Founded in 1997, Chengdu Lianbang Medical Technology Co., Ltd. has deeply engaged in the fields of medical gas systems and hyperbaric oxygen technology, gradually developing into a leading enterprise in the industry. Its series of clinical hyperbaric chamber products integrate decades of scientific research achievements, clinical practice experience and industry collaboration wisdom, building a differentiated competitive advantage and setting a new benchmark in the industry.
Comprehensive Safety Assurance System
Multi-layer pressure monitoring system combined with redundant safety design to eliminate over pressure risks from the source and ensure stable operation of the chamber;
Adopting fire prevention and explosion suppression technology that meets international medical safety standards to fully avoid potential safety hazards during treatment;
Preset emergency decompression procedures to enable rapid patient evacuation in emergency situations and improve emergency response capabilities;
Supports integration of real-time vital sign monitoring systems to track patients' physical conditions throughout the treatment and respond to abnormalities in a timely manner.
Diversified Clinical Adaptability
|
Chamber Type |
Key Applications |
Ideal Settings |
|
Monoplace Chambers |
Intensive care, wound management, neurological rehabilitation treatment |
General hospitals, specialty clinics |
|
Multiplace Chambers |
Group therapy, pediatric diagnosis and treatment, complex cases requiring full-time medical attendance |
Large medical centers, university-affiliated hospitals |
|
Portable Clinical Units |
Emergency rescue, medical services in remote areas |
Field hospitals, mobile medical institutions |
Lianbang Clinical Hyperbaric Chambers strictly comply with global medical device regulatory requirements and have passed a number of international authoritative certifications to ensure product quality and clinical safety, gaining wide recognition from healthcare professionals around the world:
ISO 13485 Medical Device Quality Management System Certification;
CE Certification, complying with European medical market access standards;
Local medical device registration certifications covering Asia, the Middle East, Latin America and other regions.
Each chamber undergoes rigorous pressure cycle testing, material stress analysis and safety protocol verification before being put into use to ensure stable operation in high-load clinical environments.