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HPO TEC MATRIX 1 Multiplace Hyperbaric Chamber

by Hpo Tec
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MATRIX - Futuristic Cube-Design Hyperbaric Chamber for 1 and 2 Seats

The new-generation MATRIX hyperbaric chamber blends sleek, futuristic design with rock-solid engineering. Built with heavy-duty steel and rounded corners that add a touch of style, this powerhouse hyperbaric chamber can reach an impressive 3.0 ATA pressure. The cube shape maximizes interior space, creating a generous 5.8 m3 environment for hyperbaric oxygen therapy sessions. Automatic operation guarantees simplicity and convenience, making the therapy experience user-friendly, effective, and most of all, enjoyable. The MATRIX technological platform can extend occupancy to 2 persons and allow for wheelchair access, making it one of the most versatile and accessible hyperbaric chamber systems available.

MATRIX is designed to turn every hyperbaric oxygen therapy session into a relaxing, memorable experience. Inside, high-quality ecologic leather upholstery with customizable colors, stitch designs, and embroidery options creates a comfortable and inviting environment. Ergonomic seating - with a choice of 3 models including the luxury electric Maybach chair range - reduces pressure point stress and boosts circulation throughout every session. Adjustable LED RGB lights, an entertainment system, and an advanced air cooling system complete the experience. For clinical and wellness facilities, MATRIX's centralized software control, real-time session monitoring, and full automation system give operators complete oversight and clinical-grade performance from a compact, cube-shaped platform.


Specifications

General
Capacity 1 Person (1 seat) / 2 Persons (2 seats - optional)
Material Steel pressure vessel
Shape and Design 2 module cube shape, designed to fit any standard doorway and space
Module Length 770 mm
Maximum Patient Weight 225 kg per patient
Dimensions
Overall Length 1750 mm
Overall Width 1442 mm
Height 1793 mm
Internal Length 1731 mm
Internal Volume 5.8 m3
Weight 1550 kg
Minimum Installation Floor Size 4500 mm x 300 mm (as listed on source - please verify)
Operating Conditions
Max. Operating Pressure 2.0 ATA (1.0 BAR)
Design Temperature 0 degrees C to 38 degrees C
Emergency Depressurization Rate 2.0 ATA to 1.0 ATA in 90 sec
Air Systems
Air Pressurization 3.45 bar to 7.2 bar
Air Supply Flow 250 LPM
Ventilation Rate 150 LPM
Oxygen Supply
BIBS Oxygen Supply 3.2 bar to 4.0 bar

Oxygen Concentrator Specifications

Performance - 4 Units (1 per seat)
Power 2500 W / 3.3 HP
Oxygen Flow Range 1 to 20 LPM
Oxygen Output Pressure 5 BAR / 72 PSI
Oxygen Purity +-93%
Noise Level <= 72 dB
Weight 155 kg
Dimensions
Length 695 mm
Width 481 mm
Height 1070 mm

Air Compressor Specifications

Performance - 1 Unit
Power 4 HP
Pressure Range 1 to 8 bar (116 psi)
Airflow Capacity 564 LPM
Noise Level 46 decibels
Weight 67 kg
Dimensions
Width 495 mm
Length 1004 mm
Height 804 mm

Air Cooler Specifications

Performance - 1 Unit
Cooling Capacity 1 kW (at -10 degrees C)
Temperature Stability +-0.1 degrees C
Set Temperature Range -10 degrees C to 40 degrees C
Cooling Method Air-cooled refrigeration
Dimensions
Width 377 mm
Length 500 mm
Height 640 mm

Features

BIBS Mask

The Built-In Breathing System (BIBS) is regulated by the tempo of your breath. The BIBS regulator circulates oxygen effectively through the polyurethane hose while removing carbon dioxide, ensuring a safe and controlled therapy environment with always-pure oxygen breathing.

Continuous Flow of Oxygen

Unlike demand regulators, BIBS systems provide a constant flow of oxygen regardless of breathing patterns. This is beneficial for patients who struggle with deep breaths or have conditions affecting their respiratory muscles.

Reduced Risk of CO2 Buildup

The system constantly flushes the chamber with fresh oxygen, helping prevent the buildup of carbon dioxide, which can be harmful at high pressures.

Simplified Operation

BIBS systems require minimal interaction from the user, making them easier to use for patients with limited mobility or cognitive abilities.

Controlled Oxygen Concentration

The flow rate of oxygen can be precisely adjusted to deliver the desired concentration, even if the pressure inside the chamber fluctuates.

External Control Panel

Navigate pressure adjustments, monitor vital information, maintain clear communication with your patient, and control every aspect of the chamber with confidence. Be prepared for any situation with manual overrides and an emergency stop button.

External Control Tablet

Manage everything with the intuitive touchscreen control, from setting the pressure and session parameters to locking the chamber door. Monitor the session with clear visuals and data on chamber pressure, time, and other vital information.

Manual Compression / Decompression Knob

Take command with the manual pressure knobs, adjusting compression and decompression independently of the automatic system for greater control over any phase of the session.

Power On Switch

The switch turns on the electrical equipment, activating the control panels for manual and/or automatic HBOT sessions.

Emergency Decompression Valve

In case of emergency, the pressure chamber is relieved by rotating the manual spherical valve from inside or outside the chamber, providing a physical backup to all software controls.

Emergency Stop Button

Terminates the session in the pressure room if needed and quickly drops chamber pressure to a safe level. Available on both external and internal control panels.

External Intercom

Provides voice connection with the user inside the chamber. Always open for crystal clear communication with volume control, ensuring continuous contact throughout the session.

USB Port

The USB 3.0 port allows software updates, uploading custom settings, or downloading the session archive for record-keeping and clinical review.

Internal Control Panel

Take charge of your hyperbaric experience with the intuitive internal control panel. Adjust pressure, time, and settings, all while monitoring key information on the built-in displays. All commands are mirrored for outside and inside user control.

Internal Control Tablet

Manage everything from within the chamber with the intuitive touchscreen, from setting pressure and session parameters to monitoring all vital information during treatment.

Chamber Pressure Indicator

A mechanical dial indicator provides a quick analog reading of pressure variations inside the chamber, giving the patient an instant visual reference at all times.

Internal Cooler

Operated using the control tablet, the internal cooler adjusts chamber temperature when pressurized, maintaining a comfortable HBOT session experience throughout.

Internal Intercom

Provides voice communication with outside operators. Always open for crystal clear communication, ensuring the patient is never isolated during treatment.

UV-C Light Disinfection

The chamber features UV-C light disinfection that inactivates viruses and bacteria from surfaces and ambient air, keeping the interior environment clean and safe between sessions.

Occupancy Sensor

Automatically disables UV-C when someone enters the pressure chamber, ensuring disinfection operates only when the chamber is unoccupied and safe to run.

Centralized Software Control

The control consoles, located on the outside and inside the chamber, provide the controls and instrumentation for chamber operation. The user-friendly interface allows customization of specific HBOT protocols with accurate metrics and simple controls.

Real-Time Session Monitoring

Sensors track essential parameters during HBOT sessions, enabling real-time monitoring and adjustments. The system gathers and displays real-time session information including pressure, oxygen, temperature, humidity, patient vitals, and treatment duration.

Session Status Management

The protocols of each HBOT session are recorded in the data logger for future reference. This enables healthcare providers to observe treatment response, adjust protocols if necessary, and assess the overall progress of the therapy.

Advanced Automation System

The chamber is fully automated via an advanced Automation System consisting of automation software, industrial PLC, sensors, valves, and a PC. The PLC is the central control unit, monitoring and controlling all connected devices to streamline chamber operations and reduce manual intervention.

Ergonomic Seating

Tailored to your body's physiology, the ergonomic seats reduce pressure point stress and boost circulation, ensuring a relaxed and effective session. Choose between 3 ergonomic chair models with automatic or manual controls, including the luxury electric Maybach chair range with full customization options.

Optional Wheelchair Access

What truly sets the MATRIX apart is accessibility. With an electrical door and an automatic ramp, it ensures easy wheelchair access. Its spacious interior can accommodate two people, with the flexibility to host up to three, making it ideal for families or advanced therapy needs requiring assistants.

Interior Leather

The interior is wrapped in high-quality ecologic leather upholstery for the most comfortable and inviting feeling, with a classy look. Choose your favorite leather color, stitch color, stitch design, or embroidery options for a fully personalized interior.

Patient Monitoring

Chamber penetrations and electrical connectors provide the capability to connect vital monitoring equipment such as EEG, ECG, TCOM, and blood pressure devices.

Entertainment System

The chamber is equipped with large-screen TV or tablets for the users, including other customizable additions to improve the in-chamber experience.

Adjustable LED RGB Lighting

Adjustable LED RGB lighting allows you to create a serene and personalized atmosphere inside the chamber during each session.

Ventilation

The automatic ventilation system ensures the air inside the chamber is always fresh throughout the duration of every session.

Pneumatic Controls

Chamber controls are completely pneumatic in nature and require only a compressed gas source, keeping operation clean and reliable.

Discrete Power Source

A discrete power source allows continued operation of chamber communications in the event of a power outage, maintaining safety and connectivity at all times.


Certifications

CE Mark
93/42/EEC - Medical Devices Directive (MDD)

This European Union directive ensures that HPO TECH hyperbaric chambers meet essential safety and performance requirements for medical devices. Compliance with MDD guarantees that the chambers are suitable for therapeutic use within healthcare settings.

MDR 2017/745
Medical Devices Directive (MDR)

The company has transitioned from the MDD certification to the new MDR framework, aligning with the latest EU medical device regulations for enhanced safety and performance standards.

UKCA
UKCA - UK Conformity Assessed

Confirms chambers meet post-Brexit UK regulatory requirements for medical devices, ensuring compliance with safety, performance, and environmental protection standards.

ASME PVHO
ASME PVHO - Pressure Vessels for Human Occupancy

ASME standard ensuring chambers are designed and built to safely accommodate human occupants under pressurized conditions, reducing risks associated with high-pressure environments.

ASME U-Stamp
ASME U-Stamp

ASME certification confirming the pressure vessel complies with strict safety, design, fabrication, and testing standards under Section VIII, Division 1 of the BPVC.

PED
PED - Pressure Equipment Directive

European standard regulating the design, manufacturing, and testing of pressurized equipment, ensuring hyperbaric chambers can safely handle the pressures required for hyperbaric therapy.

ISO 13485
ISO 13485 - Medical Devices Quality Management System

Confirms adherence to internationally recognized standards for medical device manufacturing and quality control throughout the product lifecycle.

ISO 45001
ISO 45001 - Occupational Health and Safety Management System

Ensures chambers are manufactured under a management system that prioritizes employee safety and health in the workplace.

ISO 9001
ISO 9001 - Quality Management System

Covers mechanical safety of hyperbaric chambers including moving parts, emergency stops, and user interfaces to protect operators and patients.

ISO 14001
ISO 14001 - Environmental Management System

Confirms the company follows environmental best practices in its manufacturing processes, reducing ecological impact and ensuring sustainability.

ISO 27001
ISO 27001 - Information Security Management System

Ensures protection of sensitive patient and operational data through strict information security management protocols.

2001/95/EC
2001/95/EC - General Product Safety Directive

EU directive setting general safety requirements for products placed on the EU market, complementing the CE marking under MDR.

Turk Lloydu
Turk Lloydu - Hydrostatic Testing and Conformity Assessment

Certification for pressure testing and structural integrity of hyperbaric chambers, verifying safety and compliance with international hydrostatic standards.

NFPA
NFPA - National Fire Protection Association (USA)

Establishes fire safety guidelines for hyperbaric chambers, ensuring compliance with strict fire prevention and suppression standards in medical environments.

ANEP 26
ANEP 26 - Ergonomic Military Standards

Ergonomic standard establishing general human engineering design criteria for military systems, subsystems, equipment, and facilities.

Medsafe New Zealand
Medsafe, New Zealand

New Zealand's medical device regulatory body ensures HPO TECH chambers meet national healthcare standards for safety and effectiveness.

Thai FDA
Thai FDA - Thailand

Ensures chambers meet strict safety and performance standards before legal sale in Thailand, signifying full regulatory compliance.

FDA Ghana
FDA - Ghana

Ghana FDA certification supporting healthcare, wellness, recovery, and human performance across Africa.

Saudi FDA SFDA
Saudi Food and Drug Authority (SFDA)

Certified as medical devices by the SFDA with full marketing authorization in the Kingdom of Saudi Arabia.

UAE Ministry of Health
UAE - Ministry of Health

Certified by both the UAE Ministry of Health and Prevention (MOHAP) and the Emirates Drug and Medical Devices Regulation Agency (EDE), affirming compliance with UAE medical and technical standards.

UAE EDE
UAE - Emirates Drug and Medical Devices Regulation Agency (EDE)

Dual certification with MOHAP confirming compliance with UAE regulatory requirements for medical device safety, quality, and clinical performance across hospitals and clinics throughout the Emirates.

Patents
Patents

All chamber models are protected by design and utility model patents registered with Turk Patent and recognized internationally through the WIPO Hague System, covering Turkey, the EU, and the USA.


Frequently asked questions

What distinguishes the HPOTECH Matrix 2 in the multiplace lineup?
The HPOTECH Matrix 2 is a hard-shell, steel pressure-vessel chamber built for two-occupant, multiplace sessions at 2.0-3.0 ATA, certified to ASME PVHO/U-Stamp and CE PED pressure-vessel standards. Unlike single-occupant monoplace models, it pressurizes multiple people together in one cabin - a fit for clinical, hospital, hospitality, and wellness operators that need verified multi-occupant performance.
Which facility types is the Matrix 2 multiplace chamber designed to support?
The Matrix 2 multiplace chamber is designed for clinical, hospital, hospitality, and wellness operators running multi-occupant sessions instead of single-user therapy. Its two-seat, hard-shell cabin pressurizes two occupants together at 2.0-3.0 ATA in one shared session, suited to facilities that prioritize simultaneous multi-person capacity over one-person-at-a-time throughput when choosing equipment.
What pressure range does the Matrix 2 operate at?
The HPOTECH Matrix 2 operates at 2.0-3.0 ATA, a hyperbaric pressure range delivered inside a two-seat, steel hard-shell pressure vessel weighing approximately 1,550 kg. This multiplace envelope holds two occupants at the same calibrated pressure at once, unlike single-seat monoplace units which pressurize one person per session.
What site requirements does installing a Matrix 2 multiplace chamber involve?
A HPOTECH Matrix 2 installation requires a structured site-readiness review: electrical supply capacity and dedicated-circuit sizing for the pressure system, floor-load verification sized to the vessel's roughly 1,550 kg installed weight, and crane access to deliver and position the two-seat, steel hard-shell pressure vessel into place.
What does post-installation support from HPOTECH cover for Matrix 2 owners?
Post-installation support for Matrix 2 owners covers pressure-system calibration, door-mechanism service, and safety redundancy checks under a structured service plan. The plan also includes operator refresher training so staff stay current on safe operating procedure for the two-seat, multiplace chamber.

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You will be charged a 20% restocking fee, and you will pay for the return freight.
You are eligible for a full refund if the return is because of an error by the manufacturer (Merits Healthcare).
If an order is canceled after the item has shipped the standard return policy applies with a 20% restocking fee. You should accept delivery of the item(s), obtain an RA number, and ship the item(s) back. You will pay for the return freight.
If the item is damaged during shipment please call MEDIRISER Customer Service at 251-292-1169.
Unfortunately, delivery service fees, including White Glove Delivery, and Tech Set-Up are not refundable.

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