Manual de Servicio Fabian Hfo
Manual de Servicio Fabian Hfo
Manual de Servicio Fabian Hfo
Vers. 1.09
fabian HFO
Rev. 1.17
fabian HFO Servicemanual
Version Change
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Manufacturer:
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Table of Contents
1) Preface................................................................................................................. 8
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8.14.4 Internal tubing fabian HFO with blender V2 and manifold V2 ............ 37
8.14.5 Colour coded tubing........................................................................... 38
8.15 HFO Module ................................................................................................ 39
8.15.1 Hardware revision .............................................................................. 39
8.15.2 HFO Board ........................................................................................ 41
8.15.3 HFO pneumatic ................................................................................. 41
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1) Preface
This service manual is intended for use by ACUTRONIC Medical Systems AG trained and authorized
service personnel.
ACUTRONIC Medical Systems AG does not condone or approve of service activity on its products by
other than ACUTRONIC Medical Systems AG trained or authorized personnel and ACUTRONIC
Medical Systems AG is not responsible for any unauthorized repairs or modifications, or any repairs or
modifications made by unauthorized procedures.
Use of the incorrect part, or failure to exercise due care in the installation, removal, servicing, checkout
or calibration of parts and equipment or the use of unauthorized accessories, may result in damage to
the equipment which may in turn result in damage in property and injury (including death) to persons.
The purchaser and installer of these parts shall bear full responsibility and liability for the above.
All maintenance performed within the applicable warranty period must be authorized in advance by a
ACUTRONIC Medical Systems AG service representative in order to retain the warranty status of the
subject unit.
Statements in the operating instructions preceded by words “Warning,” “Caution,” and “Note” carry
special significance. The definitions of these words are as follows:
WARNING !
CAUTION !
NOTE !
Indicates points of particular interest for more efficient and convenient operation.
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The following precautions must be observed whenever a circuit board or an integrated circuit is handled.
Failure to do so may result in serious damage to the fabian.
If any circuit boards are to be stored or transported, enclose them in conductive (anti-static) envelopes
3) Warranty
We warrant that this product is free from defects in material and workmanship and, when properly used, will
perform in accordance with applicable specifications. If within one year after the original shipment it is found
not to meet this standard, it will be repaired, at Acutronic Medical Systems AG option, or replaced at no
charge when returned to an Acutronic Medical Systems AG service facility. Any modification to the
equipment or rework or repair by other than Acutronic Medical Systems AG approved personnel will render
this warranty null and void. Acutronic Medical Systems AG shall not be liable for any indirect, special or
consequential damages, even if notice has been given of the possibility of such damages.
The policy of Acutronic Medical Systems AG is to maintain product repair capability for a period of ten years
after the original shipment and to make this capability available at the then prevailing schedule of charge.
All maintenance performed within the applicable warranty period must be authorized in advance by a
ACUTRONIC Medical Systems AG service representative in order to retain the warranty status of the
subject unit
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4) Maintenance
Fabian HFO is a Neonatal and Infant Ventilator and classified as Il b according all applicable
requirements for Medical Products according 93/42 EWG council of European Union dated June 14th,
1993 for Medical Products.
2.) We recommend obtaining a service contract with ACUTRONIC Medical Systems AG exclusive
distributor in your country.
3.) Repairs and general overhaul on the apparatus may only be carried out by ACUTRONIC Medical
Systems AG Service.
4.) Only original ACUTRONIC Medical Systems AG spare parts may be used for maintenance.
5.) Power connection: The apparatus is to be used only in rooms with mains power supply
installations complying with national standards. The standards laid down in IEC-601/1 Safety for
Medical Electrical Equipment, are applicable for electrically powered equipment.
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The liability for proper function of the apparatus is irrevocably transferred to the owner or operator to
the extent the apparatus has been serviced or repaired by personnel not employed or authorised by
ACUTRONIC Medical Systems AG Service or when the apparatus was used in a manner not
conforming to its intended use.
ACUTRONIC Medical Systems AG cannot be held responsible for damage caused by non-compliance
with the above mentioned recommendations. The warranty and liability provisions of the terms of sale
and delivery of ACUTRONIC Medical Systems AG are likewise not modified by the recommendations
mentioned above.
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6) Revision History
10 HW Revision 10 – 1.0
11 – 1.1 etc.
AA Date of manufacture A – January A - 2012
B – February etc. B – 2013 etc.
0001 Sequential number
20-00101-P to 0.9
Prototype
20-00109-P Prototype
from
1.1
20-00130-S HW upgrade on mainboard for CO2 measurement.
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from 1.4
Mainboard Rev. 2.1
20-00189-S and upgraded equipment
New print on rear panel
New Air and O2 inlet filter
from 1.5 Part..Nr.: 20-01-0088
20-00208-S Cooling air filter in bottom case
New rubber feet ( h=15 mm )
Some Improvements in the inner housing
1.6
from New LCD with LED backlight
20-00304-S – and upgraded equipment Purge flow in Proximal line
20-00354-S
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Always clean and disinfect equipment or equipment components prior to any maintenance – including
when returning the equipment for repair.
Every 6 months
Perform the following work:
Filter (casing bottom), replace if necessary
Every 12 months
Maintenance and safety inspections
Perform the following work:
Check alarm and limit value functions
Check pressure connections
Check electrical connections
Check safety shutdown calibration
Every 4 years
Replace the following components:
Air and oxygen Input filter
Filter (casing bottom)
O2 sensor
Proportional valves. pressurised air / oxygen mixer ( Type MiM or FAS )
Input pressure regulator pressurised air / oxygen
2 pcs. calibration valve
Lithium battery CR2032
HFO Membrane
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Due to the high quality of the battery and environmental reasons a regular
battery replacement is not required.
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8) fabian components
8.1 Manifold Ports
4 HFO port
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Figure without purge flow connection. See chapter 8.14 internal tubing for
more details.
7 HFO port
13 Connector to Mainboard
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7 Loudspeaker
8 Fan
9 Optional ports
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8 Loudspeaker
9 Fan
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PIN
Typ Manufacturer
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8.5.2 24 V DC Connector
Rear panel V1
Plug:
Manufacturer: Binder
Series 680, 2 pin
PIN
1 GND
2 + 24 V DC
Rear panel V2
Plug:
Manufacturer: Binder
Series 680, 4 pin
PIN
1/2 GND
3/4 + 24 V DC
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Power Supply:
Please see also Spare part list fabian HFO for details
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F1 24V connection ( 10 AT FF )
F2 Main fuse ( 10 A FF )
F3 Safety OFF function ( 3 A T )
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1 Pressure regulator O2
2 Pressure regulator Air
3 Gas inlet O2
4 Gas inlet Air
5 Calibration valve O2 ( Oxygen sensor )
6 Calibration valve Air ( Oxygen sensor )
7 Pressure sensor O2
8 Pressure sensor Air
9 Proportional valve O2 ( FAS )
10 Proportional valve Air ( FAS )
11 Bleed Air to HFO Module ( only HFO module < 2.0 )
12 O2 sensor compartment with O2 sensor
13 Bleed gas outlet
14 O2 measurement inlet
15 Patient gas
16 Pneumatic Pressure relief Valve ( nCPAP, 500 ± 100 mbar )
17 Processor port
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2 Processor port
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Installed in blender V2
Installed in blender V1
Both valves have the same function and are compatible to the blender PCB 1.1
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Revision ≥ 2.0
Amplitude max 80 mbar
Trapeziodal spring ( conical )
NO Air bleed
HFO connected to inspiratory port
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1 Connector mainboard
2 Processor port
3 Connector HFO Valve / Air bleed ( only HFO module Rev. < 2.0 )
3 Valve and connector , HFO Air bleed ( only HFO module Rev. < 2.0 )
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16
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The fabian HFO Ventilator uses a basic pneumatic structure that is controlled by two PIC
micro controllers on the main board.
A single board computer (CPU) on the main board provides the user interface and
supervises the pneumatic controllers.
The ventilator can be used in different operating (ventilation) modes that are completely
software controlled.
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Processor programmer:
“ICD 3” “ or “Softlog” Programmer with ICSP Adapter,
Windows PC ( XP or Windows 7 ) with installed MBLAP ( ICD3) or ICP (Softlog) Software for
upgrade the following modules:
- Alarm PIC
- Power board PIC
- Blender PIC
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See Document:
\SETUP\
MANUAL: enables the manual installation, does not read the [CONFIGURATION]
DISPLAYCAL: calls only the display calibration, does not read the [CONFIGURATION]
INSTALLTYPE=
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See Document:
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During repair and troubleshooting it is possible to disable the system and patient
alarms.
From now on ALL alarms are disabled till you press the buttons again or restart the
Unit.
- Philips screwdriver PH 1
- Philips screwdriver PH 2
- Torx Screwdriver TX 20
- Screwdriver size 0.8
- Allen key 4 mm / 8 mm
- Socket key 5 mm & 6 mm
- ESD set
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General note:
Fuses shall be replaced by fuses of the same type and value indicated on fabian only.
ACUTRONIC Medical Systems AG recommends the exchange of fuses by authorised
service personnel only.
The main fuses are located in the fuses compartment of the power entry module at the rear
panel of fabian.
Procedure:
1. Disconnect power cord from machine to avoid electrical shock!
2. With a forceps, open the fuses compartment. Pull out the drawer, which contains the
fuses.
3. Exchange the fuses with fuses of the same type and value.
4. Install the compartment back.
5. Make sure, that the arrow directs to the right side.
6. The correct values for the fuses are indicated on the label above the power entry
module.
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1) Unscrew the 4 mm Allen screw inside the compressed air and oxygen connection.
2) Remove the filter
3) Install a new filter.
4) Install the retaining screw.
The NEW filter Part. No.: 3697 can be used for ALL fabian devices
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Switch on Fabian.
Calibrate oxygen sensor at 21 %Vol. and
100 %Vol.
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1. Replace battery
2. Connect mains power AND gas supply
3. Start fabian and let the fabian run till the battery is fully charged
4. Remove mains power supply
5. Let the fabian run until the unit shuts off
6. Follow steps 2 – 5 one more time
7. Now the battery pack is ready to use
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- Contact problem
8 Hot wire Air AIR : U101, L100, R117,
118, T101, R113
- Contact problem
O2 : U101, L101, R119,
16 Hot wire O2 120, T102, R114
- Blender Flow sensor
- Contact problem
24 Hot wire Air AND O2 U101, L100, L101
- Blender Flow sensor
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12.2.3 Hardware
Message CAUSE
SPI Interface
DIO Interface
COM Interface - NetDCU
PIF Interface - Mainboard
I2C Interface
- Battery
Battery defect - Connection Battery / power
board
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Modification / Description: Change HFO module Rev. < 2.0 ( Amp. max. 60 mbar )
Remove the Top, right and left housing from
fabian HFO
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Modification / Description:
Under certain circumstances it is possible that moisture reaches close to the proximal connector of the
fabian HFO.
To prevent this, the proximal port must be modified.
After the modification a small continous flow from the proximal port to the Y Piece is given.
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13) Calibration
Detailed calibration and test instruction in Document:
Special test procedures and instruments are required to perform the testing.
Only use test instrument which is regularly checked and calibrated by certified calibration service, to
guarantee that they have the required accuracy.
WARNING
Hazardous voltages exist within the ventilator. Always observe appropriate safety
precautions when working on the ventilator while the machine is connected to an
electrical power source to prevent possible accidental injurious electrical shock.
WARNING
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14.1 System
14.1.1 Calibration
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14.1.2 Blenderboard
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14.1.4 Accuboard
14.1.5 Valves
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14.1.6 Display
14.1.7 Settings
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14.1.8 Interfaces
14.1.9 Info
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14.1.10 Licensing
It is also possible to setup the keys via the update USB stick.
The license key (available from Acutronic) must be located in the following directory
on the USB update stick
\ LICENSE
Start fabian in manual update mode.
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See Document:
fabian Test Record
See Document:
fabian HFO Spare parts
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