STIHLER ELECTRONIC ASTOFLO PLUS ECO User manual

Instructions for use
Warmer for Blood, Intravenous
Fluids and Irrigation Fluids
REF AFP300
REF AFP302
STIHLER ELECTRONIC GmbH • 70597 Stuttgart • Germany
Part No. 10038.12Rev. 05 10/2017

To be filled in by the user:
Serial number
Registration number
Device location
Start-up date
Manufacturer:
STIHLER ELECTRONIC GmbH
Julius-Hoelder-Strasse 36
70597 Stuttgart
GERMANY
Tel. [phone]
Fax [phone]
www.stihlerelectronic.de
E-Mail: [e-mail]
© 2017 STIHLER ELECTRONIC GmbH
STIHLER ELECTRONIC GmbH, Stuttgart, declares in sole responsibility that this
product (230 –240 VAC models only) conforms to EC Directive 93/42/EEC on
medical devices.
Notified body: DEKRA Certification GmbH, registration number 0124.

Contents
1 Information about these Instructions............................................................................5
2 General information ........................................................................................................5
2.1 GUARANTEE CONDITIONS.................................................................................................5
2.2 LIABILITY........................................................................................................................5
2.3 DISPOSAL OF THE EQUIPMENT ..........................................................................................6
2.4 RETURN OF A USED PRODUCT ..........................................................................................6
2.5 SERVICE INFORMATION....................................................................................................6
3 Important safety information..........................................................................................7
3.1 DANGERS ......................................................................................................................7
3.2WARNINGS.....................................................................................................................7
3.3 CAUTIONS....................................................................................................................11
3.4 NOTICES......................................................................................................................12
4 Specification of application..........................................................................................12
4.1 INTENDED USE..............................................................................................................12
4.2 INTENDED MEDICAL INDICATION ......................................................................................12
4.3 CONTRAINDICATIONS.....................................................................................................13
4.4 POSSIBLE ADVERSE EFFECTS.........................................................................................13
4.5 INTENDED PATIENT POPULATION .....................................................................................13
4.6 INTENDED USER PROFILE ...............................................................................................13
4.7 INTENDED USE/OPERATION ENVIRONMENT .......................................................................13
4.8 INTENDED PART OF THE BODY/TYPE OF TISSUE.................................................................13
5 Symbols .........................................................................................................................14
6 Product description.......................................................................................................16
6.1 INTRODUCTION .............................................................................................................16
6.2 TECHNICAL DESCRIPTION...............................................................................................16
6.3 COMPONENTS OF THE ASTOFLO PLUS ECO...............................................................19
6.4 CONTROL PANEL...........................................................................................................21
7 Operating states............................................................................................................23
7.1 STANDBY MODE............................................................................................................23
7.2 ON MODE.....................................................................................................................24
7.3 HEATING MODE.............................................................................................................25
7.4 INCREASING/DECREASING THE SET TEMPERATURE OF THE HEATING PROFILE ......................26
7.5 CHANGING THE BRIGHTNESS OF THE DISPLAY...................................................................27
8 Installation .....................................................................................................................28
8.1 INITIAL START-UP ..........................................................................................................28
8.2 INSTALLATION OF THE WARMER ......................................................................................28
9 Getting started...............................................................................................................29
9.1 PREPARATION FOR USE .................................................................................................29
9.2 PRIMING,INSERTING THE INFUSION LINE AND STARTING THE INFUSION ................................31
9.3 AFTER USE...................................................................................................................33
9.4 CLEANING AND DISINFECTING.........................................................................................34

10 Alarms and troubleshooting.......................................................................................36
10.1 LOW TEMPERATURE ALARM..........................................................................................37
10.2 OVERHEATING ALARM..................................................................................................38
10.3 CABLE BREAK ALARM...................................................................................................39
10.4 SELF-TEST ALARM.......................................................................................................40
10.5 CONNECTION ALARM ...................................................................................................41
10.6 STANDBY MODE -FAILURE............................................................................................42
10.7 ON MODE -FAILURE ....................................................................................................42
11 Brief overview of operating states and alarms.........................................................43
11.1 OVERVIEW OF OPERATION STATES................................................................................43
11.2 OVERVIEW OF ALARMS ................................................................................................44
12 Maintenance.................................................................................................................45
12.1 RECURRENT TESTS.....................................................................................................45
12.2 SET UP FOR ELECTRICAL SAFETY TESTS ........................................................................52
12.3 TEST PROTOCOL.........................................................................................................53
13 Technical data..............................................................................................................55
14 Conformity with international standards...................................................................56
15 Ordering information and accessories......................................................................57
16 Guidelines and manufacturer's declaration..............................................................58

1 Information about these Instructions
ASTOFLO PLUS ECO Instructions for Use
5
1 Information about these Instructions
Carefully read the entire instructions for use before using the
device.
Correct and safe operation can only be guaranteed if the
instructions for use are observed.
Incorrect use can result in damage to the product or to other
property and/or personal injury.
Keep the instructions for use for future reference.
Only use the device for the intended purpose as described in
these instructions for use. Refer to chapter 4 Specification of
application.
2 General information
2.1 Guarantee conditions
The guarantee period is 12 months. During this guarantee period the manufact-
urer will repair or replace free of charge all defects caused as a result of material
or manufacturing errors.
Other damage is not subject to this guarantee. The guarantee does not include
cases of misuse or incorrect handling, use of force, or damage caused by normal
wear and tear. This applies also to changes undertaken by persons who are not
authorised by the manufacturer and to modifications to the original condition.
If the equipment is damaged during the guarantee period, send the cleaned
equipment to the nearest sales point or directly to STIHLER ELECTRONIC
GmbH. The sender is responsible for any transport and packaging costs.
2.2 Liability
The manufacturer is only liable for the safety, reliability and performance of the
equipment
if all operating, servicing, and calibration procedures have been carried out by
trained and qualified persons according to the procedures published by the
manufacturer;
if only original spare parts have been used to replace components as needed;
if assembly and repairs are only carried out by authorised personnel or an
authorised service centre;
if the electrical installations satisfy the locally applicable regulations and the
IEC/EN requirements and
if the equipment is used for its intended purpose and at a suitable location in
accordance with the instructions for use.

ASTOFLO PLUS ECO Instructions for Use
2 General information
6
2.3 Disposal of the equipment
Electrical devices are recoverable waste and should not be disposed of in
domestic waste at the end of their service life. Please follow the local rules for the
disposal of used products, or send the cleaned and disinfected equipment with a
corresponding note to STIHLER ELECTRONIC GmbH or your closest sales point.
This will ensure the most cost efficient and proper disposal of your old equipment.
2.4 Return of a used product
A report must be sent together with the equipment, detailing the precise reasons,
circumstances, and, if known, the cause of the return. To prevent transportation
damage, the equipment should be shipped either in the original packaging or in
other, well-protected packaging.
WARNING
Risk of infection!
Clean and disinfect the equipment after every use and before you return the
equipment for repairs.
NOTICE
The customer is responsible for the proper packaging and labelling of returns.
2.5 Service information
For service or technical support, please contact your local sales point or the
following:
STIHLER ELECTRONIC GmbH Tel. [phone]
Julius-Hoelder-Strasse 36 Fax [phone]
70597 Stuttgart www.stihlerelectronic.de
GERMANY E-Mail: [e-mail]
Follow the national regulations on the disposal of medical products.

3 Important safety information
ASTOFLO PLUS ECO Instructions for Use
7
3 Important safety information
These instructions for use define and refer to the following safety information.
DANGER
DANGER indicates a hazardous situation which, if not avoided, will result in
death or serious injury.
WARNING
WARNING indicates a hazardous situation which, if not avoided, could result in
death or serious injury.
CAUTION
CAUTION indicates a hazardous situation which, if not avoided, could result in
minor or moderate injury.
NOTICE
NOTICE indicates a property damage message.
3.1 Dangers
DANGER
Risk of explosion!
Do not use the ASTOFLO PLUS ECO in an environment at risk of explosion or
in the presence of flammable anesthetics.
3.2 Warnings
WARNING
Risk of injury!
Use of the ASTOFLO PLUS ECO must be carried out under the supervision
of a physician.
Read and observe all instructions, stickers, and accompanying documentat-
ion enclosed with the medical device. Failure to observe the instructions,
including warnings and safety information, can result in incorrect handling,
patient injury, injury to users or medical personnel, damage to the device, or
material damage.
Operate and service this equipment only in accordance with the procedures
described in these instructions and with the applicable standards, rules, and
guidelines. The manufacturer shall not be responsible for the safety of users
or patients if any actions/procedures other than those published are carried
out during operation, servicing, or recurrent tests.

ASTOFLO PLUS ECO Instructions for Use
3 Important safety information
8
WARNING
Risk of injury!
This device may only be operated by appropriately trained and medically
qualified healthcare professionals.
The service personnel must be appropriately trained and qualified.
Do not use the ASTOFLO PLUS ECO until the following error conditions have
been remedied through appropriate corrective action:
- Damaged or worn cables, plugs, or connecting socket.
- Damaged housing, damaged or loose control panel.
- Control unit has been exposed to mechanical impact / exposed to severe
shock or exposed to liquid.
- Alarm without knowing the cause.
- Damaged heating profile, e.g. caused by clamps, scissors or improper
handling or storage.
- Damaged or missing markings/safety signs/warnings on the control unit
and/or heating profile.
If the yellow "Alarm” LED and the acoustic alarm signal are not activated
automatically when the device turns on by pressing the "Standby”button”,
remove the device from service immediately.
In the event of an overheating alarm proceed as outlined below:
1. Ensure that the ASTOFLO PLUS ECO safety system has deactivated the
heating function and that the temperature is dropping below 43C. If the
temperature is not dropping, stop the treatment to prevent fluid from
returning to the patient. Remove the applicable tubing immediately from
the heating profile. Further evaluation should be carried out by qualified
medical personnel such as a physician before blood in the line can be re-
infused.
2. Consider the possible reasons for the alarm. For further information see
chapter 10 Alarms and troubleshooting. If in doubt, do not continue
using the warmer.
The mains cable should not touch the patient and should not hinder the
treating personnel.
The ASTOFLO PLUS ECO does not contain any parts the user can repair.
Therefore, do not attempt to repair the ASTOFLO PLUS ECO yourself.
Contact your local sales point.
Any repairs (such as, but not limited to, changing the power supply cord) to
the equipment may only be carried out by persons authorized and qualified
by the manufacturer.
Modifications to the device are not permitted.

3 Important safety information
ASTOFLO PLUS ECO Instructions for Use
9
WARNING
Risk of overheating!
Do not insert the blood return line in the wrong flow direction. The flow
direction must be from the control unit to the free end of the heating profile.
The heating profile must hang freely while in use. Do not kink, cover (not
even partially), clamp (for example, with a surgical clamp) or roll the heating
profile.
Do not place the heating profile under or directly beside the patient. Heat
build-up can occur and/or the infusion line can be squeezed off.
Do not kink or clamp the heating profile during storage, to avoid internal
damage.
Do not cool or expose to cool temperatures (e.g. by evaporating disinfect-
ants) the area near the temperature sensors (the last 40 cm of the free end of
the heating profile).
WARNING
Risk of haemolysis!
Make sure that the infusion line is not kinked.
WARNING
Risk of air embolism!
When fluids are warmed up, it is possible that gas may evolve (bubbles form).
Be aware of the potential for air emboli when using a blood and fluid warmer.
Therefore fully prime all filters, lines and disposable sets before starting a
treatment.
Make sure all connections of the complete fluid stream are fixed tightly to
prevent fluid leakages and inadvertent infusion of air into the fluid stream.
Do not warm infusions containing soluted gas (e.g. bicarbonate).
Extreme care should always be taken to ensure that a bolus of air does not
pass to the patient.
WARNING
Risk of infection!
Use aseptic procedures.
Clean and disinfect the warmer after every use and before you return the
warmer for repairs.

ASTOFLO PLUS ECO Instructions for Use
3 Important safety information
10
WARNING
Risk of electric shock!
To avoid the risk of electric shock, this equipment must only be connected to
a supply mains with protective earth.
Do not use mains adapters that interrupt the earth conductor.
Do not open the ASTOFLO PLUS ECO housing.
If several pieces of equipment are combined or connected together (e.g., in
multiple socket outlets), the total leakage currents must not exceed the
allowable limits (refer to the respective national regulations). Observe the
requirements as stipulated in IEC/EN 60601-1 regarding medical electrical
systems.
All electrical installations must conform to the applicable electrical standards
and the specifications defined by the manufacturer.
Before every use, check to make sure that the ASTOFLO PLUS ECO control
unit and the heating profile are undamaged.
The mains plug must be removed from the socket to fully disconnect the
ASTOFLO PLUS ECO from the mains.
WARNING
Risk of radio interferences!
Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is
necessary, this equipment and the other equipment should be observed to
verify that they are operating normally.
Use of accessories, other than those specified or provided by the manufact-
urer of this equipment could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and result in improper
operation.
Portable RF communications equipment (including peripherals such as
antenna cables and external antennas) should be used no closer than 30 cm
(12 inches) to any part of the ASTOFLO PLUS ECO, including cables
specified by the manufacturer. Otherwise, degradation of the performance of
this equipment could result.

3 Important safety information
ASTOFLO PLUS ECO Instructions for Use
11
3.3 Cautions
CAUTION
Risk of injury!
Federal law (USA) restricts this device to sale by or on the order of a
physician.
When fixing the warmer to a mounting device, pay attention to the max. load
to avoid tilting. Using normal infusion stands ASTOFLO ECO PLUS may be
mounted at a height of up to 165 cm. If you use the robust IV pole
ASTOSTAND, the device can be mounted up to a height of 2 m.
Use only approved infusion sets.
Damage to the heating profile can cause overheating, therefore follow the
instructions below:
Only disinfect the heating profile with alcohol-based agents or an approved
disinfectant.
Do not use solutions containing hypochlorite (bleach) for disinfecting the
heating profile.
Do not kink or pull the heating profile excessively.
Do not use any clamps or sharp instruments on the heating profile as
damage to the profile or the infusion line inside may result.
Use narrow plaster strips or other narrow, soft fixation methods (for example
cannula fixation, tube holder or Velcro®) to fix the heating profile.
Do not use cleaning and disinfection procedures which differ from the
procedure described.
CAUTION
Risk of hypothermia!
When ASTOFLO PLUS ECO is used, the patient’s body temperature must be
monitored at regular intervals.
The specified heating performance will only achieved by inserting the infusion
line into the entire length of the heating profile.
The temperature control of the ASTOFLO PLUS ECO controls and monitors
the temperature of the heating profile, but not the patient’s body temperature.
If the ASTOFLO PLUS ECO cannot be started or if the patient's temperature
balance is insufficient, consider the use of alternative warming methods in
order to avoid or reduce hypothermia or to improve the patient's well-being.

ASTOFLO PLUS ECO Instructions for Use
4 Specification of application
12
CAUTION
Risk of needle dislodgement!
The weight of the heating profile pulls on the patient’s infusion line. Carefully
secure the patient’s access against pulling. Attach the heating profile by
suitable methods (e.g. tape, plaster or Velcro®).
CAUTION
Risk of radio interferences!
The essential performance can be lost or degraded due to EM disturbances.
As a result, there is the possibility of hypothermia of the patient.
According the standard IEC/EN 60601-1-2, medical electrical equipment
requires special precautions regarding electromagnetic compatibility (EMC)
and needs to be installed and put into service according the EMC information
provided.
The device/system can cause radio interferences or can interfere with the
operation of devices in the vicinity. Appropriate measures may be necessary,
such as reorienting or relocating of ASTOFLO PLUS ECO or shielding.
3.4 Notices
NOTICE
To avoid damage to the warmer:
- Do not immerse the control unit or the heating profile in liquid.
- Do not disinfect the warmer with these methods:
steam (autoclave)
hot air
thermo-chemical cleaning solutions.
- Refer to the specific instructions for use of the disinfectants.
To avoid damaging during storage, place the heating profile loosely around
the control unit and do not kink or clamp it. Use narrow plaster strips or other
narrow, soft fixation methods (for example cannula fixation, tube holder or
Velcro®) to fix the heating profile.
The customer is responsible for the proper packaging and labelling of returns.
4 Specification of application
4.1 Intended use
ASTOFLO PLUS ECO is a warmer for Blood, Intravenous Fluids and Irrigation
Fluids. The application areas include blood transfusions, intravenous fluids,
dialysis, hemofiltration and apheresis.
4.2 Intended medical indication
The warming of medical fluids with ASTOFLO PLUS ECO supports the prevent-
ion and therapy of hypothermia.

4 Specification of application
ASTOFLO PLUS ECO Instructions for Use
13
4.3 Contraindications
There are no known contraindications for warming blood, intravenous fluids and
irrigation fluids.
4.4 Possible adverse effects
When the ASTOFLO PLUS ECO is used as a warmer for return blood flow in a
haemofiltration, haemodialysis or haemodiafiltration device, it must be ensured
that the entire system meets the following:
The highest set temperature (43°C) must be used with care when operating at
low effluent flow rates (below 500 ml/h) for patients who weigh less than 30 kg.
Global positive heat balance and net patient warming may occur. If necessary,
operate the warmer at a reduced temperature setting.
Do not allow the heating profile or the power supply cord to interfere with the
scales, fluid bags or scale hooks.
4.5 Intended patient population
There are no restrictions for the intended patient group.
4.6 Intended user profile
The ASTOFLO PLUS ECO Warmer is to be operated only by medically qualified
and trained healthcare professionals.
4.7 Intended use/operation environment
The warmer may only be used in professional healthcare facilities (e.g.
hospital, emergency care, dialysis, including HF surgical equipment, etc.).
The warmer is not intended for home healthcare environment.
The warmer is reusable, but requires cleaning / disinfection between the
applications.
Appropriate medical hygienic factors must be applied for the use of the
warmer.
The warmer must not be used in an environment at risk of explosion or in the
present of flammable anesthetics.
4.8 Intended part of the body/type of tissue
The warmer is used to warm blood or other medical fluids supplied to the body.
The fluids are physically separated from the warmer by disposable parts (tubes).
During application the heating profile has skin contact.

ASTOFLO PLUS ECO Instructions for Use
5 Symbols
14
5 Symbols
Symbols, used on the Control Panel
Alarm condition if the yellow LED is on
"Standby”button: Changes between Standby Mode and On Mode. The
warmer is in Standby Mode if the blue LED is on.
"Start”button: Switches to the Heating Mode. The warmer is
in Heating Mode if the green LED is on.
SET
"Set”button: Changes the set temperature of the heating profile in 1.0° C
increments.
If the "Set”button and "Test”button is pressed at the same time the
brightness of the display is changed (three steps).
"Test”button: Starts safety tests
Temperature setting range is limited
Where applicable, these symbols appear at the appropriate location on the
warmer, on the packaging, on the identification plate, or in the accompanying
documentation.
Defibrillation-proof type CF applied part in accordance with
IEC/EN 60601-1
IPX 1
Protected from drips under the specified operating conditions
in accordance to IEC 60529.
Refer to instructions for use! / Follow instructions for use!
Caution: Federal US law restricts this device to sale by or on order of a
physician.
General warning sign
Catalogue number
Serial number
Year of manufacture
Manufacturer
Prohibition: Do not cover heating profile –risk of overheating!

5 Symbols
ASTOFLO PLUS ECO Instructions for Use
15
Prohibition: Do not clamp the heating profile –risk of damage and
possible overheating!
Prohibition: Do not disinfect the heating profile with Hypochlorite solution
–risk of damage and possible overheating!
Pay attention to the flow direction of the fluid to the patient - risk of fluid
overheating!
Symbol at the connector for potential equalization according IEC/EN
60601-1.
Electrical devices are valuable products and should not be thrown in
dustbin when they reach the end of their serviceable life.
The device is conform to the MDD 93/42/EEC dated 14th June 1993 for
medical devices. The notified Body DEKRA Certification GmbH (Reg. No.
0124) monitors the quality system of the manufacturer. The CE mark
applies only to the ASTOFLO PLUS ECO Warmer. Disposable parts (e.g.
infusion sets) suitable for use with this device have their own approvals.
75JA
MEDICAL –GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL
SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE
WITH standards
ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012), C1:2009/(R)2012
and A2:2010/(R):2012
CAN/CSA-C22.2 No. 60601-1:2014.
Control No. 75JA
This symbol indicates additional information.
Indicates the temperature range within which the package must be stored
and handled.
Indicates the ambient humidity range within which the package must be
stored and handled.
Indicates the pressure range within which the package must be stored
and handled.
Indicates the upright position of the package.
The package must be kept in a dry environment.
The contents of the package are fragile and must therefore be handled
with care. Do not drop or throw.
Recyclable - Polystrene (acc. GB 18455-2001)
CB
Recyclable - Cardboard (acc. GB 18455-2001)
Acoustic alarm signal
No acoustic alarm signal

ASTOFLO PLUS ECO Instructions for Use
6 Product description
16
6 Product description
6.1 Introduction
ASTOFLO ECO PLUS consists of a control unit and a heating profile.
ASTOFLO ECO PLUS is a device for specific heating of blood and fluids which
are delivered to the patients by transfusion, infusion or irrigation. The warming of
the liquid supports the prevention and therapy of hypothermia during or after
surgery; during longer procedures such as dialysis, hemofiltration, or apheresis
the warming leads to a well-being. The applications of the ASTOFLO PLUS ECO
therefore include transfusion, infusion, dialysis, hemofiltration and apheresis.
The ASTOFLO PLUS ECO Warmer can be used to warm fluids administered to a
patient at low flow rates (0 to 2000 ml/h, i.e. 0 to 30 ml/min), see figures 1 to 3.
Even at very high flow rates ASTOFLO PLUS ECO keeps pre-heated infusions
and fluids to the patient warm.
The heating profile is considered as "applied part" (IEC/EN 60601-1).
6.2 Technical description
During operation of the Warmer heat is transferred from the internal heating wire
to the heating profile. Commercially available infusion sets can simply be inserted
in the flexible groove of the heating profile. The heat from the heating profile is
transferred through the infusion sets to the fluid to be warmed.
The temperature of the heating profile is monitored by a microprocessor control-
led temperature control system and by independent alarm systems designed to
alert the operator to failure conditions and, if necessary, to switch off the heating
process automatically in the event of excessively high temperatures.
During operation, the control panel shows the internal temperature of the heating
profile; this is not equal to the temperature of the medium to be warmed. The
ASTOFLO PLUS ECO neither regulates nor monitors the current temperature of
the medium to be warmed. The temperature of the medium to be warmed
depends on a variety of factors, such as, but not limited to additional factors:
room temperature and ventilation
inlet temperature of the fluid (warmed-up or cold)
flow rate
material of the infusion set (PVC, EVA, PU)

6 Product description
ASTOFLO PLUS ECO Instructions for Use
17
CAUTION
Risk of hypothermia!
When ASTOFLO PLUS ECO is used, the patient’s body temperature must be
monitored at regular intervals.
The specified heating performance will only achieved by inserting the infusion
line into the entire length of the heating profile.
The temperature control of the ASTOFLO PLUS ECO controls and monitors
the temperature of the heating profile, but not the patient’s body temperature.
If the ASTOFLO PLUS ECO cannot be started or if the patient's temperature
balance is insufficient, consider the use of alternative warming methods in
order to avoid or reduce hypothermia or to improve the patient's well-being.
Typical temperature curves are shown in the following figures.
Fig. 1 Typical outlet fluid temperatures at 20°C inlet temperature,
set temperature 43°C, PVC

ASTOFLO PLUS ECO Instructions for Use
6 Product description
18
Fig. 2 WP31 outlet fluid temperatures at 20°C inlet temperature,
set temperature 43°C and different infusion sets.
Fig. 3 WP31 outlet fluid temperature at Set temperature 43°C,
different room and inlet temperatures

6 Product description
ASTOFLO PLUS ECO Instructions for Use
19
6.3 Components of the ASTOFLO PLUS ECO
Fig. 4 ASTOFLO PLUS ECO front
#
Part
Description
1
Screw with Star Grip
For adapting the attachment device to infusion
stands of different diameters.
2
Control Panel
Offers control buttons and indicators
(chapter 6.4 Control panel).
3
Flexible Heating Profile
changeable
Transfers heat from the internal heating wire to
the medium to be warmed via the inserted
infusion line.
4
Power Supply Cord with
Mains Plug
Conveys electricity from the wall power outlet to
the control unit. Pull the mains plug to discon-
nect from supply network.
5
Connection Cable Heating
Profile
Connects the control unit and changeable
heating profile.
6
Adaptor of Heating Profile
Connects the heating profile and cable.
6

ASTOFLO PLUS ECO Instructions for Use
6 Product description
20
Fig. 5 ASTOFLO PLUS ECO back
#
Part
Description
7
Universal Attachment
Device
For secure attachment of the control unit.
8
Clip for Heating Profile
Fixes the heating profile/infusion line.
9
Knurled screw
Protects the device against accidental detaching from
the medical rail.
10
Connector for Potential
Equalization
The purpose of additional potential equalization is to
equalize potentials between different metal parts that
can be touched simultaneously, or to reduce differences
of potential which can occur during operation between
the body, the medical electrical devices and conductive
parts of other objects.
The connection is made by green-yellow insulated leads
(min. 4 mm²) to standardized plug connectors and
receptacles.
When connecting/combining medical electrical
equipment together to a medical electrical system, the
requirements of IEC/EN 60601-1 must be observed.
9
8
7
10