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RESPIRATORY HUMIDIFIER
TECHNICAL MANUAL
Revision C
Fisher & Paykel Healthcare have a policy of continual product improvement and reserve the right to alter
specifications without notice
2 SPECIFICATIONS ..........................................................................................................7
2.1 Mechanical ............................................................................................................................................. 7
2.2 Electrical................................................................................................................................................. 7
2.3 Performance............................................................................................................................................ 7
2.4 Transport and Storage............................................................................................................................. 8
2.5 Standards ................................................................................................................................................ 8
5 TROUBLESHOOTING.....................................................................................................16
5.1 Operational Problems ............................................................................................................................. 16
5.2 See Manual Codes .................................................................................................................................. 17
1.3 DEFINITIONS
NOTE: A NOTE provides important information or explanation of procedures or conditions that may
otherwise be misinterpreted or overlooked.
Caution
A CAUTION statement designates the possibility of damage to this or other equipment if a
procedure is not followed exactly.
WARNING:
A WARNING statement refers to conditions with a possibility of personal injury if a
procedure is not followed exactly.
UL Marking
CE marking
2.1 MECHANICAL
Dimensions: 94 x 154 x 135 mm (without chamber fitted). 2
Weight: 1.7 kg without chamber.
2.0 kg with MR290 filled with water.
2.2 ELECTRICAL
Supply Voltage: 230 V~ (MR810A--)
115 V~ (MR810J--)
100 V~ (MR810G--)
Supply Frequency: 50 or 60 Hz
Supply Current: 0.8 A maximum at 230 V~ (MR810A--)
1.6 A maximum at 115 V~ (MR810J--)
1.8 A maximum at 100 V~ (MR810G--)
Heater-wire: 22 V~ at 30 W
Heater Plate: 150 W
Heater Plate Thermal Cutout: Operates at 93 ± 5 °C
2.3 PERFORMANCE
Note: Performance results obtained at 23 °C ambient temperature.
2 30 to 95 % relative humidity
2.5 STANDARDS
IEC 60601-1:1988, Medical electrical equipment, Part 1: General requirements for safety
(and EN 60601-1, UL 60601-1, CAN/CSA 22.2 No 601.1, AS/NZS 3200.1.0)
IEC/EN 60601-1-2:2001, Medical electrical equipment, 2: Electromagnetic Compatibility
ISO 8185:1997, Humidifiers for medical use - General requirements for humidification systems
3.1 APPLICATION
The MR810 Respiratory Humidifier is designed to heat and humidify respiratory gases delivered to the
patient via a face, nasal, or oral mask. The inspired gas is passed through the chamber of water where it is
heated and humidified. An optional heated breathing circuit (heated via a wire inside the circuit), can be
used to minimise condensate in the breathing circuit and maximise humidity delivery to the patient; this is
recommended.
The MR810 humidifier consists of two heaters: (a) a heater plate which the humidification chamber slides
3
onto, and (b) an optional heater-wire in the breathing circuit.
WARNING:
Ensure probe port caps are inserted into probe ports of the breathing circuit.
Caution is required when delivering gases that are not body temperature saturated.
The use of breathing circuits, chambers or other accessories which are NOT
approved by Fisher & Paykel Healthcare may impair performance or compromise
safety.
Refer to operating instructions for each accessory.
Ensure maintenance of grounding integrity by connection to a hospital grade
receptacle.
Ensure that the humidifier is always positioned lower than the patient’s airway.
Ensure the humidifier is securely mounted.
The operation of high frequency surgical apparatus, short wave or microwave
equipment in the vicinity of the humidifier may adversely affect its function. If this
occurs the humidifier should be removed from the vicinity of such devices.
Visually inspect accessories for damage before use.
Hot surfaces may exceed 75 °C.
Do not use flammable anaesthetics.
Always disconnect supply before servicing.
Caution
The MR810 does not deliver body temperature saturated gases.
Gas source
Heater Wire
Indicator
3 Heated Breathing
Circuit
MR810
Humidifier
Figure 3.1: Typical setup for oxygen therapy using a heated breathing circuit
Gas source
Unheated
Breathing Circuit
Chamber
MR810
Humidifier Heater wire
adapter
Figure 3.2: Typical setup for oxygen therapy using an unheated breathing circuit
See manual
indicator
When the device is turned on, the humidifier performs internal diagnostic checks before initiating normal
control.
WARNING: Even if the MR810 is switched off with the power button, the unit is
still energised. Disconnect the MR810 from the power supply before servicing.
Connecting a heated wire breathing circuit (between 10 and 28 Ω) to the MR810 will automatically initiate
the heater-wire mode of control. The flow detection algorithm starts, and the Heater-wire Indicator in the
heater-wire connector illuminates.
Flow Detection State
3
At power-on the MR810 controls the heater plate to a fixed temperature dependent on the setting (40 °C at
Low, 50 °C at Medium and High). The humidifier monitors the power required by the heater plate to
maintain this temperature. Once the system is stable (about half an hour), the humidifier estimates the gas
flow rate based on the power required. The humidifier then initiates the normal control state. With the
temperature measured by the chamber sensor thermistor, the humidifier can identify the type of chamber
(reusable or single use) being used and control accordingly.
The humidifier applies power to the heater-wire circuit dependant on the ambient temperature and the mode
selected.
Normal Control State
Once the flow has been estimated, the humidifier controls the heater plate to a fixed temperature based on
the estimated flow. The humidifier then continues to monitor the heater plate temperature and power
consumption for changes. Any significant power change (due to a change in flow, chamber run out of water
etc.), will cause the humidifier to switch back to the flow detection state. Small power changes will cause
the humidifier to step the heater plate temperature up or down to compensate for the change.
Mains Voltage Compensation
The humidifier automatically compensates for fluctuations in mains voltage to accurately control the power
being delivered to the heater-wire and heater plate. Compensation is limited to ± 10 % of rated operating
voltage.
Ambient Temperature Compensation
In the heater-wire mode of operation, cold ambient temperatures will cause the humidifier to automatically
increase the heater-wire power, minimising the condensate in the breathing circuit. Conversely for high
ambient temperatures the heater-wire power is automatically reduced.
Ambient temperature compensation is limited to between 18 and 30 °C, as shown in Figure 3.4, effectively
limiting the maximum effect due to ambient temperature compensation.
20
Mode Level
Heater wire power
15
Low
(Watts)
10 Medium
5 High
0
10 20 30 40
Am bient Tem perature (°C)
4.1 CLEANING
The following is the recommended cleaning procedure for the MR810 Respiratory Humidifier. Solutions
listed below have been tested to ensure that no damage will occur with the metal and plastic components of
the humidifier. Cleaning should be performed as required.
1. Disconnect the humidifier from the electrical outlet.
2. Clean the humidifier with one of the following using a damp cloth:
• Normal dishwashing detergent
• Isopropyl alcohol
3. Wipe the humidifier clear of any cleaning residues before use. 4
Caution
DO NOT immerse the humidifier in any liquid. Using other solutions may damage the
humidifier.
5
open circuit). Check the thermistor is working
correctly, replace if necessary.
Ambient thermistor fault (short or open circuit), 6.6
check heater-wire adaptor, replace if necessary.
Chamber Sense thermistor fault (short or open 6.6
circuit), check heater-wire adaptor, replace if
necessary.
Heater-wire relay fault (short or open circuit). PCB 6.4
faulty, service or replace PCB as necessary.
Heater control triac error (Heater-wire triac short 6.4
circuit or heater plate triac open/short circuit).
Service triac circuitry, replace PCB if necessary.
Heater-wire Clip Circuit error. Service the 6.4
hardware clip circuit, replace PCB if necessary.
Failed factory production testing. Device should be
returned to your Fisher & Paykel Healthcare
representative.
6.1 PRECAUTIONS
WARNING:
Even if the MR810 is switched off with the power button, the unit is still energised.
Disconnect the MR810 from the power supply before servicing.
After servicing the humidifier should be electrically safety tested (§ 7), and
performance tested (§ 8), to ensure correct operation.
Ensure case screws are correctly fitted to the product after assembly. Replace the
top case if any screw thread strips.
Caution
The MR810 contains electrostatically sensitive components. Ensure antistatic procedures are
followed when servicing.
6 Do not use excessive force when re-fastening screws. (Refer to Table 6 for correct torque
settings).
WARNING:
Even if the MR810 is switched off with the power button, the unit is still energised.
Disconnect the MR810 from the power supply before servicing.
1. Ensure mains plug has been disconnected from the wall socket.
2. Place the unit upside down and remove the three screws in the bottom cover (refer to Figure 6.1).
3. Pull the case front forward to disengage the two clips, then lift the front of the bottom cover up and
then away (see Figure 6.1). Refer to the exploded diagram (Figure 8.1) for further dis/assembly detail.
Cable clamp
Locating
position on
top case.
WARNING:
Be sure to replace fuses with the correct type and rating, specified in Table 4.
Always replace fuse F3 with a 2 A fast blow type as serious injury could result from
the wrong fuse. Open the case and remove the PCB (refer to § 6.2)
Note: A limited number of MR810AEA units were manufactured with fuse F3 rated at 1.5 A. These units
can be identified by the fuse rating information laser-scribed on the inside of the lower case. For these units
only, F3 must be replaced with a 1.5 A fast blow fuse.
1. Slide the cable clamp up out of the transformer mount and lift it away from the fuses.
2. The fuses can now be accessed. Refer to Figure 6.3 for the location of the fuses and Table 4 for
replacement fuses.
3. Install the PCB and assemble the case (refer to § 6.8).
Fuse F1
Fuse F2
Fuse F3
Table 4: Replacement fuse ratings and part numbers (for single fuses)
Primary
thermistor
connection Heater Plate
protective earth
Secondary thermistor
connection Mains protective
earth
Heater wire adaptor
connection
Heater plate
connection
Cable tie
Thermal cut-out
reset
Heater Plate
mounting
screws
6 NOTE: Heater plate thermistor(s) will be required (part number 095 428 870).
1. Open the case and remove the PCB (refer to § 6.2).
2. Remove the heater plate (§ 6.5.2). Refer to Figure 8.2 for the exploded diagram.
3. Cut the two cable ties securing the thermistors (refer to Figure 6.7).
4. Remove the screw holding the heater plate thermistors (refer to Figure 6.8).
5. Place the new heater plate thermistor and screw it down.
Orientation of
cable tie closest
to Heater Plate
Heater Plate
harness cable
ties
Thermistor
cable tie
Heater
plate
springs
Backing plate
(heater plate
element underneath)
6 10. Install the heater plate back into the case top (§ 6.5.7).
11. Reassemble the PCB and the case (§ 6.8).
Heater plate
spring
Table 10: Part numbers and colour codes of Fisher & Paykel
Healthcare power cables
102 mm
Heater wire
insulation
Power cord
insulation
Cable clamp
37 mm
Cable collet
Flat edge of
button flange
orientated with
rib on case
Button insert
Button flange
6
Light pipe
PCB locator
holes
WARNING: Ensure case screws are correctly fitted to the product. Replace the top
case if any screw threads strip.
8.1 INTRODUCTION
This section outlines the performance testing required for the MR810 as part of the annual maintenance or
after servicing of the humidifier.
If the MR810 is intended to be used with a heated wire circuit, perform the functional check (§ 8.2) and the
Heater-wire Mode Performance check (§ 8.3).
If the MR810 is intended to be used with a non heated circuit, perform the functional check (§ 8.2) and the
non Heater-wire Mode Performance check (§ 8.4).
8 •
Conduct this check if the MR810 is used with heated breathing circuits.
The following test should be performed with either the RT202 kit (using the included MR290 chamber), or
the MR370 chamber and CR140 reusable circuit kit. Other chambers or circuits will give different results.
• The test should be conducted in an ambient temperature of 23 ± 2 °C with no drafts. Do not conduct the
test with a hot heater plate as this can affect the accuracy of the test. Allow the MR810 to cool before
starting.
• Turning the device on/off, changing temperature settings, changing the gas flow, or disconnecting the
heater-wire will require the test to be restarted.
• Allow 1 to 2 hours to complete the test.
Equipment Number
Test Date
Performed By
02 03 15 012345
Year of Month of Day of Serial Number
manufacture manufacture manufacture
MR810
Model Type Voltage Languages Plug Additional details
ALU Italian, Spanish, Portuguese
AGU German, French, Italian
AFU 230 V~ French, German, Dutch Schuko
ARU Russian, Polish, English
ANU Norwegian, Swedish, Finnish
AEA 230 V~ English Only Australasian
AEK 230 V~ English Only UK
C
Figure 8.1: MR810 Exploded Diagram
C
Figure 8.2: Heater Plate Exploded Diagram
WARNING:
The use of other accessories other than those specified may result in increased
emissions or decreased immunity of the equipment.
Verify correct operation if the MR810 is to be used adjacent to other equipment.
< 5 % UT < 5 % UT
(> 95 % dip in UT for (> 95 % dip in UT for
5 seconds) 5 seconds)
Power Frequency 3 A/m 3 A/m Power frequency magnetic fields
(50/60 Hz) magnetic should be at levels characteristic of
field a typical location in a typical
IEC 61000-4-8 commercial or hospital
environment.
Note: UT is the a.c. mains voltage prior to application of the test level.
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and poles
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and
land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the measured field strength in the location in which
the MR810 is used exceeds the applicable RF compliance level above, the MR810 should be observed to
verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the MR810.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
NOTE 1: At 80 MHz and 800 MHz, the separation distance of the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.