Abstract: An isolation container includes an isolation space for receiving an object and maintains the isolation space substantially isolated while providing for continuous access to, and maneuverability within, the isolation space through one or more access ports. An air management system re-circulates air through the isolation space to create a negative or positive pressure within the space, and is operable to filter, and optionally adjust the temperature and humidity of, the re-circulating air. In an embodiment of the isolation container configured for transporting a patient in the isolation space, a communications system is also coupled to the isolation space to provide for audio, video or other data communications between the patient and a communications device external to the isolation container.

Abstract: There are occasions when a medical facility has the need to image subject that have been contaminated with a hazardous or communicable chemical or biological agent. Occurrences of such conditions are often too remote to justify having diagnostic scanners dedicated to such imaging. A contaminated or “hot” chamber (20) interfaces with one or more uncontaminated imaging suites or “cold” chambers (22). The hot chamber (20) includes barrier walls (16) with selectively deployable containment tubes (14) that when deployed, are sealed with the barrier wall (16) and extend from the barrier wall into the gantry of the cold chamber scanners. The tubes (14) extend the hot chamber (20) can be extended into the cold chambers (22) for imaging while remaining sealed, isolating the hot subjects from the cold imaging equipment. The imagers can thus be used for both normal clinical scanning and hot patient scanning.

Abstract: An inflatable isolating cabin is provided for a patient to be isolated, and especially for a patient to be moved or transported, and the cabin can be formed after being inflated and collapsed into a solid form convenient for storage. It comprises a very tough and soft base, a flexible outer hood, an inflatable supporting structure, and a filtering means. Wherein a part of the periphery of the outer hood is fixedly connected with the base, and the other part is detachably connected with the base; the inflatable supporting structure is provided with at least one inflation inlet hole and after the inflation of the supporting structure, the outer hood is unfolded away from the base to form the cabin to allow a patient to lie therein.

Abstract: The invention provides methods, delivery devices, and compositions for topically oxygenating hypoxic tissue with a hemoglobin-based oxygen earner (HBOC), such as Oxyglobin (Oxyb) in order to promote wound healing and/or reducing hypoxia in post-harvest transplant tissue. The invention can be used, among other things, to stimulate angiogenesis and blood flow at a wound site, reduce wound dilation, and promote wound contraction, thereby increasing the overall rate of wound healing. The invention can also be used, among other things, to reduce oxidative stress in pre-implantation donor organ tissue, as well as stimulate the proliferation of granulation tissue, vessel growth, and promote epithelial healing in transplant tissue once it has been implanted.

Abstract: The invention relates to a medical device for performing substantially bloodless surgery wherein the device comprises a double-skinned chamber with at least one through-bore.

Abstract: A hyperbaric capsule has a base forming a seat that can be enclosed by an elongate oval canopy having a large transparent window formed therein. The bottom of the front of the canopy is pivotally attached to the front of the base by a hinge assembly and can be locked in the closed position on the base by a plurality of latches that are conjointly operated by an external lever and an internal lever. The weight of the canopy upon opening is borne by a pair of side gas or spring struts.

Abstract: The interior surface of one or more walls/ceiling of the salt room is composed of inner, intermediate and outer layers. In the salt room, the salt is attached to the interior surfaces as an outer layer with an underlying intermediate layer containing salt and adhesive agent and acting as a binding agent. A binding agent is spread onto the interior surfaces of the walls of the salt room on top of the moisture insulator. Into the binding agent are embedded salt granules, after which to the binding agent surfaces containing salt granules an adhesive layer is added, which penetrates into the binding agent and attaches to the salt granules. Salt is spread on the adhesive layer as a porous coating, wherein the adhesive agent holds on to the salt layer in the binding agent surface.

Abstract: A mobile isolation unit which forms a chemical and biological barrier that is has a substantially rectangular-parallelepiped shaped enclosure and a frame system configured to support the enclosure in the suspended position so as to create and internal and external environment. The enclosure may also be equipped with at least one opening for access into and out of the enclosure, a zipper for opening and closing the access port, at least one biomedical port, and a plurality of support points configured to support the enclosed in the suspended position when the frame is in an open position so that a patient can be placed in and out of the enclosure. A method for isolating and treating a patient using the mobile isolation unit is also provided.

Abstract: A collapsible patient isolation pod for preventing flow of contaminants to or from a patient is disclosed. The isolation pod is preferably fabricated at least partially from a transparent, biochemically resistive material and includes a flexible enclosure that is configurable to receive a contaminated patient therein. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. The isolation pod has a plurality of wide, gloved access points to allow easy, multiple access points to a patient. A central connection manifold for oxygen, intravenous connections, or other fluids, may optionally be provided. Ventilation is provided within the isolation chamber with a negative pressure ventilation system and filtration on the air input near the patient's head, and provides filtration on output near the patient's feet.

Abstract: A thermotherapy device is operated as an incubator or as an open care unit. The care unit has a bed for receiving newborns, which can be closed with a hood (3). At least one heat radiation source (4) is provided. The hood (3) is located between the bed and the heat radiation source (4) when the thermotherapy device is closed and the hood is at least partially transparent to the radiation originating from the heat radiation source (4). The device allows only a small temperature drop during the transfer from the open mode of operation into the closed mode of operation and vice versa.

Abstract: An isolation enclosure is provided for isolating a person to an area about a bed, wherein the bed is adapted to support the person and includes a frame and a mattress overlying the frame. The isolation enclosure comprises a frame adapted to surround the bed; and a canopy connectable to the frame and defining an isolation chamber sealed with respect to the ambient atmosphere. The isolation chamber extends over the frame of the bed and is sufficiently large to allow a person located within the isolation chamber to be supported on the bed and to move freely within the isolation chamber. The canopy includes a base wall adapted to either (i) overly the mattress of the bed, and (ii) lie between the mattress and the frame of the bed. A frame transport device, such as wheels, casters, or sliders, is mounted on the frame and adapted to transport the frame and canopy in cooperation with the bed to thereby transport a patient supported on the bed and located within the isolation chamber.

Abstract: An isolation system with imaging or radiation therapy capability is disclosed. At least one containment barrier (14, 15, 16, 17) defines an isolation region (10). An imaging or therapy system (20) is disposed outside of the isolation region. The containment barrier includes a substantially hollow tubular extension (24, 42, 44, 124, 224, 324) protruding away from the isolation region (10). The substantially hollow tubular extension surrounds an interior volume (26) that is in fluid communication with the isolation region and is in fluid isolation from the imaging or therapy system. The substantially hollow tubular extension is made at least partially of a material providing operative communication between the imaging or therapy system and the interior volume of the substantially hollow tubular extension.

Abstract: A filter apparatus for improving gas temperature stability while maintaining a high impurity removal capacity. The filter apparatus includes a filter for removing impurities from a gas and a temperature adjuster for adjusting the temperature of the gas to a predetermined temperature. The filter apparatus further includes a humidity detector, arranged at the upstream side of the filter, for adjusting the humidity of the gas before the gas passes through the filter.

Abstract: A through-hole panel is mounted on a barrier between a hot zone maintained at a selected isolation level and a cold zone not maintained at the selected isolation level. Hermetically sealed electrical feedthroughs each include a housing and cold- and hot-side electrical receptacles, and are hermetically sealed into through-holes of the through-hole panel with the cold- and hot-side electrical receptacles extending into the respective cold and hot zones. A surface of the through-hole panel and a portion of the feedthroughs exposed to the hot zone are substantially resistant to corrosive decontamination agents used in the hot zone. A medical imaging instrument in the cold zone images an interior volume of a generally tubular imaging window that is in communication with the hot zone and is isolated from the cold zone. An auxiliary instrument in the hot zone operatively electrically communicates with the medical imaging instrument via the feedthroughs.

Abstract: A plethysmograph is constructed with a base including parallel, horizontal guide rails; an open-ended, moveable enclosure section having a horizontal central axis slidable on the guide rails between open and closed positions; a fixed enclosure section mounted on the base transverse to the horizontal pathway, the fixed enclosure section including an inner face toward the open end of the enclosure section adapted for sealing engagement with the open end of the moveable enclosure section when the moveable enclosure section is in its closed position; and a support table attached to the fixed section, the table projecting into the moveable enclosure section when the moveable enclosure section is in the closed position, the table being vertically adjustable and having an angularly adjustable longitudinal axis.

Abstract: A portable clean molding apparatus for receipt of molded articles ejected from a mold machine. The apparatus includes a receiving chamber having a first interior space and a selectively openable first door, a secondary chamber joined to the receiving chamber and having a second interior space and a selectively openable second door, and an air filtration cover unit installed over the receiving and secondary chambers so as to provide a low-particulate, positive airflow into the first and second interior spaces. The apparatus further includes at least one vent communicating with the second interior space so as to allow the airflow to exit the secondary chamber and at least one chute communicating with the first interior space so as to allow the airflow to exit the receiving chamber, the chute being located adjacent to the mold machine for the transfer of molded articles to the receiving chamber.

Abstract: The present invention relates to apparatus and systems for isolating hazardous agents and organisms from their handlers and the public. In particular, the present invention relates to modular negative pressure biological containment chambers.

Abstract: There is provided a system for protection/isolation against infections or disease-bearing persons including an enclosure defining at least two chambers, an isolation chamber having at least one entering and exiting closable opening, at least one ambient air inlet and at least one air outlet connectable to a blower/filter, and an airlock chamber juxtaposed the opening having an access and egress closable aperture, means for forming under-pressure in the isolation chamber and airlock chamber, and at least one biological filter operationally connected to the means for forming under-pressure. A method for protecting/isolating against infection or disease-bearing persons, is also provided.

Abstract: In accordance with an embodiment of the invention, an integrated air processing device includes a housing defining an air inlet, an air outlet, and a pathway from the inlet to the outlet. An air decontamination section, an air conditioning section, and a heating section are provided along the pathway. A blower is also provided along the pathway, to drive air from the inlet to the outlet, along the pathway. In another example, an integrated air processing device includes a housing as above, and an air conditioning section and a heating section along the pathway. An air decontamination section and/or a blower may also be provided along the pathway. In accordance with another embodiment, a portable isolation containment system includes one or more portable containment enclosures coupled to the integrated air processing devices described above. Methods are disclosed, as well.

Abstract: A patient care apparatus comprises a portable patient support module having a first mattress, a first platform carrying the first mattress, and a first canopy positioned on the first platform to enclose an infant positioned on the first mattress in a first isolation chamber. The portable patient support module is configured to be carried by hand when the infant is positioned on the first mattress. The patient care apparatus further comprises a second patient support module having a second mattress, a second platform carrying the second mattress, and a second canopy positioned on the second platform. The second platform and the second canopy cooperate to enclose the portable patient support module positioned on the second mattress in a second isolation chamber.

Abstract: A substance inhalation system includes a mixing flask that is in fluid communication with plural inhalation chambers. A test vapor can be selectively and individually provided to the inhalation chambers. Moreover, individual inhalation chambers can be selectively removed from the substance inhalation system without test vapor leaking from any of the inhalation chambers.

Abstract: Disclosed is a human cell/tissue culturing system including a plurality of incubators, each incubator capable of aseptically storing/culturing cell(s) or tissue(s) derived from a (human) individual and identifying the cell(s) or the tissue(s) during incubation, wherein each incubator comprises a detector corresponding to an individual key, the response of the detector permitting opening/closing of a door of each incubator, the response of the detector of one incubator triggering the interception of the function of the detector(s) of other incubator(s) to consequently inhibit opening/closing of the door(s) of the other incubator(s).

Abstract: A wound irrigation/fluid containment system having a flexible bag body defining a containment space, the bag body including walls and at least one opening with a seal, means for accessing through the bag body walls to the containment space and means for inflating portions of the walls to provide rigidity and strength to the walls. The containment device isolates a wound on a person and is capable of draining fluids away from the wound.

Abstract: The present invention relates to devices and methods for providing controlled environments for surgical procedures, as well as transplantation and wound healing. In particular, one embodiment of the present invention provides devices and methods to provide an anaerobic environment for incision sites. In other embodiments, the present invention provides devices and methods to maintain anaerobic conditions during the collection, transport, and implantation of organs, tissues, cells, and other transplant material. In further embodiments, the present invention provides devices and methods for the production and maintenance of an anaerobic environment surrounding sites of trauma or tissue injury. In particular, the present invention provides devices and methods which allow the operator to strictly control the environment for surgical procedures, transplantation and wound healing, etc. Thus, the present invention also finds use in specialized settings where hyperoxic conditions are desireable.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher. If desired, ventilation may be provided within the isolation chamber.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher. If desired, ventilation may be provided within the isolation chamber.

Abstract: A patient isolation unit including a foldable frame body, a flexible envelope made of a flammable resin sheet which can be attached to the assembled frame body, and an exhauster to discharge or exhaust the air from the envelope. The exhauster includes a UV lamp, an HEPA filter, and a blower.

Abstract: A containment and test system for extremely toxic substances includes a fume hood, a containment compartment such as glove bag or box, positioned within the fume hood, a source of a non-reactive gas to provide a stable environment within the containment compartment, an inline moisture trap coupled to the source of non-reactive gas to dry the non-reactive gas, an ion neutralizer coupled to the source of non-reactive gas to reduce static charges within the containment compartment, a staging area for preparing test samples, a balance positioned within the containment compartment, a stanchion positioned within the fume hood for holding a test animal, and decontaminating apparatus for safely disposing of any toxic substance residue.

Abstract: A self-contained transportable life support system for resuscitation, stabilization, and transport of a patient has an environmentally controlled housing for receiving and supporting a patient and a plurality of medical devices disposed within the housing. A control circuit attached to the housing has at least a portion thereof extending to an external surface of the housing for regulating operation of the medical devices and environmental conditions of within the housing in response to monitored life support conditions of the patient.

Abstract: An apparatus for isolating airborne pathogens created during a procedure performed on an individual's extremity includes a transparent, dome-shaped shield having first and second openings therein to allow two individuals to insert their respective extremities into the shield, said first and second openings being located on opposite sides of the shield, and said shield further having a ventilation opening located generally between the first and second openings; an air-cleaning filter located at the ventilation opening; and a fan mounted to the shield and communicating with the ventilation opening and the air-cleaning filter with the filter located adjacent the inlet side of the fan, whereby fumes created during the procedure are directed through the filter.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher.

Abstract: A patient care apparatus comprises a portable patient support module having a first mattress, a first platform carrying the first mattress, and a first canopy positioned on the first platform to enclose an infant positioned on the first mattress in a first isolation chamber. The portable patient support module is configured to be carried by hand when the infant is positioned on the first mattress. The patient care apparatus further comprises a second patient support module having a second mattress, a second platform carrying the second mattress, and a second canopy positioned on the second platform. The second platform and the second canopy cooperate to enclose the portable patient support module positioned on the second mattress in a second isolation chamber.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher. If desired, ventilation may be provided within the isolation chamber.

Abstract: A device for aiding in stimulating blood flow in a sexual organ of a user leading to erection. The device includes a chamber adapted to receive and enclose a user's body from adjacent the waist of the user to adjacent the upper thighs. A source of vacuum is applied to the chamber for creating a negative pressure within the chamber while permitting the user's arms to be extended into the chamber for manipulating the sexual organ.

Abstract: An examination unit having walls of substantially transparent plastic material coupled to an air tube frame that, when inflated, supports the walls to define an enclosed chamber. Access to the chamber is gained through a resealable port that facilitates easy entry and exit, as well as good sealing of the air within the chamber. Built into at least one wall of the chamber is a pair of sleeved-gloves that allow: a user of the examination unit to insert his or her hands into the chamber to handle an object therein without skin contact. The examination unit may be collapsed for space-saving storage and transport, and then readily inflated to provide a suitable environment for any number of treatments or investigations requiring that an object remain isolated from the user.

Abstract: An apparatus for isolating airborne pathogens created during a procedure performed on an individual's extremity includes a transparent, dome-shaped shield having first and second openings therein to allow two individuals to insert their respective extremities into the shield, said first and second openings being located on opposite sides of the shield, and said shield further having a ventilation opening located generally between the first and second openings; an air-cleaning filter located at the ventilation opening; and a fan mounted to the shield and communicating with the ventilation opening and the air-cleaning filter with the filter located adjacent the inlet side of the fan, whereby fumes created during the procedure are directed through the filter.

Abstract: An examination unit having walls of substantially transparent plastic material coupled to an air tube frame that, when inflated, supports the walls to define an enclosed chamber. Access to the chamber is gained through a resealable port that facilitates easy entry and exit, as well as good sealing of the air within the chamber. Built into at least one wall of the chamber is a pair of sleeved-gloves that allow a user of the examination unit to insert his or her hands into the chamber to handle an object therein without skin contact. The examination unit may be collapsed for space-saving storage and transport, and then readily inflated to provide a suitable environment for any number of treatments or investigations requiring that an object remain isolated from the user.

Abstract: The present invention relates to devices and methods for providing controlled environments for surgical procedures, as well as transplantation and wound healing. In particular, one embodiment of the present invention provides devices and methods to provide an anaerobic environment for incision sites. In other embodiments, the present invention provides devices and methods to maintain anaerobic conditions during the collection, transport, and implantation of organs, tissues, cells, and other transplant material. In further embodiments, the present invention provides devices and methods for the production and maintenance of an anaerobic environment surrounding sites of trauma or tissue injury. In particular, the present invention provides devices and methods which allow the operator to strictly control the environment for surgical procedures, transplantation and wound healing, etc. Thus, the present invention also finds use in specialized settings where hyperoxic conditions are desireable.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher. If desired, ventilation may be provided within the isolation chamber.

Abstract: An isolation chamber for providing containment for a contaminated patient includes a flexible enclosure that is configurable to receive a contaminated patient therein. The enclosure includes a first side, a second side, a top that is hingedly pivotable about a top of the first side, a bottom, a first end, and a second end. The top is maintained spaced apart from the bottom such that the top is maintained out of physical contact with a contaminated patient received in the enclosure. A plurality of attachment devices are disposed on at least one of the first and second sides or the first and second ends. The plurality of attachment devices are configured to attach to one of the first and second sides or the first and second ends to support members of a stretcher.

Abstract: In a lighting system capable of varying luminance of the light emitting surface periodically used for adjusting rhythm of breathing of an observer when he wishes to fall asleep, a light source is controlled in a manner so that variation of the luminance “L” per a unit time in the vicinity at a time tMAX when the luminance “L” takes the largest value in one period becomes larger than the variation of the luminance “L” per the unit time in the vicinity at a time tMIN when the luminance “L” takes the smallest value.

Abstract: A multisensory stimulation system and method of use. The system includes a housing articulate on a support so as to align a marked viewport with an individual. The housing defines a viewing chamber which is an extension of a reflective light and image optical system chamber which receives light and images from one or more video monitors or images projectors and, in some embodiments, from alternate sources such as black lights and strobe light devices. The system also includes an aromatic sensory component, tactile sensation devices, an audio input system, and audio delivery devices.

Abstract: The present invention relates to devices and methods for providing controlled environments for surgical procedures, as well as transplantation and wound healing. In particular, one embodiment of the present invention provides devices and methods to provide an anaerobic environment for incision sites. In other embodiments, the present invention provides devices and methods to maintain anaerobic conditions during the collection, transport, and implantation of organs, tissues, cells, and other transplant material. In further embodiments, the present invention provides devices and methods for the production and maintenance of an anaerobic environment surrounding sites of trauma or tissue injury. In particular, the present invention provides devices and methods which allow the operator to strictly control the environment for surgical procedures, transplantation and wound healing, etc. Thus, the present invention also finds use in specialized settings where hyperoxic conditions are desireable.

Abstract: The present invention relates to a multifunction hyperthermo-therapeutical apparatus, and more particularly, to a multifunction hyperthermo-therapeutical apparatus which basically uses the hyperthermo-therapeutical apparatus and, of course, selectively uses one or more specific appliances according to the selection of a user by installing a sleep aid means, foot pressure means and vertebral correction means with additional functions at the one hyperthermo-therapeutical apparatus, thereby maximizing a hyperthermo-therapeutical curative effect and achieving an optimum sleep, blood circulation and vertebral correction.

Abstract: An infant apparatus having a base, a vertically movable hood and a plurality of walls that form an infant compartment. The apparatus has lateral side walls and a front end door that can be individually opened. There is an interlocking engagement between the upper periphery of the lateral walls and hood by a plurality of pins on the hood that engage brackets located at the top of the front and rear end walls. A latching arrangement allows all three doors to be opened. The side lateral doors are latched by a movable latch member that enters an opening in brackets affixed to the front and rear end walls. The front end wall can be moved vertically upwardly to disengage its latching arrangement to enable it to pivot downwardly. An alignment mechanism is also provided to insure that the movable latch members correctly align with the openings in the brackets.

Abstract: A modulator transportable collective protection system for the decontamination and containment of personnel in a toxic free area. A contamination containment area is provided through which personnel are decontaminated prior to entering the toxic free area. The migration of contaminants is prevented by causing a purge of clean filtered air from the toxic free area to the contamination control area and to the exterior environment. A blower and filter unit provides air to the toxic free area to maintain an over pressure therein, ensuring that all entry to the toxic free area is through a flow of clean air.

Abstract: A system for providing clean air environments for sleeping, resting, working or exercising in order to provide relieve and therapeutic benefits to people with bronchial asthma and respiratory allergies, such system comprising of a tent or stationary enclosure, an air-pumping device and a HEPA filter that removes dust, bacteria and allergens from air entering tent or enclosure; the air-pumping device can be installed in two different configurations: in air-supply or air-removal mode, in both providing necessary ventilation and supply of clean air for breathing.

Abstract: A modulator transportable collective protection system for the decontamination and containment of personnel in a toxic free area. A contamination containment area is provided through which personnel are decontaminated prior to entering the toxic free area. The migration of contaminants is prevented by causing a purge of clean filtered air from the toxic free area to the contamination control area and to the exterior environment. A blower and filter unit provides air to the toxic free area to maintain an over pressure therein, ensuring that all entry to the toxic free area is through a flow of clean air.

Abstract: A modulator transportable collective protection system for the decontamination and containment of personnel in a toxic free area. A contamination containment area is provided through which personnel are decontaminated prior to entering the toxic free area. The migration of contaminants is prevented by causing a purge of clean filtered air from the toxic free area to the contamination control area and to the exterior environment. A blower and filter unit provides air to the toxic free area to maintain an over pressure therein, ensuring that all entry to the toxic free area is through a flow of clean air.

Abstract: A modulator transportable collective protection system for the decontamination and containment of personnel in a toxic free area. A contamination containment area is provided through which personnel are decontaminated prior to entering the toxic free area. The migration of contaminants is prevented by causing a purge of clean filtered air from the toxic free area to the contamination control area and to the exterior environment. A blower and filter unit provides air to the toxic free area to maintain an over pressure therein, ensuring that all entry to the toxic free area is through a flow of clean air.