What to do if Arjo Indoor Furnishing shows hardware failure and the repeater light is on?
If the hardware failure occurs on initial power up, it indicates an internal hardware fault, and the pump should be replaced. If it occurs during normal operation after a successful start-up, select Standby, remove the power source, re-power, and if the pump fails the BIST (Built-In Self-Test), replace the pump.
Why is there no audio alarm on my Arjo AtmosAir Velaris?
If there is no audio alarm during a fault condition and the AUDIO OFF light is lit, the audio on/off switch is likely set to the off position. If you require audio alarms and notifications to be activated, a qualified technician can set the audio on/off switch to the ON position.
General| Brand | Arjo |
|---|---|
| Model | AtmosAir Velaris |
| Category | Indoor Furnishing |
| Language | English |
Contact details for product support, maintenance, and services.
Emphasizes the importance of reading and understanding instructions for safety and operation.
Outlines routine maintenance and where to get further information or spare parts.
Procedure for reporting serious incidents involving the medical device.
Explains the meaning of warning, caution, and note indicators used in the document.
Conditions where the hybrid mattress system should not be used.
Guidelines for assessing patients, including weight limits for different system components.
Specifies the expected lifespan of the system's components (mattress, pump).
Warnings about electrical hazards, tripping, entanglement, sharp objects, heat, and CPR.
Precautions for pressure injury, mattress assembly, layers, movement device, and fire hazards.
Guidance on compatible bed frames and assessment for mattress and frame selection.
Steps to take before the first use, including package inspection and reading IFU.
Actions required before every use and after each patient.
Identifies and labels the parts of the alternating pressure pump.
Labels and identifies the buttons and lights on the control panel.
Identifies the components of the Standard and Plus mattress models.
Identifies the components of the Stretcher (ST) mattress model.
Identifies the components of the Seat Cushion.
Explains the operation of the Run/Standby and Lock buttons and their indicator lights.
Describes the function of the Audio Off light and its relation to audio notifications.
Details the buttons and lights used for setting the patient's weight on the pump.
Explains how to pause audible alarms and the associated indicator light.
Describes the Power Fail, System Fault, Low Pressure, and Skin IQ indicator lights.
Explains the normal and fault condition indications of the repeater light.
Describes the function and placement of the pump's hanging brackets.
Instructions for positioning the power cable using cable management loops.
Details the purpose and use of the Skin IQ port for connecting the coverlet.
Explains the function and location of the switch to disable pump sound notifications.
Describes the automatic brightness adjustment of pump lights in low ambient light.
Describes the mattress covers, zip, and the mattress connector.
Step-by-step guide on how to connect the pump to the mattress connector.
Step-by-step guide on how to disconnect the pump from the mattress connector.
Details the use of handles for moving the mattress and non-slip base for stability.
Instructions for securing the power cable using the loops on the mattress.
Identifies the covers, handles, and non-slip base of the ST mattress.
Identifies the covers, handle, and non-slip base of the seat cushion.
Instructions for correctly positioning the mattress on different bed or trolley frames.
Steps for hanging the pump, connecting the tube-set, and managing the power cable.
Instructions for using the mattress in reactive (unpowered) mode and patient positioning.
Steps for setting up and starting active (alternating) therapy with the pump.
Procedures for safely turning off the pump and storing it after use.
Warnings for caregivers operating the system in a home environment, covering patient injury and entanglement.
Guidelines for operating the system safely at home, including environment and supervision.
Essential safety measures during cleaning and disinfection processes.
Prohibits specific cleaning agents and methods that could damage the device.
Lists approved disinfectants and guidelines for cleaning pump and covers.
Instructions for washing and drying the removable mattress top cover.
Routine operational and visual checks performed before using the hybrid mattress system.
Procedures for cleaning, disinfecting, and inspecting components after patient use.
Explains causes and solutions for Low Pressure and Power Fail indicators.
Addresses Hardware Fail alarms and the Lock Mode feature.
Details the Audio Alarm Pause, Audio Off, and Skin IQ indicators.
Provides details on pump model, materials, size, weight, electrical ratings, and operating conditions.
Information on conditions for transport, storage, expected service life, and end-of-life disposal.
Lists compatible Skin IQ coverlets for different Arjo Velaris mattress models.
Details part numbers, sizes, materials, weights, and compatible Arjo bed frames/trolleys.
Describes features like removability, moisture permeability, antimicrobial coating, stretch, and abrasion resistance.
Information on fire retardancy, washing/drying temperatures, wipe-down chemicals, and lifetime expectancy.
Identifies and explains the product and serial number labels on the pump unit.
Identifies and explains the types of labels found on the mattress and seat cushion surfaces.
Explains common symbols like CE, MD, SN, REF, manufacturer, and manufacturing date.
Explains symbols related to electrical safety, environmental limits, and recycling.
Explains symbols for washing, drying, cleaning, facility identification, and fitting dates.
Lists the medical electrical equipment standards and certificates the product complies with.
Outlines EMC compliance, installation precautions, and warnings about interference.
Provides guidance on electromagnetic emission levels and suitability for different environments.
Details immunity test levels and recommended separation distances for RF equipment.
Explains immunity requirements for electrostatic discharge, transients, surges, and power quality variations.
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