate their self from the seating position to the prone or kneeling prone position so that the occupant may use their arms to better reach and grasp without the aid of another person.

Abstract: A bed includes a frame installed horizontally with respect to a floor, a plate installed over the frame and having an end portion that is inclined upward with respect to the frame, an arm that supports the plate over the lower side of the plate, and a sensor attached to the arm.

Abstract: An apparatus for rotating a bed-ridden person in order to prevent pressure sores, or bed sores, comprising an first set of bladders and a second set of bladders, and at least one fluid pump, which may be an air pump, in fluid communication with the bladders through a system of fluid valves. Inflating first set of bladders will cause a patient to be rotated onto their right side; likewise, inflating the second set of bladders will cause a patient to be rotated onto their left side. A patient may therefore be rotated from left side to right side in order to prevent pressure, or bed, sores from occurring. The invention may be programmed to rotate persons automatically on any predetermined timing, and in any sequence, desired, or by manual command. The invention also comprises a pump and valve assembly for low pressure applications.

Abstract: A mobility aid assembly for lifting and lowering a user; the assembly including an articulated lifting arm releasably mounted to a base structure; a first portion of the lifting arm operable between a lowered position and a raised position by a linear actuator; a first end of the linear actuator pivotally connected to the first portion of the lifting arm and, wherein a second end of the linear actuator is releasably mounted so as to avoid injury to the user if the linear actuator moves the first portion of the lifting arm to an excessively lowered position in which the first portion of the lifting impinges on the user.

Abstract: A patient lift system helps to lift and mobilize a disabled person in a home or in an institution with minimal effort from a caregiver. The patient lift system includes a lift, a carry bar and a hand control. The lift, the carry bar and the hand control have shapes and features that may be seen to facilitate quick and easy cleaning. Notably, gaps have been minimized for infection control purposes. Typically, a patient lift system includes an integral trolley for connecting the patient lift system to a track. For the patient lift system described herein, the trolley and lift system are separate pieces that are easily and quickly either attached or detached.

Abstract: An orthopedic post pad comprising: an inner cushion layer, the inner cushion layer having a lune shape with a first peak, and a second peak; a post hole located in the inner cushion layer on a side opposite the two peaks; an outer cushion layer enveloping the inner lateral surface and concave surface of the inner cushion, the outer cushion layer and inner cushion layer together generally forming a right cylindrical shape.

Abstract: A robotized bed according to one or more embodiments may include a table for placing a patient, and a robotic arm supporting and moving the table, wherein the robotic arm includes a base, a plurality of joints and a plurality of actuators each of which drives each of the joints, wherein the robotic arm moves the table between an MRI scanning position for imaging a patient by an MRI apparatus or an MRI scanning preparation position which is different from the MRI scanning position, and a treatment position for a doctor to treat a patient, wherein the treatment position is a position located away from the MRI apparatus by a predetermined distance or more.

Abstract: Some embodiments described herein relate to a surgical table, specifically a base of a surgical table. The surgical table can be adapted to include and/or be coupled to a surgical robot. The base of the surgical table can form an enclosure including a cover and a bottom. Electronic components (e.g., power electronics associated with the surgical robot) can be disposed within the enclosure. In some embodiments described herein, the cover of the base of the surgical table can be constructed of aluminum or similar material having a thermal conductivity of at least 200 W/m K. In some embodiments described herein, a side wall of the base of the surgical table can be constructed of aluminum or similar material having a thermal conductivity of at least 200 W/m K. Other embodiments described herein describe various other solutions for thermal management of electronic components.

Abstract: The present disclosure generally relates to intelligent garments that provide thermal regulation in a variety of environments. The garments may include different layers such as a hydrophobic layer in direct contact with a wearer's skin surface and saturated with an aqueous mixture, a spacer layer, a reflective layer, and an outer hydrophobic layer. The layers of the garment may work together to reduce the metabolic expenditure of the wearer in extreme environmental conditions or during demanding physical activity. A variety of sensors may be displaced throughout the garments so as to enable the collection of data associated with wearers as well as environmental conditions. Wearers may control the thermal balance and other properties of the garments as desired.

Abstract: A collapsible upright wheeled walker with adjustable armrests that support sufficient user upper-body weight to facilitate a natural upright gait and provide unassisted mobility for a wide range of mobility-impaired individuals. The apparatus may be easily and quickly folded (and unfolded) and may include bilateral stabilizing wheel suspensions to facilitate navigation over uneven terrain. The apparatus includes a frame-stiffening folder assembly and may also include mechanical brakes, an adjustable upper armrest assembly with removable padded forearm supports and two pairs of handles, at least one of which is disposed sufficiently forward to place the user within the polygonal footprint defined by the front and rear wheels to provide support without leaning, stooping, or risking falls.

Abstract: Transducers for applying stimulation to a patient include a Peltier device (8), a pneumatically inflatable Finger bladder (4) and an LRA or ERM (6), and are connected to a controller. In a passive mode stimulation can be provided in the absence of feedback from the patient. In an active mode, the addition of movement detection enables additional visual images to encourage a response from a patient, increasing the range or rehabilitation provided to the patient.

Abstract: A portable massage table and recovery device may feature a support table and independent massage head mounted within a slot in said support table. Both massage head and support table are supported upon the ground and the support table is capable of independent rolling motion in-line with the massage head. The massage head may be compressible with varying levels of resistance and may feature an articulable massage structure. Side rolling wheels may be used to maintain the in-line relationship of the massage head and support table.

Abstract: A self-operated, or therapist assisted, apparatus particularly adapted for massaging a user's body parts affected by repetitive strain injuries such as tendinitis and carpal tunnel syndrome, comprises two clamping arms joined at a base end and provided with an opening at the other end. Flexible massaging members are mounted on opposite medial sections of the arms. A body part may be placed between the two arms of the device to be acted upon by the massaging members, whereby the body part is adjustably clamped between the pair of massaging members and massaged by translating and rotating movements of the body part along an axis perpendicular to the mounting axes of the massaging members. Alternatively, one of the arms of the apparatus may be separated from the apparatus and used independently to massage body parts that otherwise would not fit between the arms of the apparatus.

Abstract: A sexual stimulation device includes a main body having a generally blunt first end, a top surface, a bottom surface, and a dildo that extends outward from the bottom surface of the main body. The dildo including a curved shaft that forms an obtuse angle. A flap is positioned along the bottom surface adjacent to the second dildo. One or more removable and reconfigurable handles are secured to the blunt first end of the main body.

Abstract: An invasive shock wave applicator for applying shock waves sideways includes a bar-shaped invasive member and a disk. The invasive member defines a lateral side, has a first end with a recess extending inward from the lateral side, and is provided with a shock wave transmission member detachably sealing the opening of the recess. The disk is embedded in the invasive member; divides the recess into first and second receiving rooms, which are adjacent to and away from the shock wave transmission member respectively; and is provided with a vibration plate adjacent to the first receiving room and facing the shock wave transmission member. The first receiving room is filled with a shock wave transmission medium. Shock waves propagate toward the lateral side of the invasive member to facilitate the performance of an invasive shock wave treatment in a human cavity of the human body.

Abstract: An automatic pipe clean system for massage bath equipment includes a bathtub, a water-filling pipe, a water-draining pipe, a suction pipe, a pump pipe, a pump connected between the suction pipe and the pump pipe, an automatic water-filling pipe, a water-filling valve and a controller. The controller is configured to: in a cleaning stage: turn on the pump to allow the water to pass and clean the suction pipe and the pump pipe; and in a drying stage: turn on the pump to allow the water to drain out from the suction pipe and the pump pipe; and turn off the pump.

Abstract: A vaporizing and vapor heating assembly includes at least one vaporizing element fluidically coupled to at least one reservoir and configured to discharge vapor and a heater assembly operably coupled to the at least one vaporizing element. The heater assembly including at least one heating element configured to heat the discharged vapor.

Abstract: The present invention relates to a fluid dispensing container in the field of enteral nutritional feeding, and in. particular to a dispenser for dispensing of a supplemental enteral fluid to a subject. Particularly, the invention provides a small-volume dispenser p refilled with an enteral fluid, which can be coupled with a feeding or medical tube port. Preferably, the enteral fluid is a composition of omega-3 fatty acids. The invention further provides a method for administering an enteral fluid to a subject using such dispenser. Yet further, the invention provides a method for supplementing an enteral nutritional product with an enteral fluid using such dispenser.

Abstract: The present disclosure provides a port. In an embodiment, a port is provided and includes (i) an optional top portion, (ii) a base, and a channel extending through the optional top portion and the base for passage of a flowable material, and (iii) a septum extending across the channel. The septum comprises an ethylene/?-olefin multi-block copolymer.