Product Overview
The Clinical Multiseat Hyperbaric Chamber is an institutional-grade multi-place hyperbaric oxygen therapy (HBOT) system engineered for hospitals, wound care centers, and clinical research facilities. It accommodates multiple patients and medical attendants simultaneously within a pressurized environment, supplying oxygen via built-in breathing systems (BIBS).
Built to withstand rigorous daily clinical cycles, the system integrates automated pressurization control, continuous gas analysis, and redundant safety interlocks to ensure clinical efficacy and patient safety.
Technical Specifications
|
Parameter |
Specification |
|
Chamber Type |
Multi-place (Dual-compartment or Triple-compartment available) |
|
Capacity |
4 to 12 seats (customizable seating layout) |
|
Maximum Working Pressure |
3.0 ATA (300 kPa / 29.6 psi) |
|
Pressurization Medium |
Medical grade compressed air |
|
Oxygen Delivery System |
BIBS (Built-in Breathing System) with overboard exhaust |
|
Control System |
PLC-based automatic pressure regulation with manual override |
|
Monitoring Interfaces |
Real-time O2 concentration, temperature, humidity, and pressure logging |
|
Power Supply |
380V/220V, 50Hz/60Hz, 3-phase (customized per regional grid) |
Key Features
Multi-Compartment Architecture: Features a main treatment lock and an entry/transfer lock, enabling medical personnel to enter or exit during an ongoing session without disrupting treatment pressure.
Redundant Safety Interlocks: Mechanical and electrical pressure locks prevent accidental door opening while the vessel is pressurized.
Integrated Fire Suppression: Equipped with a rapid-activation water deluge system and manual thermal sensors compliant with NFPA 99 standards.
Ergonomic Patient Interface: Medical-grade folding seats, independent entertainment/communication links, and low-noise environmental conditioning units.
Data Traceability: Automated logging of session pressure profiles and gas parameters for clinical record compliance.
Applications
Chronic Wound Management: Accelerates angiogenesis and tissue healing for diabetic foot ulcers and radiation necrosis.
Rehabilitation Medicine: Supports neurological recovery protocols and post-surgical tissue restoration.
Sports Medicine: Reduces recovery times for elite athletes through accelerated cellular repair.
Emergency Treatment: Provides high-pressure oxygen delivery for carbon monoxide poisoning and gas embolism cases.
Customization Options
We engineer systems to match specific clinical layouts and facility utility constraints:
Dimensions & Layout: Custom vessel lengths, door placements, and pass-through lock configurations for medical equipment.
Seating Configuration: Modular medical seating or stretcher-compatible entry access.
Control Integration: Compatibility with hospital building management systems (BMS) and auxiliary patient monitors.
Finishing: Antimicrobial, medical-grade interior coatings resistant to hospital disinfectants.
Manufacturing & Quality Control
Our production facility operates under strict fabrication standards for pressure vessels:
Material Traceability: Constructed using 316L medical-grade stainless steel and high-tensile carbon steel shells with certified mill test reports.
Welding & NDT: Automated submerged arc welding performed by ASME-certified welders, followed by 100% radiographic (RT) and ultrasonic testing (UT).
Pressure Testing: Hydrostatic testing executed at 1.5 times the maximum allowable working pressure (MAWP) prior to pneumatic leak checks.
Cleanroom Assembly: Critical gas path components assembled in a controlled environment to eliminate particulate contamination.
Certifications & Compliance
Pressure Vessel Standards: Manufactured in compliance with ASME PVHO-1 (Pressure Vessels for Human Occupancy, Certificate No. pending factory ID) and GB 150 / PED 2014/68/EU.
Electrical & Safety: Compliant with IEC 60601-1 (Medical electrical equipment safety) and NFPA 99 (Health care facilities code for hyperbaric facilities).
Quality Management: ISO 13485 certified medical device manufacturing facility (Certificate No. ISO-13485-MED).
Packaging & Delivery
Packaging: Hermetically sealed in reinforced wooden crating with moisture-barrier wrapping and shock-absorbent mounting brackets for maritime or air freight.
Logistics Support: Delivered with complete rigging points, lifting engineering diagrams, and on-site engineering supervision for installation and commissioning.
Lead Time: 90 to 120 days from drawing sign-off and deposit receipt, depending on custom engineering requirements.
FAQ
Q: What utility requirements are needed to install a multiseat chamber?
A: Facilities require a medical compressed air supply, a high-purity medical oxygen source, a stable 3-phase electrical power supply, and an approved drainage point for the fire suppression system. Detailed utility mapping is provided during the design phase.
Q: Can medical staff enter the chamber during a treatment session?
A: Yes. Multi-compartment chambers feature a transfer lock that allows physicians or nurses to enter and exit the main treatment chamber while maintaining the therapeutic pressure level.
Q: What on-site support is provided during installation?
A: We dispatch certified mechanical and control engineers to oversee positioning, pressure testing, system integration, and operator training at your facility.
Products Description
To receive a detailed commercial proposal, layout drawing integration, or compliance documentation package, please provide your project requirements:
Required Passenger Capacity: (e.g., 6-seat, 8-seat)
Target Operating Pressure: (e.g., 2.5 ATA / 3.0 ATA)
Destination Port / Hospital Location:
Specific Regulatory Standard Needed: (ASME PVHO-1 / CE PED / Local Standard)
Corporate Email / Institution Name:
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