Systems and methods are provided for managing medical devices. In one embodiment, medical device usage data is stored on the medical device to indicate the usage, health, and alarm or error codes. The usage data is electronically read and assessed against one or more thresholds to determine if the medical device is operating properly and, hence, can be inventoried for reuse, or is need of service or repair. Other embodiments are also disclosed wherein the medical device wirelessly scan its environment to ensure, for example, the device is used with approved accessories or components and personnel. In yet other embodiments, medical devices are provided that can configure themselves for operation by scanning any connected components for component-specific operational data. The operational data is then used to configure the medical device to operate with the component.

Systems and methods are provided that obtain the same or better level of performance by using lower operating flow rates, pressures and/or optimized flow distributions within the system. This extends the life of system components and lower energy consumption. In one embodiment, gas separation (or sieve) beds that are used to separate gaseous components are provided that have lower flow and pressure requirements compared to conventional beds. The sieve beds include, for example, a diffuser having low solid area in cross-section and maximum open area for flow while providing adequate mechanical properties to contain sieve material and support filter media. In another embodiment, systems and methods are provided having an indicator when a component has been serviced or repaired. This provides an indication whether the component has been tampered with in any manner. This allows the manufacturer to determine if the component was serviced, repaired, or tampered with outside the manufacturer's domain.

Systems and methods are provided that obtain the same or better level of performance by using lower operating flow rates, pressures and/or optimized flow distributions within the system. This extends the life of system components and lower energy consumption. In one embodiment, gas separation (or sieve) beds that are used to separate gaseous components are provided that have lower flow and pressure requirements compared to conventional beds. The sieve beds include, for example, a diffuser having low solid area in cross-section and maximum open area for flow while providing adequate mechanical properties to contain sieve material and support filter media. In another embodiment, systems and methods are provided having an indicator when a component has been serviced or repaired. This provides an indication whether the component has been tampered with in any manner. This allows the manufacturer to determine if the component was serviced, repaired, or tampered with outside the manufacturer's domain.

According to some embodiments, a protective face mask to protect medical personnel by filtering exhaled air of infectious patients is disclosed. The protective face mask comprises a first layer, a second layer and a third layer. The second layer comprises a molecular sieve desiccant. The molecular sieve desiccant is between 0.1 cm and 10 cm thick.

Disclosed is a method and device for inactivating or killing airborne bacteria, fungi, molds and viruses by passing the air through a filter material formed of a fabric having particles of zinc disposed in discrete physically isolated locations, wherein the particles of zinc and oxygen from the air form half cells of a battery whereby to create an electrical field that inactivates or kills airborne bacteria, fungi, molds and viruses passing through the filter material.

A cartridge for applying an electromagnetic field (EMF) to at least one toxin in a wound in the skin of a person or animal is provided. The cartridge includes a power supply, a controller coupled to the power supply and providing a voltage between about 0.2V and 3V to an array of electrodes configured to transmit the EMF to the skin about the wound site. A cartridge for applying an ultrasonic field to at least one toxin in a wound in the skin of a person or animal is also provided. The ultrasonic cartridge may include a power supply, a controller coupled to the power supply and providing a voltage to at least one sonotrodes configured to transmit the ultrasonic field to the skin about the wound. The cartridge may also include a sensor for measuring the resistance or impedance in the tissue to be treated and the controller can adjust the ultrasonic field based on the impedance or resistance.

The present invention discloses a sack comprising a second container and a first container, an activated carbon filter that is positioned between said first and second containers and a sealable rubberized zipper and the activated carbon filter is positioned such that it may absorb at least a portion of odor and moisture from items stored inside sack. In addition, an antimicrobial material may be infused into the material of the sack.

A protective face mask may comprise an outer housing including a first plurality of ventilation holes, and an inner housing detachably coupled to the outer housing, the inner housing configured to cover a nose and a mouth of a user, the inner housing including a second plurality of ventilation holes. The protective face mask may also include a replaceable filter configured to be received in a space between the inner housing and the outer housing. In some embodiments, the protective face mask includes a sensor unit coupled to at least one of the inner housing and the outer housing, the sensor unit configured to detect a presence of a contaminant on the replaceable filter.

An air treatment system for at least partially removing at least one gaseous contaminant contained in indoor air of a room structured for human occupants. The system may comprise an air treatment assembly having an indoor air inlet configured to receive indoor airflow directly from a room, a regenerable adsorbent material configured to adsorb at least one gaseous contaminant contained in the indoor airflow, at least one airflow element for directing the indoor airflow to flow through the air treatment assembly, an indoor air outlet for expelling the indoor air, from the air treatment assembly back into the room, a purge air inlet configured to receive and direct purge air over and/or through the adsorbent material for removal of at least a portion of the at least one gaseous contaminant, and a purge air outlet for expelling the purge air out of the air treatment assembly.

A portable breathing apparatus for oxygen enrichment of breathable air comprises: an adsorption vessel; an air compressor for pumping air into the adsorption vessel; a valve for purging pressure from the adsorption vessel; an adsorbent disposed within the adsorption vessel adsorbing a non-oxygen constituent of air when the vessel is pressurized, thereby producing oxygen-enriched air, and desorbing the non-oxygen constituent when the pressure is purged.