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HPO TEC TITAN OMEGA Monoplace Hyperbaric Chamber

by Hpo Tec
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TITAN OMEGA - Large Multiplace Hyperbaric Chamber for Medical Applications

The TITAN OMEGA is HPO TECH's largest and most powerful hyperbaric chamber system, featuring a distinctive omega-shaped cylindrical exterior and purpose-built for hospitals, large HBOT clinics, and high-throughput medical facilities. Accommodating up to 12+2 seats (14 occupants), TITAN OMEGA operates across a wide pressure range of 3.0 to 6.0 ATA, providing the clinical flexibility to run both standard and high-pressure multiplace protocols in a single certified system. Manufactured from steel with a modular cylindrical construction, TITAN OMEGA is built for the rigors of intensive, high-volume clinical use while maintaining a safe and comfortable environment for every patient. Efficient pure oxygen delivery via the BIBS mask, advanced real-time monitoring, and a comprehensive automation system ensure that clinical teams have full visibility and control throughout every session.

TITAN OMEGA delivers user-centric design and leading-edge technology in a fully automatic and manual multiplace hyperbaric chamber system designed and certified for medical applications. The system includes a fully automated control panel, multi-angle video camera monitoring, integrated fire suppression, and extensive customization options covering seating configuration (4+2 up to 12+2), brandable ergonomic seats, brandable interior and exterior design, RGB LED lighting, entertainment systems, and custom 3D epoxy flooring. Every TITAN OMEGA installation is preceded by a site-readiness review covering floor loading, access routes, electrical capacity, and technical room planning before commissioning begins.


Specifications

General
Capacity 4+2, 6+2, 8+2, 10+2, 12+2 patients (up to 14 seats)
Material Steel
Shape and Design Omega-shaped cylindrical exterior, modular, designed to fit any standard doorway and space
Maximum Patient Weight 225 kg per patient
Dimensions
Overall Length 7988 mm
Overall Width 2356 mm
Height 2604 mm
Internal Diameter 2200 mm
Module Length 770 mm
Min. Floor Size - Technical Room 9000 mm x 6200 mm (compressor, dryer, air tanks)
Min. Floor Size - Chamber Room 13000 mm x 6000 mm (chamber and fire system)
Operating Conditions
Max. Operating Pressure 3.0 ATA to 6.0 ATA (5.0 bar)
Maximum Design Overpressure 5.5 bar
Testing Overpressure 8.25 bar
Design Temperature 0 degrees C to 38 degrees C
Emergency Depressurization Rate 3 ATA to 1 ATA in 125 sec
Air and Oxygen Systems
Air Supply Flow 450 LPM
BIBS Oxygen Supply 5 bar / 40 LPM flow
Ventilation Rate 600 LPM

Air Compressor Specifications

Ozen Kompresor - 3 Units
Motor Power 110 kW / 150 HP
Working Pressure 75 / 10 / 13 bar
Capacity (FAD) 19.57 / 17.1 / 14.68 m3/min
Noise Level 76 dB(A)
Connection Diameter 2 inch
Weight 2650 to 2740 kg
Dimensions
Width 1700 mm
Length 2700 mm
Height 1855 mm

Air Stock Tanks

4 Units
Height 2140 mm
Width 1000 mm
Distance Between Tanks 657 mm

Control Panel

1 Unit - Dimensions
Height 1652 mm
Width 1490 mm
Depth 1160 mm

Fire Suppression System

1000 L Main Water Tank - 5 Units
Height 1895 mm
Width 750 mm
500 L Antechamber Water Tank
Height 1395 mm
Width 750 mm
High-Pressure Nitrogen Cylinders - 3 Units
Height 1456 mm
Width 230 mm

Features

BIBS Mask

During treatment, each patient breathes high-purity oxygen directly from the BIBS mask. 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. Oxygen is supplied from the medical facility's oxygen tanks.

External Control Panel

The command center for the hyperbaric session. Navigate pressure adjustments, monitor vital information, maintain clear communication with patients, and control every aspect of the chamber with confidence. Manual overrides and an emergency stop button are always available.

Control Screen

A built-in mini-computer manages everything from setting pressure and session parameters to locking the chamber door. Monitor sessions with clear visuals and data on chamber pressure, time, and all vital information in real time.

Video Camera Monitoring

Multiple interior cameras cover all angles inside the chamber, monitoring each patient's response to hyperbaric oxygen therapy. Video is broadcast live on the control panel, providing the operator with full visual oversight throughout every session.

External Intercom

Provides voice connection with users and assistants inside the chamber. Always open for crystal clear communication with volume control, ensuring continuous contact between the operator and all occupants.

Manual Compression Knob

Provides manual control over compression independently of the automatic system, giving the operator greater precision over pressure adjustments during any phase of the session.

Manual Decompression Knob

Provides manual control over decompression independently of the automatic system, giving the operator greater precision and safety oversight during the decompression phase.

Emergency Stop Button

Terminates the session in the pressure room if needed and quickly drops chamber pressure to a safe level, providing immediate safety response for any clinical situation.

Power On Switch

Turns on all electrical equipment, activating the control panels for manual and/or automatic HBOT sessions with a single action.

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 automated controls.

Fire Suppression System

The integrated fire suppression system is used to extinguish, control, or entirely prevent fires from spreading or occurring. It comprises a main 1000 L water stock tank, a 500 L antechamber tank, and 3 high-pressure nitrogen cylinders, ensuring the highest level of safety in a high-oxygen clinical environment.

Air Generating Unit

Three industrial air compressors (Ozen Kompresor, 110 kW / 150 HP each) pressurize the chamber with breathable air. Air is circulated through the air dryer and filtered through carbon, oil, and microparticle filter systems before passing through four air stock tanks into the chamber.

Air Stock Tanks

Four air stock tanks circulate filtered, dried air into the chamber to maintain the desired pressure levels consistently throughout every session.

Air Cooler

The system is connected to an air cooler to keep the air fresh inside the chamber and maintain temperature under control throughout extended multiplace sessions.

Automation System

The Automation System controls the chamber and runs sessions automatically via automation software, industrial PLC, sensors, valves, and PC. The PLC monitors and controls all connected devices, with specific functions dependent on customer configuration.

Real-Time Session Monitoring

Real-time session information is gathered from sensors and displayed to monitor session status. The monitoring systems track atmospheric pressure, oxygen concentration, temperature, humidity, patient vitals, and treatment duration, enhancing patient safety and empowering the medical team to make informed decisions.

Session Status Management

Automatic session control for speed, pressure, and time. Entry of new treatment profiles. Chamber ventilation. I/O calibration and other functions. Logging, reviewing, and printing tools. Session and patient information access. Real-time monitoring of temperature, humidity, pressure, and oxygen. Audio/visual warnings to the operator. Valve openings or maximum compression/decompression rate settings. Ear opening assistance. Session recording.

Ergonomic Seating

Tailored to the body's physiology, the ergonomic seats reduce pressure point stress and boost circulation, ensuring a relaxed and effective oxygen treatment session for each patient. Available in brandable configurations across all capacity options.

Patient Monitoring

Chamber penetrations and electrical connectors provide the capability to connect vital monitoring equipment such as EEG, ECG, TCOM, and blood pressure devices, with dedicated patient vitals monitoring screens on the control panel.

Session Data Logger

An integrated session data logger records all treatment parameters, providing a complete audit trail of every session for clinical record-keeping, quality assurance, and regulatory compliance.

Smoke Detectors

Integrated smoke detectors provide an additional layer of safety inside the pressurized environment, working in tandem with the fire suppression system to protect patients and staff.

Entertainment System

The chamber is equipped with large-screen TVs or tablets for each user, including other customizable additions to improve the in-chamber experience during long multiplace sessions.

USB Ports

USB ports are provided inside the chamber for software updates, uploading custom settings, charging devices, or downloading session archives for review and reporting.

Adjustable LED RGB Lighting

Adjustable LED RGB lighting allows operators and patients to create a personalized, serene atmosphere inside the chamber during sessions.

Ventilation

The automatic ventilation system ensures air inside the chamber is always fresh throughout the duration of every session, with a ventilation rate of 600 LPM.

Pneumatic Controls

Chamber controls are completely pneumatic in nature and require only a compressed gas source, keeping operation clean, reliable, and safe in the high-oxygen clinical environment.

Discrete Power Source

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

Customization Options

TITAN OMEGA supports extensive customization including seating capacity (4+2 up to 12+2), brandable ergonomic seat designs, brandable interior and exterior design, custom 3D epoxy flooring, different working pressure levels, and multiple entertainment and monitoring configurations.


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 is the HPOTECH TITAN OMEGA chamber engineered for?
The HPOTECH TITAN OMEGA is a 14-occupant (12+2 seat) multiplace hard-shell hyperbaric chamber featuring an omega-shaped cylindrical exterior, the largest and highest-capacity model in the HPOTECH lineup. It is engineered for high-throughput clinical operations: hospital hyperbaric departments and large HBOT centers running concurrent multi-patient sessions. The rated per-patient capacity is up to 225 kg.
What pressure does the HPOTECH TITAN OMEGA operate at?
The HPOTECH TITAN OMEGA operates across a 3.0-6.0 ATA range, up to 5.0 bar - the highest maximum pressure rating in the HPOTECH lineup and above the 3.0 ATA ceiling of the next-largest model, the Matrix. With this range, clinical teams can run higher-pressure multiplace protocols in a single chamber instead of switching equipment.
What site requirements does a TITAN OMEGA installation involve?
A HPOTECH TITAN OMEGA installation typically requires the most extensive site preparation in the multiplace lineup, scaled to its 14-occupant (12+2 seat) configuration. Most sites need reinforced floor loading, and crane rigging or specialized lifting equipment is often part of chamber ingress planning. Electrical supply capacity and the commissioning timeline are confirmed during the site-readiness review.
How do hospital departments and large HBOT centers start a TITAN OMEGA procurement?
Procurement for the HPOTECH TITAN OMEGA starts with a TITAN-specific spec brief request from the hospital or HBOT center. The engineering team reviews the facility's site plans, floor loading, access route, and electrical capacity before confirming a procurement and installation timeline scaled to the chamber's 14-occupant configuration.
What does ongoing service look like for a TITAN OMEGA operating in a high-volume clinical setting?
Post-commissioning service for the TITAN OMEGA is scaled to the high-volume clinical duty cycle of its 14-occupant configuration. Scheduled pressure-system inspections, door-mechanism servicing, and ongoing operator training support keep multiplace clinical teams current on operating procedures across the chamber's full service life.

All returns must have an RA (Return Authorization) number to be processed.
All items returned must be in new condition, in the original boxes and have the original packaging.
All accessories and chargers included in the box must be returned.
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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We will process the credit accordingly and ensure that you receive the best deal possible.

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While we are committed to providing competitive pricing, our Price Match Guarantee does come with certain limitations:

You must purchase the item from our website before requesting the Price Match Guarantee.

Promotions such as rebates, holiday sales, and "buy one, get one free" offers do not qualify.

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Our Price Match Guarantee includes both the item price and shipping charges but excludes sales tax.

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