Multiplace hyperbaric chamber

SAMA MP-Series

Multiplace hyperbaric chamber for hospital units that need to treat multiple patients in a single session.

SAMA MP-Series — multiplace hyperbaric chamber by OHB Industries

Overview

In-depth notes on engineering choices, intended use, and how the SAMA MP-Series integrates into your facility.

The SAMA MP-Series is OHB's multiplace hyperbaric chamber, designed for hospital units and reference centers that need to treat multiple patients in a single session, with life-support compatibility and an interior configured to the clinical workflow of the institution.

When a multiplace is justified

The decision to implement a multiplace unit typically responds to sustained patient volume, the need to treat critical cases with a clinical attendant inside the chamber, or programs combining hyperbaric oxygen therapy with critical care. The MP-Series is the appropriate platform for general hospitals, oncology centers with wound-care programs, and regional reference centers.

Built-to-spec dimensions

MP-Series dimensions (external height, length, and width) are defined per project to maximize the available suite footprint. As a reference, the minimum external length is 1000 mm and minimum external width is 600 mm — however, each unit is sized to the number of seats, life-support equipment, and clinical workflow. Maximum working pressure is 100 PSI (~7.8 ATA absolute), with compressed-air supply up to 140 PSI and O₂ up to 70 PSI.

Life support and interior configuration

The interior is configured for seated or reclined patients with a clinical attendant accessible throughout the session. The system integrates a personnel airlock, attendant air-break supply, and compatibility with ventilators, IV pumps, and monitors capable of operating in the pressurized environment. This enables treatment of higher-complexity patients while preserving continuity of care.

Hospital-grade compliance

The MP-Series is engineered with reference to internationally recognized pressure-vessel, safety, medical-equipment, healthcare-facility and multiplace-chamber design criteria, making it suitable for hospital installations while reviewing the applicable regulatory pathway per destination market. Each project includes a technical feasibility study, suite design, installation engineering, functional testing, and technical documentation available upon request.

Service and operational continuity

An annual maintenance contract is recommended for multiplace units, with preventive visits, prioritized spare parts, and technical phone support. This coverage reduces the risk of unplanned downtime and preserves the unit's operational authorization.

Technical highlights

  • Multi-patient seating with attendant access
  • Built-in attendant air-break system
  • Hospital-grade life-support compatibility
  • Configurable interior for clinical workflow

Typical applications

  • Hospital hyperbaric units
  • Reference HBOT centers
  • Critical-care-capable facilities
  • Research and academic centers

Technical specifications

Standard configuration. Values can be tuned to clinical protocol, facility infrastructure, and local regulations. Full datasheet with drawings available on request.

Type
Multiplace hospital chamber
Maximum working pressure
100 PSI (~7.8 ATA absolute)
Maximum compressed-air supply pressure
140 PSI
Maximum O₂ supply pressure
70 PSI
Dimensions
Built to spec — external height, length and width are defined per project to fit the hyperbaric unit, clinic or hospital footprint
Minimum external length (reference)
1000 mm
Minimum external width (reference)
600 mm
Design references
Internationally recognized pressure-vessel, safety, medical-equipment, healthcare-facility and multiplace-chamber criteria — documentation available upon request; regulatory pathway reviewed per destination market
Life support
Compatible with ventilators, IV pumps, monitors
Warranty
24 months + annual maintenance contract

Design references: OHB chambers are engineered with reference to internationally recognized pressure-vessel, safety and medical-equipment design criteria. Applicable compliance documentation is reviewed according to configuration, intended use and destination market, and is shared under NDA during the evaluation process. Clinical use must be indicated and supervised by qualified medical professionals.

FAQ

SAMA MP-Series — common questions

The configuration is defined per project based on expected volume, life-support requirements, and clinical workflow. Dimensions are sized to your available suite footprint.

Request SAMA MP-Series specifications

Send your facility profile and intended use — we'll return full technical documentation, configuration guidance, and pricing context.

Prefer email? Write to ohb@grupohiperbarica.com.