Professional Documents
Culture Documents
You will find details of these service operations in the Repair Manual 400
Premium Series, available only for Penlon trained engineers. For any other
inquiry regarding the service or repair of this product, contact the nearest
Penlon accredited agent:
or contact us directly:
EE. UU.
Penlon Inc.
11515 K-Tel Drive
Minnetonka MN 55434
USA.
Email: customer.service@penlon.com
1) Type of equipment
2) Product Name
3) Serial Number
4) Approximate date of purchase
5) Failure apparent
This manual has been developed to provide the authorized information on The importance of patient monitoring WARNING
the operation, routine use and maintenance checks of the range of the
anesthesia machine Prima 400 Series staff. Anesthesia systems can serve to supply gas mixtures and vapors
that may cause patient injury or death if not checked by a qualified
anesthetist.
The information in this manual is correct at the time of publication.
Penlon Limited policy is the continuous improvement of its products. Based The effects of anesthetic drugs might vary considerably from one
on this policy, Penlon Limited reserves the right to make changes that can patient to another, so that the configuration and monitoring of control
affect the instructions in this manual without prior notice. Staff should be levels anesthesia systems alone do not guarantee complete safety of
familiar with the contents of this manual and the operation of the machine the patient. The system monitors and anesthesia patient monitors are
before using the device. useful for the anesthetist, but are not true clinical monitors, since the
patient's condition also depends on your breathing and functioning of
your cardiovascular system.
Before any system or control device with the anesthesia machine, the user
must check that it operates in accordance with relevant standards.
Page #
2 . PURPOSE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
3 . DESCRIPTION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
..................................................................6
3.7 vaporizers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Four . SPECS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
4.3 flowmeters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
4.9 Environmental. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
5.2.3 flowmeters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
5.3 vaporizers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
5.7 Fan. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
6. USER MAINTENANCE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3. 4
APPENDIX
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37 Labeling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
This anesthesia machine has been manufactured to meet the The information in this manual is preceded by the following words it is
specifications and operating procedures in this manual and / or labels of particular importance:
and warnings that accompany it during verification, installation,
WARNING
operation, maintenance and repair in accordance with these
It implies that there is a possibility of injury to the user or
instructions.
others.
CAUTION
To ensure the safety of this device, it must be controlled and maintained
It implies that there is a possibility of damage to the device or other property.
(at least) as minimum standards described in this manual. In case of
failure or suspected failure, the product should not be used under any NOTE
circumstances.
It indicates points of particular interest for efficient and convenient
operation.
The user must accept responsibility for any malfunction resulting from
non-compliance with the requirements detailed in this repair manual. The reader should pay special attention to the warnings, notices and printed
Additionally, the user must accept responsibility for any malfunctions that may notes throughout the manual.
occur due to any misuse or non-compliance with other requirements detailed
in this manual.
This device and any of its constituent parts must be repaired only in
accordance with written instructions provided by Penlon Limited and should
not be altered or modified in any way without the written approval of Penlon
Limited. The user of this equipment shall be responsible for any damage due
to improper use, maintenance, repair, damage or modifications made by
anyone other than Penlon or its designated agents.
Federal laws of the USA. UU. and Canada restrict the sale and use of this
device to, or on the orders of a licensed physician.
You read and understand the following WARNINGS Y 7. Only vaporizers function compatible interlock Selectatec is
PRECAUTIONS before you use anesthetic apparatus. interbloquearán if installed on a manifold of two or three stations.
WARNINGS
1. This device is designed for single use with nonflammable anesthetic
Installing vaporizers without deadlock enables operation over a
agents. Not to be used with or near inflammable anesthetic
vaporizer at a time.
agents, because of a possible danger of fire or explosion.
8. The breathing system which transports the gases from the
anesthesia machine and removes patient exhaled gases is a vital
part of the anesthesia delivery system.
2. Exterior panels should not be removed by unauthorized and the
device should not be used without these panels staff.
Unauthorized personnel must not attempt to access fuses and 9. Since breathing systems require cleaning and often disenfección are
other electrical components. There is a potential risk of electric not a permanent part of the anesthesia machine and therefore may
shock. not be under the direct control of the manufacturer of the
anesthesia machine. When mechanical ventilation is used, the
patient breathing system must be connected directly to an
3. No need to use oil, grease or other inflammable lubricant fan
overpressure relief valve to prevent the possibility of barotrauma.
anywhere in the vicinity of the distribution components of
medical gas.
13. The machine can not be packaged with more than three major
outlets that can access the operator. There is a risk of excessive
(If this is done, the flow of oxygen will drain through the vaporizer leakage current.
and could result in a gross overdosing when the drain valve is
operated).
15. Before using any machine clinically electrically operated for the
first time, check that the engineering department of the hospital 2. Open cylinder valves slowly to avoid damaging the pressure reducing
has performed a test ground continuity. valves. Ensure that the cylinder valves are open with at least one full
rotation when in use.
16. Before using any additional equipment electrically operated via the
auxiliary power outlets on the machine, check that the additional 3 . Under no circumstances anesthetic agents for cleaning purposes
equipment is properly connected and is grounded through its should be used.
outlet.
Four . After use, always turn off the power supply pipeline gas and / or close
the valves of the gas cylinder.
17. A protective grounding conductor that is missing or defective may
increase the earth leakage currents for the patient in values
5. Anti-hypoxic system mechanical (AHD) device: The oxygen control is
exceeding permissible limits, resulting in ventricular fibrillation, or
restricted to prevent the needle valve is fully closed. This ensures
interference with the pumping action of the heart.
minimum basal oxygen flow. DO NOT attempt to shut off the flow to
zero. Do not overtighten.
13. Connect the COMMS external output only approved using the protocol
provided by Penlon Ltd devices. Contact the Technical Support
Department of Penlon Ltd. for more details.
14. Vaporizers: Read the instruction manual supplied with the vaporizer
prior to clinical use. NOTE
The range has been designed to provide a wide choice of configurations and
accessories, including:
Gas supply
Three gases: oxygen, nitrous oxide and air.
3 .1 General construction
Frame
The machine has a cast aluminum base, extruded aluminum bars, with
aluminum and plastic moldings.
Mobility
four rollers placed with a brake on each. The rolls are 125 mm in
diameter.
Work surfaces
The work surface has high end for holding instruments, blisters, etc.
A removable writing tablet is below the work surface (for Prima 460 models
only).
3 .2 Gas circuit
Cylinder clamps Each individual cylinder or supply pipe is run through a separate gas block.
The clamps are mounted on the back and under ISO standards for Each block has a gas outlet high pressure measurement integrated for
indexed accessories pin. To ensure they are only suitable gas cylinders direct mounting of a pressure measurement and a non-return to prevent
installed, the clamps are designed so that the safety latch can not be backflow of gas valve.
Inputs pipe (1) reduce the pressure of compressed gas supply, and (b) a safety valve,
They can be placed up to three gas inlets pipe mounted on the back. factory set to 517 kPa (75 psi) . This prevents pressure buildup under the
diaphragm, if a leak around the valve seat reduction occurs.
The supply hoses are connected by pipe, not interchangeable, specific screw
threaded joints territory (see section 4.2).
filters Adjusting a secondary regulator for oxygen and nitrous oxide improves
To prevent ingress of dirt gas system, a filter is placed in each clamp the performance of mechanical AHD system. The secondary air supply
cylinder and inlet pipe. regulation helps in stabilizing the flowmeter output.
Indicator
Electronic Flow
O2 N2O Air
Nitrous oxide supply is restored only when the pressure of the oxygen
supply rises above the cutoff value.
The whistle will ring when the pressure dropped to 200 ± 21 kPa (29 ± 3
psig), and continue to sound until the pressure falls to approximately 70
kPa (10 psig). Oxygen consumption of the whistle is about 2 L / min
between sound and silence the other times.
The indicator (1) is placed in the front of the machine and is operated from
the oxygen supply and is shown in green when the power is supplied
according to the operating pressure and will be RED if the pressure fails.
3. 4 mechanical anti-hypoxic device (AHD, 3.4.3 Gear Connection: Control of nitrous oxide
anti-hypoxic device) The gear connects the control knob nitrous oxide with a needle valve internal
oxygen. This ensures that there is always a minimum oxygen concentration
3.4.1 Presentation 30% ± 3%. This ratio is valid for all flow rates.
Anti-hypoxic device (AHD) mechanical module is housed within the flow
meter and controls the relative flow rates of oxygen and nitrous oxide.
3.4.4 Basal oxygen flow
a minimum concentration of 30% oxygen default ± 3% in the mixture of It must be supplied continuously basal oxygen flow for the system to
nitrous oxide / oxygen over the range of flow to prevent delivery of hypoxic function properly.
mixture is maintained.
Simple flow tubes: 100 to 200 ml / min
This basal rate can only turn on and off using the switch gas supply.
CAUTION
Oxygen control is restricted to prevent the needle valve is fully closed. This
one
ensures minimum basal oxygen flow.
DO NOT attempt to shut off the flow to zero. Do not tighten the knob too.
Pressure gauges (50 mm diameter) are located on the front panel under the
bench flowmeter. Air meter is placed between oxygen and nitrous oxide. The
meter positions that are not used, are deleted. All pressure gauges are
colored and labeled with a code to indicate the gases whose pressure.
The Gas supply switch (1) operates on oxygen supply and must be in the
position "ON" [On] for normal operation of the anesthesia machine.
The switch, then, controls the supply of all gases provided with a shutoff
valve actuated by a given level of pressure within the oxygen supply (See
Section 3.3.1).
NOTE
The switch also controls the circuit power AV-S interface, and the electronic
flow indicator (if placed).
3 .6 Flowmeters and Controls 3.6.2 Flow tubes double cascade (with / without
electronic flow indicator)
3.6.1 Conventional flow tubes (with / without
The gas flow through the flow tubes of the double cascade always flows
electronic flow indicator)
through the flow tube under the first. The high flow tube should show no flow
3.6.1.1 flowmeters
until it reaches more than 1 L / min. In higher flows at 1 L / min, the tube
Flowmeters, mounted behind the plexiglass cover on the left of the machine
reading high pressure indicates the flow rate for the gas.
are indexed along to prevent inadvertent, improper installation.
All floats indicate the flow rate in line with the upper surface as shown
above.
3.6.1.2 Flow Controls
Each flow control valve is placed directly below the flow tube assembly
which corresponds with, and in turn, the control knob is a color coded for
controlling gas.
Control knob oxygen flow is physically distinguishable from the other flow
controls for identification to the touch, according to ISO standards. When
placed, the flowmeter is always installed in the internal position in the
flowmeter assembly. These positions are cleared if the air for the machine is
specified.
CAUTION
Needle valves are designed to be sealed with a slight twist and can be
The gas supply switch (Refer 3 4 2) located on the front panel controls the
supply of oxygen and should be in the ON position [ON] for normal
operation of the machine.
No operating mode
If the system can not operate normally, an error message is displayed.
Error Messages
the icon will display "?" when the indicator can not
communicate with the sensor assembly
2
external COMMS
COMMs external interface enables connection with external devices via
RS232 connector (2) on the side panel of the machine.
CAUTION
Connect only approved using the protocol provided by Penlon Ltd devices.
Contact the Technical Support Department for more details.
If the main power supply and battery should fail, the system will continue to
monitor the patient and supplying fresh gas. The gas flow will be indicated in
the total flow flowmeter (See 3 6 4 3)
3
The values obtained are displayed on a color LCD display (2) with
simulated flow tubes representing each individual gas flow. The numerical
2
values shown in L / min under the flow tubes.
NOTE
The operation of virtual flow indicator will be reset if the switch reconfigures
gas supply ON [ON] within the period of 30 seconds.
NOTE
The machine will continue to monitor the patient and supplying fresh gas.
The gas flow will be indicated in the total flow flowmeter (See 3 6 4 3)
3.6.4.6 Alarms
Alarms are indicated by the button / indicator alarm status dual function Alarm status screen (6)
(4).
When an alarm is triggered, the alarm button (4) displays an icon Alarm Off
[Off].
Click the button to cancel the alarm. This will eliminate the alarm condition
B TO
alarm silence
WARNING
Alarms medium and low priority can be muted for up to 120 minutes.
Vaporizers should always be securely mounted, and never used
Alarm Volume
independently. Vaporizers installed separately can tip over
accidentally, resulting in excessive volumes of anesthetic drug
Controlled screen (see below 3.6.4.7). uncalibrated enter the breathing system.
one 2
The battery charge is performed automatically when the power supply Interlock System the rear bar
network of the machine is connected to a "live" main supply. Indicator supply
on / off [on / off] emits a yellow light during charging. 2 one
TO B
NOTE
The period specified backup battery will only be available if the battery
remains fully charged.
If the battery has been left to download its load falling below the LOW The interlocking mechanism comprises a metal slider (1) on the back bar.
BATTERY condition, the device will not work properly until the load rises When each station has an installed vaporizer end, the interlock system
above the level LOW BATTERY. It is necessary to recharge the battery prevents both units are on simultaneously.
completely for fourteen hours.
Illustration and photography shows the vaporizer A "ON [ON]" position. The
interlocking fastener (2) in the vaporizer has moved out and the slider (1) has
moved to the right, to prevent operation of the vaporizer B.
Emptying oxygen
Button drain valve emergency oxygen (2) is marked with "O2 +".
Pressing the button provides a supply of between 35-75 L / min oxygen via
the common gas outlet (1). Release the button allows the spring loaded
valve to return to its normal position.
twenty-one
I indicates On [On] 0
indicates Off [Off]
The supply will be controlled by the ON / OFF [ON / OFF] button (2), which
has a built in circuit breaker. Tagout switch:
I indicates On [On] 0 Indicate
Off [Off]
CAUTION
In the case of malfunction of any device connected to the auxiliary
power outlets, check the circuit breaker is tripped.
A: Off [Off] B: C
Bright C:
Dim light
AB
3.9.4 Battery backup virtual flow indicator
4
In the case of failure of the main power system, backup battery intervenes
automatically and provides power supply to the display unit for 30 minutes
nominal (when fully charged). See also 3.6.4.6.
a) Turn the gas supply switch machine ON [On]. the fan will start.
b) While the machine switch is ON [ON], the fan can be turned off 3.9.6 Monitor and other devices
(OFF) and light (ON), using the On / Off switch [On / Off] fan. The power supply network (or adapter) for a system monitor or other
devices requiring a power supply can be plugged into one of the auxiliary
power outlets on the rear of the machine (See 3.9.2).
c) Turn the gas supply to the OFF [Off] position. the fan will turn off.
CAUTION
When the outputs of auxiliary gas in use on a machine with cylinder supply
only, or if the supply pipe is not in use, check the requirements of the flow
rate and ensure that the cylinders adequate backup available. Oxygen and
air
one
Supply pressure
See section 4.5.
3 12 AV-S Fan
b) While the switch Prima 400 Series is ON [On], the fan can be turned
off (OFF) and lighting (ON), using the On / Off [On / Off] fan switch
(see the user manual from the fan).
c) Turn the gas supply ON [ON]. the fan will turn off.
Refer to the user instruction manual for AV-S for detailed information on
installation and operation.
4 .1 physical dimensions
NOTE:
All data are approximate
Worksurface
Height 86 cm
Size: 58 x 25 cm
Writing tablet: 30 x 22 cm
Top Shelf: 71 x 35 cm
Drawers: 12 x 54.5 x 35 cm
Post mounted mast Bushed to posts 25.4 mm (1 inch) or 22mm (7/8 inch)
4 .2 Gas supply
Input connectors and hoses gas supply pipe specific region in compliance
with the relevant national standards: NIST connectors are for the UK and
Europe DISS connectors are specified for EE. UU. The SIS connectors are
for Australia
4 .3 flowmeters
ranges:
Oxygen: 0 - 10 L / min
Air 0 - 10 L / min
Flowmeter accuracy
The accuracy of the flowmeter tubes is ± 2.5% of full scale reading.
4.3.2 Electronic flow indicator (used with conventional flow tubes) Flow rate
Oxygen 0 - 10 L / min
Air 0 - 10 L / min
Precision
Resolution 50 ml / min
4 .4 Gas Pressures
EE. UU./Canadá/Japón RU
Supply pipe:
Supplies cylinder:
reduced pressure regulator (at a flow of 5 L / +15 kPa 310 kPa / -35 kPa (45 +15 kPa 380 kPa / -35 kPa (55
min) psig +2 psig / -5 psig) psig +2 psig / -5 psig)
Supply pipe: The gas is supplied to pressure supply pipe (see above)
Cylinder supply: The gas is supplied under reduced pressure from the regulator to the cylinder (see below)
Oxygen
Two self-sealing connections in the back of the total flow rate machine: not less
4 .7 Emptying oxygen
The system supplies 35-75 L / min when the button is fully depressed.
4 .9 Environmental
environmental operation
Cleaning Clean the outside surfaces with a dry or damp cloth. Use mild soap or a
disinfectant solution if necessary (see section 6.1).
4 10 Power supply
Supply Input:
Overload protection incorporated within the thermal circuit breaker switch on / off
specification US / CSA 10 A
Cable supply: Cable permanently attached (3 m), with hooks for storage in back
fuses T5AH ceramic 250V (5 x 20 mm) high capacity breaker (Live and Neutral).
Fuse T3.15AH 250V ceramic (5 x 20 mm) high capacity breaker (Live and Neutral in each output)
Power outputs:
US specification machines / CSA: 15 A (nominal): the maximum current depends on the use of internal power
US-specification machines / CSA: 10 A (nominal): the maximum current depends on the use of internal power
fuses T5AH 250V ceramic (5 x 20 mm) high capacity breaker (Live and Neutral in each output)
2. t
Fuse T5AH 250V ceramic (5 x 20 mm) high capacity breaker (Live and Neutral in each output)
Fuse T3.15AH 250V ceramic (5 x 20 mm) high capacity breaker (Live and Neutral in each output)
Battery support: virtual flow indicator only 12 V, 1.2 Ah battery sealed lead acid battery fully charged which provides support face 30
minutes
Electromagnetic compatibility
Premium 400 Series meets the requirements of EN 60601-1-2 (electromagnetic compatibility: tests and requirements)
Operating mode
Continuous
Class 1 classification
Type of protection against electric shock: Class 1
tagout
See Appendix 3
Patient class
All types of patient
Flatatos no residual risks that are carcinogenic, mutagenic or toxic for reproduction.
WARNING
Verifications prior to use must be made before each period of clinical
use.
NOTE
These checks should be complemented by periodic performance tests
and a full service test by a trained by Penlon service on schedule
contained in the Service Manual Prima 400 Series engineer.
These checks do not in themselves ensure the safe use of the device, which
remains the responsibility of qualified mism by the doctor.
Power supply
1. Enchufada
2. Encendida
Breathing system
1. Complete System unobstructed and free of leaks using a test "two bags" (see below)
Fan
1. Operating and configured correctly
2. Refer to the user Penlon fan for instructions on manually checks prior to use
Evacuation
1. Operating and configured correctly
monitors
1. Operating and configured correctly
Equipment airway
1. Full range required, working with spare parts
NOTE:
Record the results of this verification in the patient's record Summary:
Do not forget:
1. auto-inflatable bag
3. resuscitation equipment
Breathing system
1. Complete System unobstructed and free of leaks using a test "two bags" (see below)
Fan
4. Running and configured correctly
5. Refer to the user Penlon fan for instructions on manually checks prior to use
Equipment airway
Full range required, working with spare parts
Suction
Clean and running
NOTE:
Record the result of this check in the patient's record
A machine that works wrongly must be repaired by the relevant qualified personnel before use.
1. Attach the patient end of the breathing system (including the angle piece and filter) or a lung bag test.
2. Set the fresh gas flow at 5 L / min and air out manually. Check that there is no obstruction around the breathing system and the non-return valves move.
Check valve function APL squeezing both bags.
3. Turn the fan to ventilate the test lung. Turn off the fresh gas flow, or reduce it to a minimum. Open and close each vaporizer in turn. There should be
no loss of volume in the system.
Oxygen supply:
1. Attach hose pipe oxygen only. Verify that the meter reading correct This ensures minimum basal oxygen flow. DO NOT
pressure is obtained.
attempt to shut off the flow to zero. Do not tighten the knob
too.
2. Turn on the switch gas supply (1). Verify correct basal flow oxygen is
supplied (see section 4.8).
one
Supply of nitrous oxide:
5. Attach hose pipe Nitrous oxide. Check the meter reading.
Turn on gas supply switch (1). Check for a flow of nitrous oxide
when the needle valve of the flowmeter is operating.
Air supply:
6. Attach hose pipe Air. Check the meter reading.
Check for an air flow when the needle valve of the flowmeter is
operating.
1. Place gas cylinders with their respective clamps, open cylinder valves
one at a time and check the pressure in each meter. NOTE
a) When two cylinders are provided for a single gas, test each separately,
cleaning the pressure after each test by opening valve flowmeter.
2. Make sure all flowmeters remain closed until gas supplies are required.
5.2.3 flowmeters
5.2.3.1 Control Flow
1. Turn on gas supply switch (1).
Only virtual flow indicator: Verify that the display screen (2) is
activated.
one
2. Verify that the correct basal oxygen flow is shown (see section 4.8).
3. Open the valve needle flowmeter nitrous oxide and check oxygen flow
increase.
4. Move valve needle oxygen flowmeter. Verify that the full scale oxygen flow
can be achieved.
6. Operate the control knob flowmeter for other gases (if placed), one at a
time, to check: (a) that is obtainable full scale flow; (B) the flow can be
turned off by a gentle rotation of the knob
3
8. conventional flow tubes dual cascade: Verify that the gas flow passes
through the tube initially low flow until full flow is reached, then through
high flow tube.
3. Set a flow of oxygen 300 ml / min, using the flowmeter control and
checking that the oxygen indicator showing the same flow rate (within
the accuracy range given in section 4.3.2).
2. Allow an oxygen flow of 150 ml / min. Block port opening of the connector
with a finger. The pressure in the system low pressure gas will rise and
displayed on the sphygmomanometer.
1. Verify that all joints are gastight. interbloquearán if the collector installed on a rear bar two or three
stations. Installation of vaporizers possible without Interlock allow
2. Verify level agent vaporizer.
operation over a vaporizer at the same time.
3. Verify that the agent delivery concentrations are correct - use an analyzer
agent.
Always follow the procedures and checklist given in the manual supplied
with the vaporizer, particularly when the vaporizer is filled with anesthetic Interlock System rear bar three stations
agent.
one
b) Verify that the gas connection ports in the vaporizer are aligned with the 4. Verify that the second vaporizer (B) can not be "On [On]" position.
valves in the manifold.
c) Lower the vaporizer carefully until on the manifold and lock the vaporizer
in position by rotating the locking lever towards clockwise to 90 or.
NOTE
Do not use excessive force to block the spray on the collector. This will
result in damage of the locking fastener. CAUTION
To prevent damage to the locking axis, ensure that the gas connection ports
are aligned with the valves in the manifold, and are properly secured, before
adjusting the lock lever. .
5 .4 power supply
3 2
1. Connect the power supply network to the outlet corresponding network.
4. Machines with conventional flow tubes and lighting the flowmeter (4)
verify correct operation (section 3.9.3).
one
3
The connectors for the hose and hose inspiration experación, and the
connector of the reservoir bag are plugs 22 mm. All connectors comply with
ISO 5356/1 standard.
A200SP connections
1. Connector inspiratory
2. Connector expiratory
3. Connector bag
49 8
6. tailpipe APL valve - connect the evacuation system Anesthetic Gas
6 May
NOTE
It should be placed a breathing system that meets approved design
parameters selected by the qualified physician.
The system components are not part breathing machine but the
connections between the machine and the breathing system must be
verified as follows:
3
1. Connect a patient circuit inspiratory connector (1) and the expiratory
connector (2) in the absorbent, and a breathing bag connector arm of
the bag (3).
3. Close valve adjustable pressure limiting (APL) (5), and plug the
connection port patient in the patient circuit. Press the drain valve of
oxygen in the front of the machine briefly. Verify that the reservoir bag 2
is inflated and the manometer (6) indicates about 40 cmH2O.
5. If this test fails, recheck the low pressure system on the machine
(section 5.2.4).
If the low pressure test on the machine is successful, check the
fan and the absorbent, at the instruction manual corresponding
user.
The interface wiring is shown to switch on / off the Prima 400 Series and
switch bag / Ventilation A200SP and spirometer.
31
3 25
23 26
2
24
twenty 19 30
18
12
one
17 1528 26 14 4 13 27 16
May
29
12
22 21
7
June
September
2. Control unit fan 19. Gas outlet feed - the fan control unit to the bellows
25. Receptacles input: (i) Absorber Bag A200SP / Position fan control
9. Auxiliary output in the anesthesia machine (Gas supply propulsion)
10. Flow sensor - expiratory (located within the absorbent) (Ii) sensor signal spirometer
11. Flow sensor - inspiratory (located within the absorbent) 26. interface connections on Prima 400 Series and A200SP
WARNING
Do not connect a drain system directly to the absorbent APL valve. It
must be filed with a receiving system control function of positive and
negative pressure.
5 .7 Fan
Fan AV-S 1
b) While the switch Prima 400 Series is ON [On], the fan can be turned
off (OFF) and lighting (ON) using the switch On / Off [On / Off] fan.
WARNING
These components act to effectuate failure of oxygen delivery and are the
main alarm system, operated only by the supply of residual oxygen, as
described in section 3.3
The system can be checked each time the system low pressure oxygen
is pressurized first rotating connecting a cylinder or a pipe.
A formal test (including the action of internal gas cutoff device) will be
used:
2. Set switch gas supply (2) ON [ON]. Set a flow of 2 L / min in both flow
meters.
3. Disconnect the oxygen supply wall outlet or closing the cylinder valve
and check oxygen:
b) the nitrous oxide flow is cut off completely before the oxygen
flowmeter show that the flow is zero.
C) that the display (1) changes to red before the oxygen flow has
completely stopped.
d) air, to be placed, flowing.
NOTE
All gases should be included in the verification prior to use.
b) Care should be taken not to allow liquids to penetrate the closed areas
All other maintenance and service must be performed only by
could result in serious damage to equipment. CAUTION
trained engineers Penlon.
6 .2 absorbing A200SP
CAUTION
The absorbent assembly weighs approximately 15 kg (empty). Removal and
placement again should only be performed by qualified service technician.
When the absorbent rises or take it to hand, always support the weight of the
unit from below the base. Do not lift the absorbent grasping any components
attached to the manifold block (1). CAUTION
The reservoir (2) may contain condensates. Before removing the absorbent
assembly mounted on the pole, refer to the User Manual for instructions
A200SP draining the tank and removal of absorbent.
2. See User Manual A200SP and disconnect all hoses connectors and
cable.
3
2
3. Loosen the knob (3) and lift the assembly of the
absorbent assembly in the post.
Calibration
The system must be calibrated by a trained by Penlon as part of the Service
Schedule detailed in the Technical Service Manual for this device engineer.
6 .4 Service schedules
APPENDIX 1
NOTE
Removal / replacement of the battery should be carried out only by a trained technician.
APPENDIX 2
WARNING approved
accessories
Use only approved accessories Penlon Ltd.
International sales
Tel: + 44 1235 547001
Fax: + 44 1235 547021
E-mail: international.sales@penlon.com
U.S
Penlon Inc. 11515
K-Tel Drive Minnetonka
MN 55434 USA.
APPENDIX 3
tagout
Button drain valve emergency oxygen Off [Offline] (connected to the mains supply)
Tagout, continued
low battery alarm low or medium priority. Battery in use and there are 10
minutes or less remaining battery backup.
Low priority: 10 to 3 minutes remaining, and has recognized the power loss: Medium
priority:
Battery very low. (Red background) high priority alarm. Battery in use and there are
30 seconds or less remaining battery backup.
Loss of mains power. Medium priority alarm. Acknowledge this alarm to continue the low
priority alarm "On Battery" (above), which indicates that more than 10 minutes of backup
are available.
Low priority. More than 3 minutes backup available: Medium priority: No backup
available: (NOTE: battery backup available only if there are more than 3 minutes
available).
APPENDIX 3
tagout
Volume - Alarm
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