Modular Hyperbaric Treatment Chamber
The Modular Hyperbaric Treatment Chamber is engineered for clinical hyperbaric oxygen therapy (HBOT), providing scalable multi-place configurations to fit hospital spatial constraints and patient throughput requirements. Built with modular lock designs, the system allows flexible expansion from single-lock monoplace setups to multi-compartment systems supporting simultaneous treatments for multiple patients and medical attendants.
Technical Specifications
|
Parameter |
Specification |
|
Chamber Type |
Multi-place, modular configuration (Main Lock + Entry Lock) |
|
Maximum Working Pressure |
Up to 3.0 ATA (300 kPa / 43.5 psi) |
|
Occupancy Capacity |
Configurable from 2 to 12+ patients (plus attendant seats) |
|
Pressure Vessel Standard |
ASME PVHO-2, Pressure Equipment Directive (PED), IEC/UL compliant electrical sub-systems |
|
Oxygen Delivery System |
Built-in Breathing System (BIBS) with overboard dump |
|
Fire Suppression |
Automated and manual water-mist deluge system per NFPA 99 |
|
Environmental Control |
Integrated HVAC for temperature and humidity regulation |
|
Viewports |
Acrylic viewports manufactured to ASME PVHO requirements |
Key Features
Modular Multi-Lock Architecture: Separate entry and treatment locks permit pressurization and depressurization cycles without interrupting ongoing therapies.
Medical-Grade Life Support: Continuous gas monitoring, automated pressure regulation, and failsafe mechanical relief valves.
Ergonomic Interior Layout: Flame-retardant medical seating, customizable stretcher mounts, and low-noise environmental conditioning.
Advanced BIBS Integration: Low-resistance demand regulators supply 100% medical oxygen directly to patients while exhausting exhaled gas outside the pressure envelope.
Digital Control Console: PLC-based master control panel featuring automated pressure profile execution, real-time gas analysis, and manual override capabilities.
Applications
Chronic Wound Management: Treatment of diabetic foot ulcers, radiation necrosis, and non-healing grafts.
Emergency Intervention: Rapid decompression sickness (DCS) and arterial gas embolism management.
Rehabilitation & Neurology: Adjunctive care protocols for ischemic conditions and post-surgical recovery.
Customization Options
Spatial Layout: Right-angle or linear lock placement configurations tailored to hospital room dimensions.
Medical Interfaces: Custom pass-through penetrators for infusion pumps, ECG monitors, and ventilator tubing.
Seating Configurations: Interchangeable treatment chairs and foldable medical stretcher accommodation.
Manufacturing & Quality Control
Material Traceability: Fabricated from SA-516 Grade 70 pressure vessel steel with 100% full-penetration radiographic weld inspection.
Machining & Welding: Automated submerged arc welding (SAW) and TIG welding performed by certified ASME Section IX welders.
In-House Testing: Hydrostatic pressure testing executed at 1.5x maximum allowable working pressure (MAWP) prior to pneumatic leak checks.
Surface Treatment: Internal medical-grade anti-microbial coating applied in a controlled cleanroom environment.
Certifications & Compliance
ASME PVHO: Pressure Vessel for Human Occupancy certified.
ISO 13485: Medical devices quality management systems certification.
CE Compliance: Conforms to EU Medical Device Regulation (MDR) and Pressure Equipment Directive (PED).
NFPA 99: Compliant with health care facilities code standards for hyperbaric facilities.
Packaging & Delivery
Transport Protection: Shock-mounted vacuum-sealed barrier packaging with moisture-absorbing desiccants.
Logistics Support: Containerized sea freight or specialized heavy-lift air charter coordination with on-site rigging supervision available.
Documentation: Complete Dossier including Material Test Reports (MTRs), weld maps, NDT reports, and factory acceptance test (FAT) certificates supplied upon delivery.
FAQ
Q: What utility connections are required on-site?
A: The system requires dedicated medical gas supplies (Oxygen, Medical Air, Instrument Air), a continuous electrical power feed with backup generator integration, and a chilled water or HVAC tie-in for environmental control.
Q: What is the standard manufacturing lead time?
A: Production runs between 16 to 24 weeks, depending on modular complexity, third-party inspection schedules, and custom integration requirements.
Q: How is routine maintenance handled?
A: Annual inspection protocols cover viewport thickness verification, pneumatic valve seal replacements, and calibration of gas analyzers, supported by comprehensive technical documentation supplied with the unit.
Request a Quote
To receive a detailed technical proposal, layout drawings, and project quotation tailored to your clinical facility specifications, submit your requirements to our engineering team:
Required Project Details: Anticipated patient throughput, available room dimensions, target pressure rating, and required third-party inspection agency (e.g., Lloyd's Register, TÜV, SGS).
Direct Inquiry: [Insert Corporate Email / RFQ Submission Link]
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