Operator Manual
25 Pages
Preview
Page 1
Care Essentials
CWS4000 Cocoon Warming System Operator Manual
CONTENTS 1.
OPERATION... 4 1.1.
Unit Setup ... 4
1.2.
Getting Started ... 5
1.3.
Unit Operation Procedure... 5
2.
PATIENT WARMING BLANKETS ... 6 2.1.
Cocoon Disposable Patient Warming Blankets ... 6
2.2.
Cocoon Reusable Patient Warming Blankets... 6
2.3.
Instruction for Use ... 6
2.4.
Practical Issues to Consider When Selecting and Using Blankets ... 7
2.5.
CWS4000 Operating Mode ... 7
2.6.
CWS 4000 Standby Mode ... 8
3.
SYMBOLS ... 9
4.
SAFETY PRECAUTIONS ... 11 4.1.
Danger ... 11
4.2.
Contra-indications ... 11
4.3.
Warning ... 11
4.4.
Caution ... 12
4.5.
Electromagnetic Interference ... 13
5.
PREVENTATIVE MAINTENANCE ... 13 5.1.
Cleaning ... 13
5.2.
Filter Service ... 13
5.3.
Electrical Safety and Performance Inspection ... 13
6.
TROUBLESHOOTING ... 15 6.1.
Warming Blanket Will Not Inflate ... 15
6.2.
Standby Indicator Will Not Light ... 15
6.3.
Equipment Repairs ... 15
7.
ACCESSORIES ... 15 7.1.
Stand ... 15
7.2.
User Training... 15
8.
WARRANTY ... 16
9.
RETURNING OF UNIT FOR REPAIR ... 16 9.1.
Australia ... 16
9.2.
Worldwide ... 16
10.
SPECIFICATIONS ... 17
11.
APPROVALS ... 18
12.
APPENDIX 1. COCOON CWS4000 PRODUCT INFORMATION... 20
13.
APPENDIX 2. COCOON REUSABLE BLANKET WASHING AND FOLDING INSTRUCTIONS ... 22
14.
Appendix 3. Instructions on Placement of Blanket and Multiple Hose Ports ... 24
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INTRODUCTION This device should only be operated under the guidance/supervision of qualified medical/nursing personnel or other paramedical staff trained in the use of Convective Patient Warming Systems. Intended Use The Cocoon Convective Warming System is indicated for hyper or hypothermic patients or normothermic patients for whom induced hyper or hypothermia or localized temperature therapy is clinically indicated. In addition, the Cocoon Convective Warming System can be used to provide patient thermal comfort when conditions exist that may cause patients to become too cold or too warm. The Cocoon Convective Warming System can be used with adult and pediatric patients. It is a pre-requisite for all persons using this medical device to understand the information contained in this Manual. Read and understand this Manual and all precautions prior to operating the Cocoon Convective Warming System. The Cocoon Convective Warming System consists of a CWS4000 and a warming blanket. A connecting hose conducts heated air from the CWS4000 to the warming blanket.
Figure 1 Convective Warming System Care Essentials recommend that a program of regular routine maintenance, electrical safety and performance inspections be instituted for the CWS4000 as described in section 5.3. The CWS4000 is a mains-powered, microprocessor-controlled device that delivers a continuous flow of temperature-controlled air through a flexible hose to the warming blanket. The temperature of the air delivered to the blanket can be set to one of six settings - ambient, 34oC (93.2ºF), 37oC (98.6ºF), 40oC (104ºF), 43oC (109.4ºF), or 46oC (114.8ºF). When a temperature of 46oC (114.8ºF) is selected, the setting automatically drops to 43oC (109.4ºF) after 10 minutes. The CWS4000 will not cool the air delivered to the blanket below the ambient temperature of the room. Air is drawn into the sides of the CWS4000 and passes through a bacteriological HEPA filter. The CWS4000 includes a number of over-temperature prevention systems and in a temperature fault condition it automatically shuts down and signals an alarm. The CWS4000 continuously monitors system integrity and performance from the time of start-up. This Manual presents all the relevant operation information for the Care Essentials CWS4000 Cocoon Warming System. This information is intended for the purposes of operation and maintenance of the CWS4000. It is provided as Commercial-In-Confidence material to the Care Essentials Distributor or CWS4000 owner and shall not be made available to any other organization or person without the specific written permission of Care Essentials. While every attempt has been made to ensure this manual is accurate and complete, no responsibility is taken for any errors or omissions. Care Essentials has a policy of continuous
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product improvement. Product specifications and component types are subject to change without notice. If you, as a user of this manual, have any relevant comments or questions about the CWS4000 or this Manual, your communication with Care Essentials would be welcomed. Our contact details are located on the first page of this Manual.
1.
OPERATION 1.1.
Unit Setup
The CWS4000 may be placed on the floor, mounted on the bed rails of the bed using the bedrail hooks, or clamped to an IV pole using the IV pole clamp. When using an IV pole, do not mount the CWS4000 higher than 1 metre or it could tip over. Do not place the CWS4000 on a bed surface. Note that if the CWS4000 is placed on the floor, increased levels of dust and lint could reduce filter life.
Figure 2 IV pole or stand mounted
Figure 3 Bed rail mounted
Figure 4 Pole mounting height limit
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Figure 5 Operator control panel
1.2.
Getting Started
Plug the mains cable into a conventional, properly earthed mains power socket-outlet and switch it on. The green Standby indicator (B) will illuminate and the CWS4000 will beep when power is connected. Ensure that air is not prevented from entering the inlet slots at the sides by blankets or other objects. Remove the warming blanket from its packaging. Unfold the warming blanket and place it over or under the patient as per the blanket instruction. Connect the air delivery hose to the warming blanket by pushing the plastic fitting into the air inlet port and securing it firmly.
1.3.
Unit Operation Procedure
Select the desired temperature on the control panel by pressing the ambient temperature output button (C) or one of the output temperature selection buttons (E). The appropriate green or yellow light (D or F) will indicate the selected temperature setting. Another temperature may be selected at any time. When using 34oC (93.2ºF), 37oC (98.6ºF), 40oC (104ºF), 43oC (109.4ºF), or 46oC (114.8ºF) temperature settings, place your hand under the warming blanket to confirm that the CWS4000 is supplying warm air. Placement of a blanket, sheet or drape over the inflated warming blanket may be undertaken to maximize the efficiency and minimize the heat loss from the system. When using additional covers it is important to ensure air flow through the convective warming blanket is not disrupted. The internal timer will automatically decrease the temperature setting from 46oC (114.8ºF) to 43oC (109.4ºF) after 10 minutes. This timer can be reset by re-selecting the 46oC (114.8ºF) temperature setting. Switch the unit off by pressing the standby button (A). The green standby indicator (B) will illuminate when the unit is off. The unit will automatically switch off in an alarm condition and the green standby indicator (B) will illuminate together with the red fault alarm indicator (H). In the event that the fault alarm indicator (H) illuminates, disconnect the CWS4000 from the patient. Check the power supply connection from the mains as well as the plug connecting to the machine. Then switch the unit QPF 053 Revision 04
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on. If the fault alarm is still illuminating, switch off the unit and have it serviced by trained personnel. The filter status indicator (G) provides the user with information on remaining filter life. This indicator is interpreted as follows: Indication
Description
Steady green indicator
Filter status normal
Steady orange indicator
Filter life has reached 950 hours
Flashing orange indicator Filter life has reached 990 hours Steady red indicator
2.
Filter life has exceeded 1000 hours and requires replacement
PATIENT WARMING BLANKETS
Care Essentials manufactures both Cocoon single-use and reusable (available Australia only) patient warming blankets. Use only patient warming blankets and machines recommended by Care Essentials. Failure to do so may result in thermal injury.
2.1.
Cocoon Disposable Patient Warming Blankets
Features of Cocoon disposable patient warming blankets include:
Warm, soothing, cocooning design.
Single use. This product is not for reuse due to the risk of cross infection.
Universal inlet port ensures hose stays firmly in the blanket.
Latex free.
Sterile disposable blankets also available
Full range of blankets. Refer to www.careessentials.com.au for details.
2.2.
Cocoon Reusable Patient Warming Blankets
Features of Cocoon reusable patient warming blankets include:
Technically advanced smart fabric.
Antistatic and non-linting.
Oil and water repellent.
Universal air inlet is designed for ease of use and offers a secure fitting to all convective warming machines.
Cocoon reusable blankets are an environmental friendly alternative to disposable blankets.
Full range of blankets: refer www.careessentials.com.au for details. This is a reusable product, which should be laundered between patient uses as per the provided washing instructions with blankets. Care Essentials will review the blankets, with the intention of removing them from use, two years following the date of issue.
2.3.
Instruction for Use
Select the correct style and size of blanket.
Insert and secure the convective warming machine hose into the inlet port. Ensure hose is well inserted and tied on the indicator “TIE HERE”
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Where possible place the convective warming blanket directly patient’s skin. Ensure to touch the white side of the blanket to the patient.
Follow the convective warming machine instruction for use.
Do not use head cover unless patient is intubated and ventilated.
Monitor the patient carefully at all time while using convective warming.
2.4.
Practical Issues to Consider When Selecting and Using Blankets
Select the correct style and size of blanket.
If using a sterile blanket, ensure package is not damged/opend. Check expiry date.
Ensure the CWS4000 delivery hose is attached securely.
Secure the position of the blanket on the patient using tapes and ties.
Place the convective warming blanket directly against the patient’s skin.
When using additional covers over the patient, e.g. sheets, blankets or drapes, it is important to ensure air flow through the convective warming blanket is not disrupted.
Inflate the blanket before adding additional covers.
Monitor the temperature setting on the CWS4000.
In the course of temperature monitoring by clinical staff, if the temperature of the patient is still going down, the CWS4000 should be checked for the performance inspection as per section 3.3 of the Service Manual.
In case the warming through CWS4000 is not found effective, clinicians should consider an alternative warming.
2.5.
CWS4000 Operating Mode
The temperature of the air delivered to the blanket can be set to one of six settings ambient, 34oC (93.2ºF), 37oC (98.6ºF), 40oC (104ºF), 43oC (109.4ºF), or 46oC (114.8ºF) Select the desired temperature on the control panel by pressing the ambient temperature output button or one of the output temperature selection buttons 34oC (93.2ºF), 37oC (98.6ºF), 40oC (104ºF), 43oC (109.4ºF), or 46oC (114.8ºF ). The CWS 4000 will deliver air within the specific temperature range given bellow. Temperature Mode
Temperature of Delivered air
o
34 C
34oC±2oC
37oC
37oC±2oC
40oC
40oC±2oC
43oC
43oC±2oC
46oC
46oC±2oC
Ambient
deliver air to the blanket at the ambient temperature of the room.
When the temperature mode selected, CWS4000 starts functioning as follows:
The green light indicator next to the selected temperature illuminates.
Fan motor operates.
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Heater activation as per temperature settings except ambient mode, when heater does not get activated.
Hour meter connected on the main PCB gets activated.
2.6.
CWS 4000 Standby Mode
Select the standby button to place the unit in standby mode. When in standby mode, the following events occur;
Illuminates standby green indicator light.
Turn off heater & fan
Deactivate hour meter
Alarm and fault detection function remains active.
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3.
CWS4000 Cocoon Warming System Operator Manual
SYMBOLS
The following symbols are used on the Cocoon Convective Warming System:
Follow Operating Instruction
Attention: Refer website or manual
Dangerous voltage
Type BF applied part
Do not free hose
Single patient Use
NON STERILE
The device has not been sterilised
STERILE
The device is supplied sterile
Latex free
Keep Dry
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Date of Manufacture
European Authorized Representative European Conformity
Protective earth ground
Fuse
16°C-
Ambient operating temperature range, indoor use only 55°C
Storage Conditions -20°C
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4.
CWS4000 Cocoon Warming System Operator Manual
SAFETY PRECAUTIONS
Review the following safety precautions prior to servicing the CWS4000.
4.1.
Danger
Explosive hazard. Do not use in the presence of flammable anaesthetic agents.
Risk of electric shock. Disconnect mains power before servicing the CWS4000.
4.2.
Contra-indications
The 46 degree Celsius setting is not recommended for patients who are non-responsive or with impaired circulation.
Device is only to be used by or under the advice of healthcare professionals.
4.3.
Warning
To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
Do not apply heat to lower extremities during aortic cross clamping. Thermal injury may occur if heat is applied to ischemic limbs.
No free hosing – use of the CWS4000 without a compatible convective warming blanket may cause thermal injury.
Ensure that no direct or indirect contact is made between the patient and the communications connector located on the rear of the CWS4000.
Do not use other warming devices in conjunction with CWS4000 unless guided by appropriate qualified clinician.
The CWS4000 must only be opened or serviced by qualified personnel such as certified biomedical electronics technicians or certified clinical engineers familiar with repair practices for servicing medical devices, and in accordance with the Service Manual. Damage to the CWS4000 or malfunction could otherwise result.
Ensure the CWS4000 is subjected to the specified routine electrical safety and performance inspections.
The temperature of the patient should be continuously be monitored at a regular interval.
In the course of temperature monitoring by clinical staff, if the temperature of the patient is still going down, the CWS4000 should be checked for the performance inspection as per section 3.3 of the service manual.
In case the warming through CWS4000 is not found effective, senior clinicians should be informed for an alternative warming.
During the use of the CWS4000 Warming System, ensure no excessive pressure is delivered or contacts the user
In the event of excess fluid contact with the CWS4000 it is recommended that the unit be disconnected from the mains power supply and checked by qualified personnel.
Use only in accordance with Operator Manual instructions.
Do not position the CWS4000 so that it is difficult to operate the appliance plug and socket.
Do not lay non-porous peach side of the Cocoon blanket touching the patient. Always lay the porous white side of the Cocoon blanket over or under, touching the patient.
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Only some disposable blankets are supplied sterile, all other disposable and reusable blankets are supplied non-sterile.
Do not use the sterile blanket if the packaging is damaged/opened
Do not use the sterile blanket if the expiry date has passed.
Do not allow the patient to lie on the warming unit hose or allow the hose directly contact the patient’s skin during patients warming, thermal injury may result. No modification of this equipment is allowed. The unit will automatically switch off in an alarm condition and the green standby indicator will illuminate together with the red fault alarm indicator on the front key pad. To avoid injury, do not use the CWS4000 patient warming system for therapy, unless the CWS4000 system is free from mechanical damage, mounted securely or safely placed on a hard surface. Do not use material of good conductivity such as water, gel and other similar substances underneath the blanket. If used, it will lead to decrease of effectiveness of warming. If a transient high surge of electrical voltage comes though the machine, the machine may go into fault mode evidenced with fault alarm and fault indicator. The machine can be reset by switching off and switching on. Then the machine is ready for further use. Patient is not the intended operator of this device and patient is not to service or maintain the device. Do not undertake service of the device while in use.
4.4.
Caution
Operate the CWS4000 only in the specified supply voltage range as detailed in Section 10 below or on rear label on the machine.
When using an IV pole, do not mount the CWS4000 higher than 1 metre or it could tip over.
Use only with 5 wheel base IV pole with atleast 2 wheels with breaking padels and maximum height of 1m.
Monitor the temperature and cutaneous response of patients who are incapable of reacting, communicating and/or who are without a sense of feeling according to institutional protocol. Monitor the patient’s vital signs regularly. Adjust air temperature or discontinue therapy when the therapeutic goal is reached or if vital sign instability occurs. Notify physician of vital sign instability immediately.
Do not leave paediatric patients including infants unattended during therapy.
It is not recommended that the unit be operated with a filter, which has exceeded the specified life period.
It is recommended to avoid keeping the machine on stand-by mode for long periods, to the extent possible.
Federal US law restricts this device to sale by or on the order of a physician.
To reduce the risks associated with environment contamination, follow applicable regulations when disposing this device along with accessories or any of its electronic components.
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4.5.
CWS4000 Cocoon Warming System Operator Manual
Electromagnetic Interference
The CWS4000 has been designed to comply with IEC 60601-1-3rd Edition (Medical electrical equipment – Part 1: General requirements for safety. 2. Collateral standard: electromagnetic compatibility – Requirements and tests) but this does not guarantee that other equipment in the vicinity will not be affected by the electromagnetic emissions from the CWS4000. Similarly, other equipment in the vicinity may affect the operation of the CWS4000. It is recommended that all equipment used near the CWS4000 comply with the relevant electromagnetic compatibility requirements for that equipment and to check before use that no interference is evident or disruptive. Increasing the distance between offending devices, and keeping interconnecting leads as short as possible will help reduce the effect. There is no essentail perforamance for CWS4000 for the purpose of EMC.
5.
PREVENTATIVE MAINTENANCE 5.1.
Cleaning
Do not immerse the device or hose while cleaning. Moisture will damage the components and thermal injury may occur.
Do not use a dripping wet cloth to clean the device. Moisture may seep into the electrical contacts and damage the components.
Do not use alcohol or other solvents to clean the labels of the device, strong solvents may damage the labels and other plastic parts.
Disconnect the device from the power source before cleaning.
Clean the CWS4000 control panel, enclosure exterior, and hose with a soft cloth lightly dampened with a non-staining hospital disinfectant or mild detergent or antimicrobial spray
Dry with separate soft cloth.
Clean accumulated dirt and lint from the air inlet slots using a vacuum cleaner.
If, after cleaning, there is any visible deterioration of components, device surface or hose, it is to be replaced.
5.2.
Filter Service
Only qualified service personnel may change filters. Refer to the CWS4000 Service Manual for instructions on replacing the filter. Under normal use, replace the HEPA filter inside the CWS4000 every 1000 operating hours or 12 months, whichever occurs first. The filter status indicator (G) will warn of the need for filter replacement.
5.3.
Electrical Safety and Performance Inspection
Care Essentials recommend that the CWS4000 receive regular electrical safety inspections. Information on the type and frequency of inspections may be obtained from locally published technical standards. In Australia, the relevant technical standards are: AS/NZS 3551 Technical management programs for medical devices. This standard specifies procedures required to develop equipment management programs for medical devices. Some of these include procedures for acceptance, fault management and
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routine testing of medical devices. This standard specifies electrical safety, essential safety and performance testing. AS/NZS 2500 Guide to the safe use of electricity in patient care. This standard provides a comprehensive guide to the safe use of electrically operated equipment used in health care facilities. Measures are detailed to provide and maintain patient and operator safety, including details of the classes of equipment and electrical installations to be used for particular medical procedures. Programmed electrical safety inspections are essential to confirm continued operator and patient safety. Mandatory, statutory requirements for electrical safety inspections may also apply. Care Essentials also recommends that the CWS4000 receive at least an annual performance inspection as described in the CWS4000 Service Manual. As a minimum electrical safety inspection & performance inspection should be performed annually. The temperature limit thermostat test is optional and may be performed at the discretion of those resposible for the technical management of the CWS4000.
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6.
CWS4000 Cocoon Warming System Operator Manual
TROUBLESHOOTING 6.1.
Warming Blanket Will Not Inflate
Make sure the CWS4000 is plugged in to an energized mains power socket-outlet.
Check both ends of the delivery hose for proper connection.
Check the delivery hose and warming blanket inlet for kinks.
Check that there are no obstructions to the air inlet slots.
In case of a multi-port blanket, it is possible that both the ports may be opened inadvertently. In that case, change the blanket.
Check the warming blanket for damage. If air is flowing from the hose, try another warming blanket.
Request qualified service personnel check for a clogged or dirty filter.
Check for fault alarm.
6.2.
Standby Indicator Will Not Light
Extremely high storage temperatures (such as those found motor cars on hot summer days) can cause the temperature limit thermostats in the CWS4000 to actuate. Should this occur, the standby indicator (B) will fail to light when the CWS4000 is connected to mains power. If this occurs, simply wait for the CWS4000 to cool down and eventually the thermostats will automatically reset and the standby indicator (B) will light. Request qualified service personnel check for blown mains power fuses.
6.3.
Equipment Repairs
Repairs to the CWS4000 should be performed by qualified personnel such as certified biomedical electronics technicians or clinical engineers familiar with repair practices for servicing medical devices, and in accordance with the CWS4000 Service Manual. Damage to the CWS4000 or malfunction may otherwise result.
6.4 Fault alram and fault indicator is activated 1. The unit should be switched off and within few seconds it should be switched on. 2. Check the power connecting plug at the back of the unit for tight/secure connection. 3. After doing above, if the fault alarm and fault indicator is still illuminating, request qualified/trained service personnel to check.
7.
ACCESSORIES 7.1.
Stand
An optional stand for the CWS4000 is available with or without basket. Please note the trolley stand has not been tested to IEC 60601-1-3rd +A1 Edition.
7.2.
User Training
In-service training is available from Care Essentials or a nominated distributor.
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8.
CWS4000 Cocoon Warming System Operator Manual
WARRANTY
The CWS4000 is warranted free of defects in material and workmanship under normal use and operation for a period of one year, under the terms and conditions of the Care Essentials warranty in place at time of purchase. During the warranty period, Care Essentials will repair or replace at its sole option, free of charge, any defective parts or products returned with prior authorization prepaid to Care Essentials. Consumable items such as filters are excluded. The full warranty is available from Care Essentials upon request. This warranty does not cover products abused, misused, or altered outside the factory. This warranty does not cover the following accessories or consumables; filters, hose covers, power cords, or accessory blankets.
9.
RETURNING OF UNIT FOR REPAIR 9.1.
Australia
Call Customer Service (+61 3 5277 1455) or write to [email protected], to request a Return for Repair. The Cocoon CWS 4000 must be cleaned and disinfected (by wiping over with Chlorhexidine 0.5% in Alcohol 70% solution or any other mild, non-staining disinfectant solution) prior to return to Care Essentials. The Cocoon CWS 4000 must be packaged with suitable packaging to protect the machine in transit. (Preferably the Cocoon carton and foam packaging, as supplied with the machine.) Apply the shipping label addressed to Care Essentials Pty Ltd.
9.2.
Worldwide
Contact your local distributor/supplier/agent for any warranty repair, replacement or parts requirements. For more details about distributor, please write to [email protected].
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10.
CWS4000 Cocoon Warming System Operator Manual
SPECIFICATIONS
ELECTRICAL 220-240 VAC, 50/60Hz
Rated input
110-120 VAC, 50/60 Hz
Supply Power
1100 Watts Maximum 2 x 6.3 Amp 250V Time Lag (T) 5x20mm (220-240 VAC)
External Fuses
2 x HBC 10 Amp 250V Time Lag (T) 5x20mm (110-120 VAC)
Heater
1000 Watt heating element 45 Watt / 230 V
Fan Motor
46 Watts / 115 V
Power Cord
5m
Leakage Current
Meets UL 60601-1 3rd +A1 edition and IEC 60601-1 3rd +A1 Ed requirements
CLASSIFICATION MEDICAL – GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH IEC 80601-2-35, Heating Blankets Pads and Mattresses (2009); (IEC 60601 3rd Edition Affiliated); ANSI/AAMI ES60601-1 (2005+C1+A2); CSA C22.2 No 60601.1 (2008); IEC/EN 60601-1 (2005/2006+C1+C2);
UL Classification
80601-2-35 Heating Blankets Pads and Mattresses (2009) CONTROL NUMBER: E359181 (For CWS4000/110V/120V Unit) Applied Parts
Warming Blanket
Applied Part classification
Type BF
Device classification
Class IIB/Class II
Mode of operation
Continuous
Degree of safety in the presence of flammable Not designed for use in the presence of flammable anaesthetic mixtures anaesthetic mixtures with air/oxygen/nitrous with air/oxygen/nitrous oxide. oxide Surface disinfection is possible using a cloth moistened with a mild, non-staining, disinfectant solution.
Method of disinfection PERFORMANCE
Ambient, 34o±2ºC o
Temperature settings indicate the average air temperature at the end of the delivery hose
(93.2º±3.6ºF),
37 ±2ºC
(98.6º±3.6ºF),
40o±2ºC
(104º±3.6ºF),
43o±2ºC
(109.4º±3.6ºF),
o
46 ±2ºC (114.8º±3.6ºF), Note: The air temperature around the patient is affected by the ambient air temperature, the warming blanket type and the use of an insulating blanket placed on top of the warming blanket. Recommended operating environment is 16ºC ( 60.8 ºF) to 29 ºC ( 84 ºF)
Temperature accuracy of delivered air, except About ± 2oC (±3.6ºF) with delivery hose cover. for the ambient temperature setting Not specified without delivery hose cover. QPF 053 Revision 04
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Environmental conditions required to achieve the specified temperature accuracy
16ºC ( 60.8 ºF) to 29 ºC ( 84 ºF) 30% to 70% relative humidity, noncondensing, maximum altitude of 2000m
Time required to attain the specified temperature accuracy of delivered air following 2 – 5 minutes depending on the blanket models a change in temperature setting including temperature rise from 23±2ºC to 37ºC SAFETY SYSTEMS Dual temperature limit thermostats
Either of two independent 53oC (127.4 ºF) self-resetting thermostats removes power from the CWS4000 if the delivered air exceeds a preset limit temperature.
Heater temperature limit devices
A 98oC(208.4ºF) thermal fuse
Temperature limit alarm
Continuous temperature monitoring guarantees that the temperature of the delivered air maintains its specified accuracy.
Control system failure alarm
Continuous self-monitoring by the control system ensures that it always functions predictably.
PHYSICAL Dimensions
29 cm x 22 cm x 40 cm
Weight
6.0 Kilograms
Enclosure
Flame-Retardant ABS-PC Plastic
Filter type/Life
Bacteriological HEPA filter/ 1000 hours
Storage conditions
-20°C to +55°C (-4°F to +131°F)
Hose engagement with blanket
A tightly engaged blanket with the hose can withstand over 20N force
11.
APPROVALS
The CWS4000 has achieved the following medical device approvals. Certifying Body Wakefield Laboratories Report No. 21977
EMC Technologies Report No. M050325
Title
Standard
Medical Electrical Equipment Part 1: General requirements for safety for CWS 4000/220V-240V
IEC 60601 – 1: 1988 + Amendments 1 and 2 (AS/ NZS 3200.1.0:1998)
Medical Electrical Equipment Part 1: General requirements for safety Section 2. Collateral Standard: IEC 60601 – 1 – 2: 2004 Electromagnetic Compatibility – Requirements and tests for CWS 4000/220V-240V
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Medical Electrical Equipment Part 1: General requirements for safety for CWS 4000/220V-240V
IEC 60601 – 1: 2007
Medical Electrical Equipment Part 1: General requirements IEC 60601 – 1 – 2: 2007 for safety Section 2. Collateral Standard: Electromagnetic Compatibility – Requirements and tests
Care Essentials
for CWS 4000/220V-240V UL International New Zealand 21 Tarndale Grove, Albany Auckland 0632, New Zealand T: +64 9 414 9580 W: ul.com
Medical Electrical Equipment Part 1: General requirements for safety Part A. IEC 60601-1-2:2007 Collateral Standard: Electromagnetic Compatibility AS/NZS 3200.1.2:2005 – Requirements and tests for CWS 4000/110V-120V
UL International New Zealand 21 Tarndale Grove, Albany Auckland 0632, New Zealand T: +64 9 414 9580 W: ul.com
QPF 053 Revision 04
Full Safety Evaluation, including: (UL Classification) (cUL Classification) (Informative Test Report), for CWS 4000/110V-120V
Date 08.03.19
Supersedes: 20.11.2018
Particular Standard - IEC 80601-2-35, Heating Blankets Pads and Mattresses (2009)_ (IEC 60601 3rd Edition Affiliated) ANSI/AAMI ES60601-1 (2005+C1+A2) CSA C22.2 No 60601.1 (2008) IEC/EN 60601-1 (2005/2006+C1+C2) 80601-2-35 Heating Blankets Pads and Mattresses (2009)
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Care Essentials
12.
CWS4000 Cocoon Warming System Operator Manual
APPENDIX 1. COCOON CWS4000 PRODUCT INFORMATION
Model
Care Essentials Pty Ltd, Cocoon CWS4000 (220V-240V/110V-120V)
Where Marketed
Australia, Asia, Middle East, Africa, Europe, North America, South America etc
FDA Clearance
510K Approved
CE Mark
Yes, CE 0805
Configuration
Mobile, portable, pole or bed mounted, trolley
Applications
Operating Theatre, Intensive/Critical Care Area, Recovery, Emergency/Trauma, Ward
Controls
Keypad
Display Type
LED Visual Indicators
Function Indicators
Standby, Filter Status, Fault Indicator, six temperature settings plus ambient setting. Ambient to 46 degrees Celsius
Line Power, VAC
110-120 VAC or 220-240VAC
Warmer Power, W
1100 watts maximum
Blanket
Full range of disposable and reusable types
Hose Length
1.8 metres
Temp Settings
Ambient, 34, 37, 40, 43, 46 degrees Celsius ( 93.2, 98.6, 104, 109.4, 114.8 degrees Fahrenheit)
Safety Thermostats
53 degrees Celsius ±3 degrees Celsius (127.4 degrees Fahrenheit ± 5.4 degrees Fahrenheit)
Automatic Overheat Shutoff
Yes
Alarm Conditions
High temperature safety cut out fuse, visual and audible
Noise Level
<50dB
Warm Up Time
About 2 -5 minutes
Air Flow
38 CFM
Filtration System
Yes, HEPA Filtration
QPF 053 Revision 04 WWWWW
Date 08.03.2019
Supersedes: 20.11.2018
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Care Essentials
CWS4000 Cocoon Warming System Operator Manual
HxWxD
40cm x 29cm x 22cm
Weight
6 kg
Warranty
1 year
Other Specifications
Test port through windows Hyper-terminal communications program
QPF 053 Revision 04 WWWWW
Date 08.03.2019
Supersedes: 20.11.2018
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