MedEq Fitness
TimePod 2 Single-Person 2.0 ATA Triangular Hard-Shell Hyperbaric Chamber
TimePod 2 Single-Person 2.0 ATA Triangular Hard-Shell Hyperbaric Chamber
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Plan a single-occupant chamber installation with the TimePod 2's triangular hard-shell format. Listed viewing areas and internal/external interfaces support an operator-managed setup, while a separate integrated host console brings air, oxygen and climate functions together. Confirm the delivered configuration, medical suitability and site requirements before ordering.
Why Customers Choose This Product
- Triangular single-occupant chamber format.
- Listed nickel-steel alloy shell with powder-coated exterior.
- Transparent door/viewing areas.
- Internal and external interfaces, configuration-dependent.
- Integrated host console for air, oxygen and climate functions.
- White, Black, Blue, Gray and Silver selections.
Product Highlights
Triangular layout
The source describes a triangular hard-shell chamber for one adult. Plan placement using a confirmed dimensional drawing and service clearances, not an assumed space-saving comparison.
Listed pressure range
The listing states 1.3 to 2.0 ATA, with configuration references at 1.3, 1.5, 1.7 and 2.0 ATA. These are equipment specifications, not recommended treatment pressures or session instructions.
Integrated host functions
The source describes an air compressor and PSA oxygen generation with configuration-dependent cooling and dehumidification. Confirm component models, operating ratings and approved oxygen-delivery arrangements in the build sheet.
Viewing and monitoring
Transparent viewing areas accompany internal gauges and external host displays. Available sensors, emergency-stop functions and interfaces vary by model and require confirmation.
Specifications
- Product: TimePod 2
- Vendor: MedEq Fitness
- Manufacturer identified in source: OxyPrime/OxyRevo; confirm exact supplied model
- Type: triangular hard-shell hyperbaric chamber
- Occupancy: one adult, subject to confirmed fit and load limits
- Listed pressure range: 1.3 to 2.0 ATA; configuration references at 1.3, 1.5, 1.7 and 2.0 ATA
- Approximate external dimensions: 200 cm long by 87 cm wide by 153 cm high
- Rounded imperial dimensions in source: 79 by 34 by 60 in
- Listed chamber weight: 600 kg; component scope and total installed weight require confirmation
- Listed occupied floor area: approximately 1.62 m²; measurement basis and required service area not supplied
- Shell: nickel-steel alloy with powder-coated exterior, as listed
- Interior finishes: composite/TPU-based, as listed
- Door: source conflicts between modified sliding and lift-up designs; confirm delivered mechanism
- Host: integrated air compressor, PSA oxygen generation and configuration-dependent climate/air-handling functions
- Example oxygen-flow reference: 10 to 15 L/min; not a verified delivered rating
- Supplier-listed oxygen-outlet concentration: at least 90 percent, configuration-dependent; flow/test conditions not supplied; not chamber oxygen concentration
- Relief features listed: automatic and manual pressure-relief valves
- Interfaces: internal/external controls and emergency-stop functions, model-dependent
- Monitoring: internal pressure gauges and host displays; oxygen, temperature and humidity displays depend on configuration
- Mobility: base castors listed
- Noise reference: target of 50 dB or less; not a verified operating guarantee
- Power configurations: AC 110 V / 60 Hz or 220 V / 50 Hz, model-dependent; not universal-voltage operation
- Optional items described: BIBS oxygen delivery, internal light panel, interior finishes and exterior customization; confirm availability and compatibility separately
- Color selections: White, Black, Blue, Gray and Silver
- Listed limited warranty: two years for chamber shell/frame/door, subject to written terms; host, electronics and accessories have separately specified coverage
Ideal For
Buyers planning a professionally assessed single-person installation where intended use is permitted and supported by qualified medical evaluation, appropriate facilities, trained operators and supervision. The listing does not establish clinical approval, pediatric suitability or suitability for unsupervised home use.
Important Information
Hyperbaric pressure and supplemental oxygen carry serious risks, including pressure injury and fire. Obtain assessment from a clinician qualified in hyperbaric medicine and follow the documented intended use, contraindications and operating limits. Do not choose pressure, oxygen flow or session duration from this sales description. Obtain model-specific regulatory and pressure-vessel documentation and confirm prescription, facility, inspection and operator requirements. No FDA clearance, aviation-grade status or medical-grade approval is established by this listing.
Arrange qualified installation, training, commissioning and supervision with documented monitoring, communication, depressurization and emergency procedures. Do not operate alone, bypass interlocks or open the door while pressurized. Follow the approved procedure for returning to ambient pressure and exiting. Confirm whether the delivered door slides or lifts before planning access and overhead clearance.
Keep smoking, flames, sparks and ignition sources away. Use only manufacturer-approved oxygen delivery, electrical equipment, clothing, accessories and cleaning products for this exact chamber. Do not introduce unapproved electronics, oils or combustible materials. Confirm ventilation, oxygen monitoring, fire precautions and emissions documentation for any ionization/disinfection module. No microbial reduction, non-toxic coating or air-purification performance is promised here. Do not pressurize the chamber with oxygen unless explicitly authorized by the manufacturer and applicable requirements.
BIBS and internal light equipment are described as optional, not included. Do not install or operate an internal light panel without explicit model-specific approval for the pressurized and oxygen-related environment. Example wavelength and oxygen-flow references in the source do not establish the supplied equipment's specifications. Concentrator outlet purity does not establish chamber atmosphere or delivered exposure.
Obtain confirmed drawings and a build sheet covering occupant limits, total weight, host dimensions, electrical load, door mechanism and component ratings. The stated floor area does not establish the full room footprint including equipment and clearances. Have qualified professionals assess floor support, lifting, delivery paths and service access. Castors do not establish safe movement while occupied or pressurized. Confirm written warranty and freight/installation terms, follow model-specific maintenance and calibration instructions, and remove damaged or malfunctioning equipment from service.
Frequently Asked Questions
How many people is the TimePod 2 designed for?
The source identifies a single adult occupant. Confirm usable interior dimensions, supported user size and maximum load before purchase.
What pressure range is listed?
The source states 1.3 to 2.0 ATA, with configuration references at 1.3, 1.5, 1.7 and 2.0 ATA. Confirm the supplied configuration; these values are not treatment recommendations.
Does the door slide or lift?
The source describes both a modified sliding door and a lift-up door. Obtain confirmation of the delivered mechanism and its required clearances.
Are BIBS and the internal light panel included?
No standard inclusion is established. Both are described as optional; confirm availability, exact specifications and manufacturer approval for the supplied chamber before adding them.
What electrical configuration is listed?
The source lists AC 110 V / 60 Hz or 220 V / 50 Hz depending on model. Confirm the delivered ratings, plug type and electrical load before installation.
If the triangular single-person format fits your professionally assessed requirements, confirm the build sheet, documentation and installation plan before choosing your color and ordering.
No treatment or health outcomes are promised. Hyperbaric pressure and oxygen require qualified medical assessment, appropriate training and manufacturer-directed operation. This description is not medical advice.