Clinical HBOT Chamber | B2B Product Specification & Procurement Page
The Clinical HBOT Chamber is a heavy-duty, medical-grade hyperbaric oxygen system engineered for hospitals, wound care centers, and specialized rehabilitation clinics. Built for continuous clinical operation, it delivers therapeutic pressures ranging from 1.5 ATA to 3.0 ATA combined with a medical-grade Built-In Breathing System (BIBS).
Designed to integrate directly into clinical infrastructure, this system meets stringent international medical device regulations, ensuring patient safety, precise pressure control, and reliable long-term performance under demanding hospital schedules.
Technical Specifications
|
Parameter |
Specification |
|
Operating Pressure |
1.5 ATA to 3.0 ATA (Adjustable in 0.1 ATA increments) |
|
Chamber Type |
Hard-shell steel/aluminum alloy (Monoplace / Multi-place configurations available) |
|
Oxygen Supply |
100% O2 via medical BIBS masks; ambient chamber gas is filtered medical air |
|
Pressurization Medium |
Medical grade compressed air (Oil-free scroll/screw compressors) |
|
Control System |
Automated PLC touchscreen interface with manual override backups |
|
Safety Features |
Automatic pressure relief valves, emergency depressurization (< 60 seconds), built-in NFPA 99 compliant water mist fire suppression system |
|
Internal Environment |
Integrated climate control (Temperature & Humidity regulation), LED medical lighting, intercom system |
|
Power Requirements |
380V/220V, 50Hz/60Hz, 3-phase (customizable per regional grid) |
Key Features
Redundant Safety Architecture: Dual-redundant mechanical and electronic pressure regulators prevent over-pressurization. Emergency manual exhaust valves remain operational during total power loss.
Medical-Grade BIBS: Closed-loop or exhaled-gas scavenging BIBS ensures patients breathe pure oxygen while preventing oxygen enrichment inside the main chamber hull.
Precision PLC Automation: Automated compression, treatment, and decompression profiles minimize operator error while allowing custom clinical protocols.
Ergonomic Patient Interface: Acrylic viewing ports (acryl-glass) eliminate claustrophobia, paired with medical-grade patient seating/stretchers rated for high weight capacities.
Integrated Diagnostics: Real-time monitoring sensors track internal oxygen concentration, carbon dioxide levels (CO2 scrubbed continuously), temperature, and humidity.
Applications
Wound Care & Hyperbaric Centers: Accelerated healing for chronic diabetic foot ulcers, radiation tissue damage, and compromised skin grafts.
Emergency Medicine: Treatment protocols for acute carbon monoxide poisoning, gas embolism, and severe decompression sickness.
Neurological & Orthopedic Rehabilitation: Adjunctive therapy for post-stroke recovery, traumatic brain injury (TBI) rehabilitation, and sports medicine tissue repair.
Customization Options
Capacity Configuration: Available as single-patient monoplace units or multi-place chambers accommodating 2 to 12 patients plus a medical attendant.
Layout & Port Placement: Custom positioning for gas inlet/outlet ports, electrical pass-throughs for patient monitors, and IV line entry ports.
Exterior Finish: Medical-grade powder-coated steel finish in hospital-specified color palettes, or brushed stainless steel shrouds.
OEM/ODM Services: Private labeling, custom software UI branding, and localized electrical compliance integration.
Manufacturing & Quality Control
Weld Integrity: All pressure hulls utilize automated TIG/MIG welding performed by ASME-certified welders, followed by 100% X-ray and ultrasonic non-destructive testing (NDT) on structural seams.
Material Traceability: Hulls are fabricated from certified marine-grade stainless steel or high-tensile aluminum alloys with complete mill test certificates.
Pressure Testing: Every chamber undergoes hydrostatic testing at 1.5x maximum allowable working pressure (MAWP) prior to pneumatic functional testing.
Cleanroom Assembly: Oxygen-contact components are cleaned, degreased, and assembled in ISO Class 7 cleanrooms to eliminate hydrocarbon contamination risks.
Certifications & Compliance
Regulatory Status: Manufactured under ISO 13485 medical device quality management standards.
Safety Codes: Complies with ASME PVHO-1 (Pressure Vessels for Human Occupancy), NFPA 99 (Health Care Facilities Code - Hypobaric/Hyperbaric Facilities), and CE Directive 93/42/EEC (MDR equivalent).
Packaging & Delivery
Transport Protection: Shipped in sealed, fumigation-free wooden crates with shock-absorbent mounting and moisture-barrier vacuum sealing for electronics and acrylic components.
Logistics Support: Delivered via specialized flatrack container or heavy-lift air freight, complete with crating schematics and rigging anchor points.
Installation Support: Engineering documentation (P&ID diagrams, site preparation manuals) provided pre-shipment; optional on-site commissioning and operator training by certified factory technicians.
FAQ
Q: What site preparation is required prior to installation?
A: Facilities require a reinforced concrete floor capable of supporting the chamber weight (>= 1.5 to 4 tons depending on model), medical-grade compressed air supply lines, a pure oxygen source (liquid O2 tank or high-pressure cylinder manifold), and proper room ventilation/HVAC integration per NFPA 99.
Q: What is the standard lead time for manufacturing?
A: Standard monoplace chambers require 45 to 60 days. Multi-place or highly customized systems require 90 to 120 days, inclusive of NDT testing and regulatory documentation preparation.
Q: How is routine maintenance handled?
A: Routine maintenance involves replacing CO2 absorbent granules, inspecting BIBS valves, calibrating oxygen sensors every 6 months, and annual safety valve recertification. We supply comprehensive spare parts kits with each unit.
Request A Quote
To receive an itemized quotation including freight estimates, utility layout requirements, and regulatory documentation packages tailored to your facility, please specify your project parameters below:
Required Chamber Type (Monoplace / Multi-place / Capacity)
Delivery Destination (Port / Hospital Location)
Target Regulatory Standard (CE / ASME / Local Code)
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