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Medical Oxygen Concentrator With Alarm System
Utilizing Pressure Swing Adsorption (PSA) technology, the system separates oxygen from ambient nitrogen to deliver a continuous, medical-grade oxygen stream. The integrated monitoring suite is engineered to track critical operating variables continuously, minimizing operational risks associated with electrical fluctuations, compressor stress, and molecular sieve wear.
Features
Utilizing Pressure Swing Adsorption (PSA) technology, the system separates oxygen from ambient nitrogen to deliver a continuous, medical-grade oxygen stream. The integrated monitoring suite is engineered to track critical operating variables continuously, minimizing operational risks associated with electrical fluctuations, compressor stress, and molecular sieve wear.
Every unit undergoes multi-point factory testing covering flow rate accuracy, acoustic output suppression, electrical safety isolation, and gas purity stabilization before final assembly sign-off.
Technical Specifications & Engineering Standards
|
Technical Parameter |
Specification Standard (Model Dependent) |
|
Generation Technology |
Pressure Swing Adsorption (PSA) |
|
Rated Flow Output |
0 to 5 L/min or 0 to 10 L/min configurations |
|
Oxygen Concentration |
93% (plus or minus 3%) at rated operational flow |
|
Outlet Pressure |
0.04 to 0.07 MPa (adjustable output options available) |
|
Standard Alarm Array |
Power failure, low purity, high/low pressure, thermal overload |
|
Acoustic Noise Level |
Less than or equal to 50 dB(A) (measured at 1 meter distance) |
|
Electrical Power Input |
AC 220V plus or minus 10%, 50/60 Hz or AC 110V, 60 Hz |
|
Power Consumption |
Less than or equal to 350W to 600W (tier-dependent) |
|
Operational Duty Cycle |
Engineered for 24/7 continuous operation under recommended maintenance |
|
Environmental Limits |
Temperature: 10°C to 40°C; Relative Humidity: less than or equal to 80% |
Integrated Alarm System & Monitoring Logic
Alarm coverage dictates equipment reliability in professional settings. The built-in electronic monitoring suite triggers distinct auditory and visual notifications under specific operational exceptions:
Power Failure Warning: Activates immediately upon total loss of external AC power or accidental disconnection of the supply cord.
Low Purity Alert: Triggers if internal sensors detect oxygen concentration falling below established safety baselines (typically adjustable to less than 82% to 85%).
Pressure Anomaly Notification: Identifies operating pressures operating outside designated safe thresholds, safeguarding internal compressor components and molecular sieve beds.
Flow Obstruction Warning: Detects downstream flow restrictions, pinched delivery tubing, or internal pathway blockages.
Thermal Protection Alert: Warns operators when internal cabinet or compressor temperatures exceed safe operating limits.
Application Suitability & Operating Boundaries
Outpatient Clinics & Care Facilities: Suitable for localized oxygen therapy where a self-contained, mobile oxygen source with safety monitoring is specified.
Equipment Distribution Networks: Built for regional distributors requiring stable batch consistency, customized labeling, and complete technical manuals.
Institutional Healthcare Projects: Applicable for standard ward setups aligning with local facility guidelines.
Quality Control & Manufacturing Verification
To support stringent technical audits and regulatory compliance verification, the manufacturing process maintains strict internal controls:
Component Screening: 100% incoming inspection for oil-free compressors, molecular sieve purity grades, and electronic sensor circuit boards.
Burn-in Testing: Finished units undergo extended operational aging cycles to verify thermal stability, continuous pressure output, and sensor calibration accuracy.
Traceability Records: Every unit is assigned a unique serial number linked to production testing logs covering electrical safety and gas purity verification.
Packaging, Shipping & Logistics Verification
Professional distribution requires rigorous transport protection and logistics planning. Equipment packaging and delivery standards include:
Shock-Absorbing Protection: Units are secured within high-density molded foam inserts and reinforced multi-layer export cartons (or fumigation-free wooden crates for bulk pallet shipments) to prevent transport shock damage.
Accessory Kit Inclusion: Each package includes standard intake air filters, humidifier bottles, nasal cannula kits, power cords, and model-specific user manuals.
Logistics Stability: Export packaging complies with international transit moisture and drop-test standards, ensuring safe arrival across ocean and air freight channels.
FAQ
Q: Can alarm thresholds be adjusted for specific tender or institutional requirements?
A: Standard alarm thresholds are pre-calibrated to comply with international medical device norms. For large-scale customization projects, specific alarm logic or display language options can be evaluated during the technical agreement phase.
Q: What documentation is provided for customs clearance and product registration?
A: Standard shipments include manufacturing batch reports, Certificates of Analysis (CoA), factory inspection records, user manuals, and technical datasheets. Specific regulatory filings required for destination markets should be confirmed with the export support team prior to order placement.
Q: What is the recommended maintenance schedule for internal alarm sensors?
A: External intake air filters should be cleaned weekly and replaced every 3 to 6 months depending on environmental dust levels. Oxygen purity sensors and internal electronic components are designed for long-term stability but should be functionally tested during annual routine maintenance.
Q: What technical details are required to initiate a wholesale quotation?
A: Please provide the required flow rate tier, estimated order volume, destination country, electrical plug standard, and any private labeling or custom documentation needs.
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