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10 LPM High-Flow Stationary Oxygen Concentrator
The 10 LPM High-Flow Stationary Oxygen Concentrator is built for institutional and commercial environments requiring a stable, high-volume on-site oxygen supply. Optimized for extended 24/7 duty cycles, this platform maintains rigorous purity levels under continuous operational stress.
Features
The 10 LPM High-Flow Stationary Oxygen Concentrator is built for institutional and commercial environments requiring a stable, high-volume on-site oxygen supply. Optimized for extended 24/7 duty cycles, this platform maintains rigorous purity levels under continuous operational stress.
Our core architecture utilizes advanced Pressure Swing Adsorption (PSA) principles to deliver reliable, oil-free medical-grade gas streams without the logistical complexities of high-pressure cylinders.
Technical Specifications
|
Parameter |
Specification Details |
|
Product Type |
Stationary Oxygen Concentrator |
|
Maximum Flow Rate |
10 LPM |
|
Oxygen Concentration |
93% (plus-minus 3%) at rated 10 LPM flow |
|
Technology |
Pressure Swing Adsorption (PSA) |
|
Power Supply |
AC 220V/110V, 50/60Hz [Configurable per destination] |
|
Noise Level |
Less than or equal to 50 dB(A) |
|
Operating Duty Cycle |
Rated for 24/7 continuous operation |
|
Alarm Architecture |
Power failure, high/low pressure, low purity, thermal overload |
|
Dimensions & Net Weight |
[Insert L x W x H dimensions and Net Weight] |
|
Quality Management |
ISO 13485 Certified Production Facility |
Critical Evaluation Factors for Technical Selection
1. Purity Stability at Maximum Output
Verify that nominal 10 LPM ratings do not compromise oxygen concentration. Our engineering test curves confirm stable purity performance (typically 93% plus-minus 3%) across the entire operating flow range.
2. Outlet Pressure & Backpressure Limits
Ensure delivery pressure matches downstream delivery requirements or local pipeline specifications. Confirm allowable backpressure thresholds to prevent flow choking.
3. Thermal Management & Duty Cycle
Equipped with oversized compressor displacement and optimized internal airflow channels to suppress thermal accumulation during uninterrupted, round-the-clock operation.
Manufacturing, Materials, and Quality Control
As an integrated medical device manufacturer, our factory processes ensure absolute lot traceability and structural reliability:
Molecular Sieve Bed: Packed with high-efficiency zeolite material engineered for optimized nitrogen-oxygen separation and longevity.
Pneumatic Valve Integrity: Precision solenoid switching manifolds tested for multi-million cycle endurance to guarantee consistent pressure swings.
Rigorous Burn-In Protocols: Every completed unit undergoes automated gas chromatography analysis and a mandatory multi-hour continuous burn-in run prior to packaging.
Compliance Standards: Manufactured under strict ISO 13485 quality management guidelines.
Target Application Environments
This high-flow platform supports a variety of institutional use-cases, subject to local regulatory clearance and proper system design:
Healthcare Institutions: Supporting fixed institutional oxygen support requirements.
Specialized Care Facilities: Nursing homes and clinics requiring steady high-volume output.
System Integration: Engineering projects requiring modular on-site gas generation.
Customization & Partnership Support
We empower international medical brands and regional partners through comprehensive tailoring capabilities:
Private Labeling: Custom casing colors, brand logos, and localized multilingual user manuals.
Electrical Adaptation: Voltage and plug configurations customized for target markets (North America, Europe, UK, etc.).
Export Packaging: Drop-tested, reinforced corrugated master cartons designed for global maritime and air freight.
Frequently Asked Questions
Q: Does the unit sustain 93% purity at full 10 LPM delivery?
A: Yes. Our internal PSA configuration is balanced to maintain nominal oxygen concentration (93% plus-minus 3%) at maximum rated continuous flow. Performance verification curves are available upon request.
Q: What are the primary scheduled maintenance tasks?
A: Routine upkeep involves washing or replacing external cabinet filters periodically, replacing intake particle filters annually, and observing recommended service schedules detailed in the manual.
Q: What documentation is provided for regulatory review?
A: We supply factory inspection records, ISO 13485 certificates, complete user manuals, and technical datasheets. Specific local market registration documents can be coordinated through our export team.
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