Summary of Contents for Care of Sweden CuroCell iA Automatic
Page 1
Instructions for use 2023-05-16 CuroCell® iA Automatic & CuroCell® iA Manual Air mattress systems Instructions for use item number: 95-001456-EN0000...
5.7 Hand check (function control) ..... 15 Table of contents 5.8 CPR (Cardiopulmonary resuscitation) .. 15 1 Introduction ........3 5.9 Restart ..........15 1.1 General information ......3 5.10 Power failure ........15 1.2 Intended purpose ........3 5.11 Notifications ........15 1.3 Intended user ........
Page 3
The product must only be installed and used for its intended purpose according to the instructions in this manual and/or other documentation from Care of Sweden. The product must not be combined, assembled or repaired with parts (e.g. control unit and mattress), accessories or spare parts other than those described in this manual or other documentation from Care of Sweden.
Page 4
Contact an authorized service technician for examination and repair. Never connect anything other than the Care of Sweden supplied power supply to the control unit power cable connector.
Care of Sweden. and decide whether the characteristics of the Intended purpose mattress is beneficial for the patient based on The mattress system consists of a control unit diagnosis.
12 hours. Assembly and installation Check that no parts are damaged. If damage is found, contact Care of Sweden or your local distributor before using the product. Do not use sharp objects when unpacking as it might damage the product.
Page 7
4. Open the lid on the air tube connector 7. Check that the power cable has been (marked CPR) and connect it to the side of the correctly connected to the control unit and that control unit. the correct power supply has been used. (See section 11 Technical specification).
Common operations Following operations apply to CuroCell® iA Automatic and CuroCell® iA Manual regardless of which mattress that is used. 3.1 CPR (Cardiopulmonary resuscitation) In case of an emergency where CPR (Cardiopulmonary resuscitation) is necessary, remove the connection (marked ‘CPR’) from the control unit and leave the lid open to empty the mattress of air quickly.
CuroCell® iA Automatic Operation CuroCell® iA Automatic Following operations apply only to CuroCell® iA Automatic regardless of which mattress that is used. Read the label of the control unit carefully to make sure that you know which control unit you have. Operation CuroCell®...
Page 10
® CuroCell iA Automatic Button Function Mute the information signal Panel lock Gentle Alternating Low Pressure (GALP) Constant Low Pressure (CLP) Maximum pressure (caring mode) Information signal Incorrect connection of the air connector (CPR) Cycle time settings (10, 15, 20, 25 minutes). The diodes are also used for error notifications.
® CuroCell iA Automatic Maximum pressure (caring mode) Automatic setting With this function, the entire mattress The mattress system independently and is inflated and provides firmed without manual adjustment controls the inner support. This function reverts to the pressure of the mattress according to the previous setting after 20 minutes.
® CuroCell iA Automatic Hand check (function control) CPR (Cardiopulmonary resuscitation) Hand check is performed to ensure that the See 3.1 mattress system works properly. Hand check Restart should be performed regularly; for CuroCell® iA See 3.2 Automatic we recommend once every eight Power failure hours as well as after installation of the system.
Page 13
CuroCell® iA Automatic Notification (audible and visual) Description and troubleshooting High temperature. Valves and compressors are turned off. If the control unit is in direct sunlight, relocate it. If problem persists, contact an authorized service technician. Default settings are not completed. Contact an authorized service technician.
CuroCell® iA Manual Operation CuroCell® iA Manual Following operations apply only to CuroCell® iA Manual regardless of which mattress that is used. Read the label of the control unit carefully to make sure that you know which control unit you have.
Page 15
CuroCell® iA Manual Button Function Mute the information signal Panel lock Gentle Alternating Low Pressure (GALP) Constant Low Pressure (CLP) Maximum pressure (caring mode) Patient weight settings Information signal Incorrect connection of the air connector (CPR) Seating function Cycle time settings (10, 15, 20, 25 minutes). The diodes are also used for error notifications.
CuroCell® iA Manual Seating function Manual setting A visible and audible notification is At start-up, the inner pressure of the mattress generated when the seating function must be set manually based on the weight and has been active for two consecutive height of the patient.
CuroCell® iA Manual Hand check (function control) 3. If you can feel the patient’s sacrum resting in Hand check is performed to ensure that the the palm of your hand, the gap is too small. See mattress system works properly and to ensure section 10 ‘Troubleshooting’.
CuroCell® iA Manual 5.13 Table of notifications Information about each notification is shown in the notification table: • Some of the notifications are both audible and visual. The error code will be displayed until the error has been rectified. If the mute button is pressed the audible warning will crease for a period of 5 minutes and will return until the error has been rectified.
CuroCell® iA Manual Product description Make sure that you read about the right product by looking at the label of the control unit as well as the mattress. Product combinations Below is a table showing which products that are possible to combine with each other. Control unit Mattress Mattress cover...
Page 20
Control panel Tube/CPR connection Power switch, On/Off Connection power cable Air filter Hangers Power supply CuroCell ® iA Manual CuroCell ® iA Automatic...
Disinfection is recommended between patients according to the instructions below. Always follow local instructions and the instructions for use of the cleaning and disinfecting agent. Consult your hygiene manager or Care of Sweden for help and instructions in case of uncertainty. Cleaning and disinfection CONTROL UNIT Wipe the control unit with a damp cloth and mild detergent.
Disinfection of mattress 1. Disinfect all external surfaces of the mattress with disinfectant according to section 7.1 Cleaning and disinfection - Inner cover and Mattress cover - Wipe off. Ensure that all areas are free of dirt residue. 2. Allow the disinfectant to work according to the instructions from the manufacturer of the agent. 3.
Service and maintenance The control unit should be regularly serviced and inspected to maintain functionality and performance. Only use spare parts approved by Care of Sweden. Service and maintenance chart Service in the column to the right must only be performed by an authorized service technician.
If the control unit is used in a dirty environment the filter should be checked regularly. 10 Troubleshooting If the problem keeps occurring, please contact Care of Sweden or your local distributor. Problem Solution The control unit does not Check that the power supply has been connected to the mains supply.
11 Technical specification CONTROL UNIT SPECIFICATION Model CuroCell® iA Automatic, CuroCell® iA Manual Input voltage 100-240 V / 50-60 Hz / 0,6 A Output voltage 12 V DC Power supply Ungrounded AC outlet, Use only power supply with P/N electrical safety class II WR9QE1500LRPCIMG3138 Power consumption Max 18 W...
80/85/90/100/105/120 x 200/210 12,5 kg (80x200 cm) x 20 cm Note: Care of Sweden reserves the right to modify the product specification at any time. 11.1 Standards The system is tested and approved according to the following European standards where applicable requirements are met.
11.2 Symbol key Symbols to convey medical device information CE-marked in accordance with Medical Device Manufacturer Regulation (EU) 2017/745 Medical Device Distributor Date of manufacture Symbols for traceability and product information Item number SN-number Type BF Class II Equipment (double IP class (Enclosure class) insulated).
• If it is assessed that the product is or could be contaminated (e.g., used by patients with a known bloodborne infection), the product must be handled in accordance with the healthcare provider’s or local authority’s procedures for contaminated waste. 12.3 Returns Contact Care of Sweden or your local distributor before returning the product.