What to do if Arjo Flowtron ACS900 shows 'Battery Low'?
If your Arjo Medical Equipment displays a 'Battery Low' message, connect the pump to the mains power supply. This will recharge the battery, allowing you to continue therapy.
What to do if Arjo Medical Equipment indicates 'High Temperature'?
If your Arjo Medical Equipment indicates a 'High Temperature', ensure the pump isn't near a heat source or covered by blankets. If the internal temperature exceeds 60°C, switch off the pump and allow it to cool down.
What to do if Arjo Flowtron ACS900 Medical Equipment displays 'Low Pressure/Leak'?
If your Arjo Medical Equipment is showing a 'Low Pressure/Leak' warning, examine the garment and tubing for any leaks. Repairing the leak should clear the warning. If the alarm persists after repair, replace the affected garment.
What to do if the Arjo Medical Equipment garment is disconnected?
If the garment of your Arjo Medical Equipment becomes disconnected, reconnect or replace it. Reconnecting the garment should clear the warning or alarm.
What to do if Arjo Flowtron ACS900 Medical Equipment tube is kinked or blocked?
If you suspect a kinked or blocked tube in your Arjo Medical Equipment, examine the garment and tubing for any obstructions. Removing the kink or blockage should clear the warning. If the alarm continues, consider replacing the affected garment.
General| Type | Sequential Compression Device |
|---|---|
| Model | ACS900 |
| Pressure Settings | Adjustable |
| Intended Use | Deep Vein Thrombosis (DVT) prophylaxis |
| Compression Mode | Sequential |
| Power Supply | 100-240V AC, 50/60 Hz |
| Alarms | Cuff Disconnect, Low Pressure |
| Cuff Options | Thigh, Foot |
| Safety Features | Overpressure protection, automatic shut-off |
| Application | Used in hospitals and clinics for patients at risk of DVT |
| Dimensions | 30 x 25 x 15 cm |
Caregiver responsibility, cable positioning, avoiding hazards, and proper usage guidelines.
Safety measures against fire, sunlight, and use of approved cleaning solutions.
EMC compliance, expected service life, end of life disposal, and environmental protection.
Guide to manual use, system description, and its function in augmenting blood flow.
Helps prevent Deep Vein Thrombosis (DVT) in hospitals and healthcare facilities under supervision.
Outlines the intended use for DVT prevention and lists conditions where use is contraindicated.
Essential for proper garment application, positioning to avoid pressure points, and skin inspection.
Initiate therapy promptly, ensure proper garment fit, instruct patients, and apply pre/post-operatively.
Describes the main control panel, LCD screen, and power button functions for operation.
Details functions of control buttons and explains various icons displayed on the LCD screen.
Explains garment type display, connector identification, therapy control, and pressure settings.
Details mains power, battery status, system initialisation, and patient run time displays.
Explains audible alarm status, muted alarms, warning/alarm icons, and LED indicators on the pump case.
Covers routine operation, pump installation, and the startup process with diagnostic tests.
Shows standby screens based on garment connection and how to connect garments.
How to initiate therapy, recommended checks, and example of two foot garments.
Procedures for stopping therapy, putting the pump in standby, and switching the pump off.
How the pump indicates faults and how to adjust audible alarm volume settings.
How to reset patient run hours and information on therapy settings adjustment.
Recommended procedures for cleaning and chemical disinfection of the system components.
Details maintenance-free design, servicing recommendations, general care, and serial label information.
Explains fault detection, warning/alarm conditions, and refers to a troubleshooting table and service manual.
Details warnings/alarms for Low Pressure/Leak, Kinked/Blocked Tube, Garment Disconnected, Service Required.
Details warnings/alarms for Battery Low, including conditions and corrective actions.
Details warnings/alarms for Faulty Tubeset and High Temperature conditions.
Details warnings/alarms for Hardware Fail and Tubeset Disconnected/Calibration Required.
Lists compatible calf, calf & thigh, and foot garments with their types, sizes, and therapy modes.
Details pump model, power input, size, weight, material, fuse rating, and protection degrees.
Specifies operating and storage conditions regarding temperature, humidity, and atmospheric pressure.
Declares compliance with RF emissions standards and provides guidance on electromagnetic environment.
Recommends minimum separation distances for RF communications equipment based on transmitter power.
Declares immunity compliance with IEC 60601 standards and provides guidance on electromagnetic environment.
Explains various symbols used on the product and in the manual for safety and operational understanding.
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