4.2 Final Test........................................................................................................................................24
5.6 Components List FOR AM 5000/5..................................................................................................34
SIARE is used throughout this manual as an abbreviation for
Via Giulio Pastore, 18 - 40056 Crespellano (BO) - ITALY
Manufacturer of the equipment described in this manual
P.N.: DU5506130Page 2 of 34Rev.: 3.0
Warning
SIARE HOSPITAL SUPPLIES S.r.l.
Tel.:+39- 051/969802
Fax: +39-051/969101
AM5000 – AM5000/3 – AM5000/5
Service Manual
1. USE OF SERVICE MANUAL
!
1.1 Users of Manual
This manual is strictly for use by SIARE technicians or qualified technicians authorized by SIARE:
The technician authorized by SIARE has available the appropriate tools and spare parts and is trained with
regards to the safety of the product.
SIARE declines all responsibility with regards to technical assistance to the unit without formal authorization
of SIARE.
The correct and safe use for the patient and the operator of the unit, requires the knowledge of the
instructions and advice written in this manual and the User’s manual.
1.2 Description of use
The symbol
the safety of the patient and operator.
The manual describes the unit and its operation with the help of electrical and pneumatic diagrams.
The User’s manual is an integral part of this manual, and the technician should have available a copy of the
User’s manual and should known its contents before performing any of the operations described in this
manual.
placed near an instruction, calls the reader’s attention to important information regarding
1.3 Safety Notes
WARNINGS
The unit has been designed and is manufactured in conditions that guarantee the quality of the product and
its components, in order to ensure the maximum level of reliability and the safety of the patient and the
operator.
Therefore its safety is guaranteed only if it is used as per the instructions contained in this manual and the
User’s manual which is an integral and unseparable part of the product documentation for the technical
assistance.
For safety reasons, it is necessary to strictly follow the scheduled maintenance described in the User’s
manual.
The maintenance and the replacement of any parts has to be performed by authorized SIARE service
dealers and only original SIARE parts or parts checked by SIARE should be used.
SIARE is not civically or criminally liable in the following cases:
1)Use in conditions and for reasons not stated or prescribed in this manual.
2)Lack or omission of scheduled maintenance as described in this manual.
3)Maintenance performed by personnel not authorized by SIARE.
4)Use of non original spare parts or spare parts not checked and approved by SIARE.
5)Connection with equipment that is not in compliance with relevant directives in effect.
P.N.: DU5506130Page 3 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
!
Do not use the equipment in the presence of flammable gases.
!
!
In order to avoid risk of explosion this unit should not be used in the in the presence of flammable
anaesthetic gases such as ether of ciclopropane. This unit can operate only with anesthetics that are not
flammable as per the directive relative to the electrical safety of the anaesthesia units.
Do not connect the unit to the patient using conductive antistatic tubes.
Due to the fact that this machine cannot be used with flammable anaesthetic agents, such as ether or
ciclopropane, the use of antistatic patient tubes is not necessary. Since the use of anitstatic tubes can cause
burns when using surgical equipment at high frequencies, their use is not allowed in any administration with
this equipment.
The unit is not approved for use in areas with danger of explosion.
The unit cannot be used in the presence of explosive gases.
Before connecting the unit with other electrical equipment not described in this
manual, check with the manufacturer.
Regarding electro-medical equipment’s general safety, it is important to follow all rules regarding the
interaction between the equipment and the patient, the operator and the nearby environment.
In order to ensure proper and safe use of the equipment it is crucial to follow the instructions in this
manual and the User’s manual and pay attention to the notes furnished in this User’s manual.
In order to use this equipment, it is vital to know all the instructions in this manual.
The equipment should be inspected and the maintenance performed by SIARE authorized personnel
every 6 (six) months. All maintenance performed by SIARE authorized personnel is recorded in the
equipment’s maintenance log.
Every repair should be performed by SIARE authorized personnel. Siare is not liable for direct or
indirect damage to people or things, due to technical assistance by personnel non-authorized by
SIARE or improper use of the equipment, that is to say a use not described in the User’s manual or
technical manual.
In order to repair equipment that is malfunctioning, has defects or is broken, the operator should contact
SIARE or its authorized local service dealer. It is important, when requesting service, to specify the model
and serial number of the equipment.
Use only the recommended accessories.
The use of other accessories is authorized only by a written authorization from SIARE as per the safety
directives in effect.
The equipment’s operation is authorized only in areas that conform to the safety directives in effect.
P.N.: DU5506130Page 4 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
2. MAINTENANCE PROCEDURES
!
2.1 General Information
In order to ensure the safety of the patient and the operator, the unit should undergo an inspection
and test after 800 hours of use or every 6 months, whichever comes first. The inspection and test require a
specific knowledge of the unit, and therefore have to be made by specially trained SIARE authorized
personnel.
The anesthetist or doctor is responsible for the ordinary maintenance of the unit, as described in this chapter.
Cleaning, disinfecting, sterilization and replacement of parts should be done as per the instructions in the
user’s manual in order to avoid damage to the equipment that could also endanger the safety of the patient
and operator.
The components used have been selected after technical and comparative tests in the designing phase of
the machine.
Furthermore, the same components are always tested during the manufacturing cycle in order to obtain the
maximum level of safety and reliability for the operator and patient.
Therefore whenever a part needs to be replaced, it must be an original spare part, which has been checked
and tested by SIARE.
SIARE assumes responsibility for all provisions of the law, if the unit is used and maintained as per the
instructions in this manual and the technical manual. The Technical Assistance Report, signed by the
authorized SIARE technician, is proof of the completion of the scheduled maintenance.
P.N.: DU5506130Page 5 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
3. TECHNICAL DESCRIPTION
ILOST
PQ V
AM5000
ILMNOST
U
P
Q
R
V
I
L
M
N
OST
U
P
QR V
AM5000/3
AM5000/5
W
X
3.1AM5000 AM5000/3 - AM5000/5 anaesthesia module
AM5000 - AM5000/3 – AM5000/5 regulates the supply and concentration of the gas mixture (Air, O2, N2O),
and also supplies it to the anaesthetic gas vaporizer.
It also allows the selection of the gas mixture to be supplied (Air-O2, or N2O-O2) and the enrichment (with
oxygen) of the supplied gas mixture for emergencies. The AM5000 - AM5000/3 – AM5000/5 is also equipped
with the MIX-LIFE device that guarantees a minimum of 25% oxygen in all open-tap conditions.
By using the three gauges located on the front panel, the medical gases supply pressure coming from the
central gas installation can be continuously controlled (precision ± 10%).
The flowmeters permit the measurement of the flow the of the corresponding gases with a precision of ±
10% of the displayed value or ± 1% of the bottom of the scale, by choosing the highest of the two values.
IOXYGEN supply gauge.
LNITROUS OXIDE supply gauge.
MAIR supply gauge.
NSelector switch for AIR / NITROUS OXIDE. This safety device:
avoids the contemporaneous supply of air and nitrous oxide
only the selected gas will be available on the flowmeters.
OOXYGEN BY-PASS key. By pressing this key pure oxygen is released into the anaesthesia circuit with a
flow of approximately 60 l/min.
POXYGEN flow regulator for fresh gases. It opens counter-clockwise.
QNITROUS OXIDE flow regulator for fresh gases. It opens counter-clockwise.
P.N.: DU5506130Page 6 of 34Rev.: 3.0
Front view
AM5000 – AM5000/3 – AM5000/5
Service Manual
The opening of this regulator automatically supplies a flow of oxygen of about 25% of the total mixture.
A
B
D
E
H
G
F
I
AM5000
A
B
C
D
E
H
G
F
I
AM5000/3
AM5000/5
The flow of oxygen can be viewed on flowmeter (S). This safety device (MIX LIFE) avoid the incorrect
administration of hypoxic mixtures.
RAIR flow regulator for fresh gases. It opens counter-clockwise.
SOXYGEN flowmeter (Max flow 12 l/min). In the model for low flows, there is a second flowmeter (W)
with a lower scale of 1 liter.
TNITROUS OXIDE flowmeter (Max flow 12 l/min).. In the model for low flows, there is a second
flowmeter (X) with a lower scale of 1 liter.
UAIR flowmeter (Max flow 12 l/min).
VSelector switch for the exit of fresh gases (BREATHING SYSTEM or TO AND FRO).
Back View
AOXYGEN inlet from the main medical gas installation.
BNITROUS OXIDE inlet from the main medical gas installation.
CCOMPRESSED AIR inlet from the main medical gas installation.
DOXYGEN inlet from the cylinder’s pressure reducer.
ENITROUS OXIDE inlet from the cylinder’s pressure reducer.
FAIR/OXYGEN outlet for the supply of the lung ventilator, of the active scavenging system and the
tracheal aspiration unit.
In optimal conditions these connector supply COMPRESSED AIR.
If there is no COMPRESSED AIR or there is not enough pressure, the unit automatically switches the
distribution to OXYGEN.
These connectors are supplied standard with the machine if the relative accessories are in use
GEmergency OXYGEN outlet.
HExit of fresh gases connector for TO and FRO.
IFRESH GAS outlet for the Breathing System.
P.N.: DU5506130Page 7 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
3.2 The Pneumatic Distributor
3 3
1 2
1 2
2 4
1 2
1 2
2 4
3 2
1 2
3 2
8
1 1
1 2
1 0
6
2 8
9
2
5
1
3
2
1 5
2
1 0
8
3 0
1 2
2 3
2 8
9
2 8
1 0
1 3
1 3
1 4
1 5
1 5
1 6
1 6
1 7
1 7
1 7
1 8
1 81 8
1 8
1 9
1 9
2 02 0
2 1
2 2
2 2
2 9
4 5
2 5
2 6
2 7
O 2
N 2 O
A I R
T O F L O W M E T E R
F R O M
V A P O R I Z E R
A
B
C
D
1
3
4
132
4 4
4 4
4 4
4 4
4 4
NOTE: THE HERE BELOW INDICATED SCHEMES AND THE PROCEDURES, HAVE BEEN UNIFIED
FOR THE THREE MODULES AM5000 – AM5000/3 – AM5000/5.
REMEMBER: DO NOT CONSIDER THE AIR LINE FOR ANAESTHESIA MODULE A 2 FLOWETERS.
Below is the pneumatic diagram which describes the unit:
The main purpose of the pneumatic distributor is to:
1. take the medical gases form the pipeline connections or cylinder connections.
2. monitor the operating pressure (pressure gauges)
3. select the type of mix that should be administered to the patient (gas selector AIR-N20)
4. take the selected gases to the flowmeter box
5. allow the mixed gases to be taken to the patient ventilation system (breathing system)
6. enrich the oxygen mixture in case of need (O2 bypass)
All the supply inlets are protected by a non-return valve, in order to avoid a leak of gas in case there is no
supply.
P.N.: DU5506130Page 8 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
As secondary functions, it allows:
supplies an auxiliary outlet of only oxygen which is automatically closed for connections to reanimation bags
for emergencies,
supplies auxiliary outlet for O2 and Air (Aux outlet Air/O2) for devices such as the lung ventilator, ventury
aspirator, etc...
The auxiliary outlets for Air/O2 supply medical air if it has a pressure higher than that of the oxygen minus
0.5 bar. The non-return valves 18 and 26 are necessary in order to avoid that air and O2 mix due to the
pressure difference between the two gases’ supply.
Each gas cylinder or pipeline supply conforms to the DISS standard in order to avoid mistakes in identifying
the gases.
The gauges have a colored band indicating the range at which there is the correct supply pressure.
The gases supplied to the AM5000 - AM5000/3-AM5000/5 are connected to the flowmeter box in order to
regulate the flows and to mix the gases that are then sent to the anaesthetic gas vaporizers. From these they
are taken back to the AM5000 - AM5000/3-AM5000/5 in to later be sent to the connector for the fresh gas
supply in the patient ventilation circuit. The gases mixed with the anaesthetic can be later mixed with pure
oxygen for enrichment of the mix that can be done by the operator by using the bypass button.
The selector enables using two different types of breathing systems without disconnection between the
tubes: the first is the patient circuit of the breathing system and the second, is the To and Fro, which is used
for manual ventilation of the patient’s breathing apparatus.
P.N.: DU5506130Page 9 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
The following diagram illustrates the connections between the parts described above, in this case a
F
LOW
M
ETERO
AIR2N O
2FL
OWMETERFLOWMETE
R
flowmeter box with three flowmeters.
43
40
32
34
42
36
39
41
40
37
35
38
34
40
VAPORIZER
P.N.: DU5506130Page 10 of 34Rev.: 3.0
AM5000 – AM5000/3 – AM5000/5
Service Manual
FLOWMETER BOX
FLO
WMETERO
SAFETY
VALVE
TO
VAPORIZER
2
N O
REG.
PRESS.
REG.
PRESS.
2FLOW
METER1234FLOW
M
ETERO
AIR
SAFETY
VALVE
TO
VAPORIZER
2
N O
REG.
PRESS.
REG.
PRESS.
2FL
O
WME
T
ERFLOWM
E
TER
11234
Can be used in the two, three and five flowmeter models.
P.N.: DU5506130Page 11 of 34Rev.: 3.0
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