Table of Contents
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Manual KanMed Operatherm
Contents
1.
INTENDED USE.......................................................................................................................... 2
2
SAFETY INSTRUCTIONS........................................................................................................... 2
3
TECHNICAL SPECIFICATIONS ................................................................................................. 5
4
DESCRIPTIONS OF FUNCTIONS.............................................................................................. 6
5
USING THE UNIT........................................................................................................................ 9
6
CHECKING OF SAFETY SYSTEMS ........................................................................................ 10
7
ACCESSORIES AND SPARE PARTS ...................................................................................... 11
8
EMC COMPATIBILITY STATEMENT ....................................................................................... 11
9
WARRANTY STATEMENT. ...................................................................................................... 11
10
MAINTENANCE ........................................................................................................................ 12
NOTE:
• Patient warming equipment can harm the patient if not used correctly.
• Never use a unit that do not perform the Self Test according to this manual
• Make sure that the performance of the unit is regularly checked.
• This manual contains important information and must be kept for future reference.
• It is valid for all Operatherm 202 / 200 units.
Manufactured by:
KanMed AB, Gårdsfogdevägen 18B, SE-168 66 Bromma SWEDEN
Tel no: +46 8 564 80 630
0413
Users Manual
KanMed Operatherm 202 /200
Fax no: +46 8 564 80 639
Page
Users instruction
KanMed Operatherm 202
Art. Nr.:OP-202-050 / 5
1
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Summary of Contents for Kanmed Operatherm 202
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Page 1: Table Of Contents
• Make sure that the performance of the unit is regularly checked. • This manual contains important information and must be kept for future reference. • It is valid for all Operatherm 202 / 200 units. Manufactured by: KanMed AB, Gårdsfogdevägen 18B, SE-168 66 Bromma SWEDEN... -
Page 2: Intended Use
Page 1. INTENDED USE The intended use of the Operatherm 202 / 200 is to prevent or minimise heat loss from patients in the Operating Room. The Operatherm must be used in compliance with the instructions in this manual and in accordance to... - Page 3 Manual KanMed Operatherm Page Key switch for temperatures <35ºC and >37ºC Temperature selector switch Alarm silence switch Heating Pad failure alarm Over temperature alarm Control Unit failure Earth potential equalisation connection point 2.3 EXPLANATION OF PICTURES ON THE HEATING PAD...
- Page 4 Operatherm at all. KanMed Gel Pads will achieve a surface temperature that is about 1-2°C lower than the selected Heating Pad temperature. The Gel Pads will also increase the contact surface and thereby increase the amount of heat transferred to the patient 2.8 TEMPERATURE SETTING...
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Page 5: Technical Specifications
Manual KanMed Operatherm Page TECHNICAL SPECIFICATIONS Heating Pad Standard Art. no.:OP-200-002 Voltage 30 Volt DC Power 200 Watt Dimension L 1040 mm W 450mm H 2 mm Weight 2 kg Length of cable 3,5 meter approx. ( Other lengths may be ordered ) -
Page 6: Descriptions Of Functions
Manual KanMed Operatherm Page DESCRIPTIONS OF FUNCTIONS 4.1 THE CONTROL UNIT The Control Unit contains a microprocessor based heating control system that regulates the temperature of each of the 8 (4) elements in the Heating Pad. The temperature is continuously monitored and the average temperature is displayed in steps of 0.5°C by the temperature LED's. - Page 7 Manual KanMed Operatherm Page 4.4 TEMPERATURE INDICATION Selected and actual pad temperature is indicated. The selected value is indicated by a continuously lit LED. Actual temperature - if different from the selected - is indicated by a flashing LED. In case the pad temperature is lower than 32°C or higher than 39°C respective LED will flicker.
- Page 8 Manual KanMed Operatherm Page 4.6.1 HEATING PAD ALARM This alarm will be activated if the pad is not connected, or not properly connected, or if any of the 8 (4) heating elements deviates from normal electrical resistance, or if there is a fault in the connecting cable, in the pad connector or in the regulator power switch.
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Page 9: Using The Unit
Warming Cabinet. A cold Gel Pad will drain heat from the patient during the first 20 -40 minutes. This is the time it takes for the Operatherm to warm a KanMed Gel Pad (with a patient lying on it) to skin temperature. -
Page 10: Checking Of Safety Systems
Manual KanMed Operatherm Page 5.6 ALARMS In case the Operatherm alarms, observe the alarm type indicated and switch the unit off. Try to eliminate the cause for the alarm. Restart the unit and observe a correct self test. In case the alarm comes back without an apparent reason the unit must be checked by a technician. -
Page 11: Accessories And Spare Parts
12 month from the date of purchase. The sole obligation of KanMed with respect to any such defect is limited to the repair with new or re- manufactured parts or, at the discretion of KanMed, replacement of the equipment or refunding of the purchase price. -
Page 12: Maintenance
The supplier will make available on request circuit diagrams, component parts lists, descriptions, or other information which will assist the user's appropriately qualified technical personnel to exchange those parts of the equipment which are designated by the manufacturer as exchangeable. Only the KanMed factory is authorised to perform repairs on the main PCB.