Art. no.: 2.540103 Rev.b *2.

540103*

AT-1 G2
Service Manual
CARDIOVIT

1
 Sales and Service Information
The SCHILLER sales and service centre network is world-wide. Contact your nearest
SCHILLER subsidiary to obtain the address of your local distributor. In case of difficulty,
a complete list of all distributors and subsidiaries is provided on our internet site:

www.schiller.ch

Sales information can also be obtained from:

sales@schiller.ch

Address Headquarters
SCHILLER AG
Altgasse 68
CH-6341 Baar, Switzerland
Web: www.schiller.ch
Phone: +41 (0) 41 766 42 42
Fax: +41 (0) 41 761 08 80
E-mail: sales@schiller.ch

The CARDIOVIT AT-1 G2 bears the CE-0123 mark (Notified Body TÜV-SÜD Produkte Service
GmbH, Ridlerstr. 65, 80339 Munich, Germany), indicating its compliance with the essential require-
ments of the Annex I of the Medical Device Directive 93/42/EE regarding safety, functionality and
labelling. The requirements apply to patients, users and third persons who come into contact with
this device within the scope of its intended use.

Article no.: 2.540103 Rev.b

Issue date: 23.02.18
 CARDIOVIT AT-1 G2 Service handbook

Contents
1 Safety Notes .............................................. 5
1.1 Responsibility of the User ................................................... 5
1.2 Organisational Measures ..................................................... 5
1.3 Intended Use ........................................................................ 5
1.4 Indications for use................................................................ 5
1.5 Contra-indication .................................................................. 6
1.6 Organisational Measures ..................................................... 6
1.7 Safety-Conscious Operation ............................................... 6
1.8 Safety Facilities .................................................................... 7
1.9 Operation with other Devices .............................................. 7
1.10 Maintenance.......................................................................... 7
1.11 Terms of Warranty................................................................ 8
1.12 Safety Symbols and Pictograms ......................................... 8
1.12.1 Symbols used in this document ......................................................... 8
1.13 Symbols used on the device ............................................... 9

2 Overview ................................................. 10
2.1 Main Components of the
CARDIOVIT AT-1 G2 10
2.1.1 Default.............................................................................................. 10
2.1.2 Options............................................................................................. 10
2.2 Keyboard ............................................................................. 11
2.2.1 Description of keys........................................................................... 11
2.3 Display................................................................................. 12

3 Operation ................................................ 13
3.1 Initial operation................................................................... 13
3.1.1 Location............................................................................................ 13
3.2 Connections........................................................................ 13
3.2.1 Back panel ....................................................................................... 13
3.2.2 Right hand side panel ...................................................................... 14
3.2.3 Connection of external cable assemblies......................................... 14
3.2.4 Potential equalisation ....................................................................... 14
3.3 Switching on / off................................................................ 15
Art. no.: 2.540103 Rev.b

3.4 Power supply ...................................................................... 15

3.4.1 Mains and battery indicators ............................................................ 15
3.4.2 Isolating from the mains ................................................................... 16
3.5 Changing the Printing Paper ............................................. 17
3.6 System and ECG settings .................................................. 18

Page 1
 CARDIOVIT AT-1 G2

4 General and System Settings ................19

4.1 System settings .................................................................. 19
4.2 ECG ...................................................................................... 20
4.2.1 Leads & cable .................................................................................. 20
4.2.2 Filters & formulas ............................................................................. 20
4.2.3 Display ............................................................................................. 20
4.2.4 Print formats..................................................................................... 21
4.2.5 PDF Format ..................................................................................... 21
4.2.6 Interpretation.................................................................................... 21
4.3 System ................................................................................. 22
4.3.1 Settings ............................................................................................ 22
4.3.2 Info ................................................................................................... 22

5 Maintenance ............................................23
5.1 Visual inspection ................................................................ 23
5.2 Cleaning the casing and cables ........................................ 24
5.2.1 Cleaning cable assemblies .............................................................. 25
5.2.2 Admissible detergents...................................................................... 25
5.2.3 Non-admissible detergents .............................................................. 25
5.3 Disinfection ......................................................................... 26
5.3.1 Admissible disinfectants................................................................... 26
5.3.2 Non-admissible disinfectants ........................................................... 26
5.4 Cleaning the print head...................................................... 27
5.4.1 Replacing pressure roller print head ............................................... 27
5.5 Battery ................................................................................. 28
5.5.1 Charging the battery ........................................................................ 28
5.5.2 Battery disposal ............................................................................... 28
5.6 Inspection Report ............................................................... 29
5.6.1 Lifed-item replacement every 3 - 5 years......................................... 30
5.7 Accessories and disposables ........................................... 30

6 Trouble Shooting ....................................31

6.1 Possible problems.............................................................. 31
6.2 Preventing electromagnetic interferences ....................... 33
6.2.1 Measures to prevent electromagnetic interferences ........................ 34

7 Software update& Licence key upgrade 35

7.1 Software update procedure ............................................... 35
7.2 Licence key upgrade procedure........................................ 35
Art. no.: 2.540103 Rev.b

8 Unit test and configuration ....................37

8.1 Basic unit test ..................................................................... 37
8.2 Configuration & End test ................................................... 38
8.2.1 Configuration & End test after storage............................................. 38

Page 2
 CARDIOVIT AT-1 G2 Service handbook

9 Technical Data ........................................ 39

9.1 Device .................................................................................. 39
9.2 ECG...................................................................................... 41
9.3 Safety Standards ................................................................ 41
9.4 EMC information ................................................................. 42
9.4.1 Electromagnetic emissions ............................................................. 42
9.4.2 Immunity .......................................................................................... 42
9.4.3 Emissions equipment and systems.................................................. 43
9.4.4 Immunity to proximity fields from RF wireless communications equipment
44
9.4.5 Recommended separation distances............................................... 45

10 Opening housing .................................... 46

10.1 Disassembly AT-1 G2 ......................................................... 46
10.1.1 Replacing battery ............................................................................. 47
10.1.2 Reassembly ..................................................................................... 47

11 Index ........................................................ 49
Art. no.: 2.540103 Rev.b

Page 3
Page 4
CARDIOVIT AT-1 G2

Art. no.: 2.540103 Rev.b

 Safety Notes 1
CARDIOVIT AT-1 G2 Service handbook Responsibility of the User 1.1

1 Safety Notes
This Service Handbook is for qualified service personnel only, trained by Schiller AG.
Refer to the operating instruction manual 2.511235 for operation the device.

1.1 Responsibility of the User

 Specify the competencies of the personnel for operation and repair.
 Ensure that service personnel have read and understood these service instruc-
tions. In particular this section “safety notes" must be read and understood.
 Have damaged or missing components replaced immediately.
 The service personnel is responsible for compliance with all applicable accident
prevention regulations and safety regulations.

1.2 Organisational Measures

 Before servicing the unit, ensure that an introduction regarding the unit functions
and the safety precautions has been provided by Schiller AG
 Keep these service instructions in an accessible place for reference when re-
quired. Make sure that they are always complete and legible.
 Observe the operating instructions and service instructions.
 These service instructions do not override any statutory or local regulations, or
procedures for the prevention of accidents and environmental protection.

1.3 Intended Use

 The CARDIOVIT AT-1 G2 is a 12- lead ECG device intended to be used by
trained medical professionals in healthcare facilities for cardiological diagnosis in
adult and paediatric patients.
 ECG analysis is complemented with algorithms that provide measurement
results, data, graphic presentation and interpretation for review by the user.
Art. no.: 2.540103 Rev.b

1.4 Indications for use

 The CARDIOVIT AT-1 G2 is a 12-lead ECG device intended to acquire ECG
signals from body surface electrodes, and record, analyze, display and print
ECGs for cardiological diagnosis in adult and paediatric patients.

Page 5
1 Safety Notes
1.5 Contra-indication CARDIOVIT AT-1 G2

1.5 Contra-indication
 The unit is not intended for:
• sterile use
• use in potentially explosive areas or in the presence of flammable gases such as
anaesthetic agents.
• direct cardiac application.
• use in an MRI suite.

1.6 Organisational Measures

 Before using the device, ensure that a medical product representative has ex-
plained its functions as well as the safety requirements.
 Keep this user guide in an accessible place for reference purposes. Make sure
that it is always complete and legible.
 Observe the operating and maintenance instructions.
 In addition to this user guide, legal and other binding regulations for the preven-
tion of accidents and for environment protection must be observed.

1.7 Safety-Conscious Operation

 Only operate the device in accordance with the specified technical data.

 © The device is CF classified. It is defibrillation protected only when the

SCHILLER original patient cable is used. However, as a safety precaution and if
possible, remove the electrodes before defibrillation.
 Do not touch the unit during defibrillation.
 To ensure patient safety, none of the electrodes including the neutral electrode,
nor the patient or any person with simultaneous patient contact, must come in
contact with conductive parts, even when these are earthed.
 Immediately report any changes that impair safety (including operating
behaviour) to the responsible person.

Art. no.: 2.540103 Rev.b

 Do not place any liquids on the unit. If liquid is spilled on the device, immediately
disconnect the device from the mains and wipe it. The device must be checked
before reusing.
 Only connect the original SCHILLER patient cable to the patient socket.
 If the patient cable should become defective after defibrillation, an electrode
becomes displaced, or an electrode resistance is too high, a lead-off indication is
displayed in the upper right part of the screen.
 Only use accessories and disposables recommended or supplied by SCHILLER.
The use of third-party accessories (including disposables) may result in injury, in-
accurate information (EMC) and/or damage to the device.

Page 6
 Safety Notes 1
CARDIOVIT AT-1 G2 Service handbook Safety Facilities 1.8

1.8 Safety Facilities

 Operating the device without the correctly rated fuse or with defective cables
constitutes a danger to life! Therefore:
– Do not operate the unit if the earth connection is suspect or if the mains lead,
the power supply unit or the device is damaged or suspected of being damaged.
– Damaged cable connections and connectors must be replaced immediately.
– Electrical safety devices, such as fuses, must not be modified.
– Fuses must only be replaced with the same type and rating as the original.

1.9 Operation with other Devices

 Accessory equipment connected to the analogue and digital interfaces must be
certified according to the respective IEC standards (e.g. IEC/EN 60950 for data
processing equipment and IEC/EN 60601-1 for medical equipment). Further-
more, all configurations shall comply with the valid version of IEC/EN 60601-1.
Everybody who connects additional equipment to the signal input part or signal
output part configures a medical system and is therefore responsible that the sys-
tem complies with the requirements of the valid version of IEC/EN 60601-1. If in
doubt, contact the technical service department or your local representative.
 Any other equipment used with the patient must use the same common earth as
the CARDIOVIT AT-1 G2.
 Special care must be exercised when the unit is used with high-frequency equip-
ment. Use the special high-frequency SCHILLER patient cable to avoid possible
signal interference during ECG acquisition. However, the stimulation units should
only be used at a sufficient distance from the electrodes and both devices must
be connected to the same potential equalisation. If in doubt, the patient should be
disconnected from the device.
 This device can safely be used with pacemaker patients.
 There is no danger when using this device simultaneously with electrical stimula-
tion equipment.
 If the device is part of a medical system, only the original SCHILLER patient cable
must be used with, and connected to, the CARDIOVIT AT-1 G2.
 If the patient cable should become defective after defibrillation, a lead-off indica-
tion is displayed on the screen.
Art. no.: 2.540103 Rev.b

 Portable communication devices, HF radios and devices labelled with the

symbol (non-ionic electromagnetic radiation) can affect the operation of this

device (see page 33).

1.10 Maintenance
 Danger of electric shock! Do not open the device. There are no serviceable parts
inside. Refer servicing to qualified technicians authorised by SCHILLER only.
 Before cleaning and to isolate the mains power supply, switch the unit off and dis-
connect it from the mains by removing the plug.
 Do not use high-temperature sterilisation processes (such as autoclaving). Do
not use E-beam or gamma radiation sterilisation.
 Do not use aggressive or abrasive cleaners.
 Do not, under any circumstances, immerse the device or cable assemblies in liq-
uid.

Page 7
1 Safety Notes
1.11 Terms of Warranty CARDIOVIT AT-1 G2

1.11 Terms of Warranty

Your SCHILLER CARDIOVIT AT-1 G2 is warranted against defects in material and
manufacture, as stated in the Terms and Conditions. Excluded from this warranty is
damage caused by an accident or as a result of improper handling. The warranty en-
titles to free replacement of the defective part. Any liability for subsequent damage is
excluded. The warranty is void if unauthorised or unqualified persons attempt to make
repairs.

In case the device is defective, send it to your local SCHILLER representative or di-
rectly to the manufacturer. The manufacturer can only be held responsible for the
safety, reliability and performance of the device if:

• assembly operations, extensions, readjustments, modifications or repairs are car-

ried out by persons authorised by him, and
• the SCHILLER device and approved attached equipment is used in accordance
with the manufacturer's instructions, and.
• the maintenance intervals as stated in the section EMC information are observed.
There are no express or implied warranties which extend beyond the warranties here-
inabove set forth. SCHILLER makes no warranty of merchantability or fitness for a
particular purpose with respect to the product or parts thereof.

SCHILLER assumes no liability for the loss of data saved on the computer or on the
device. The owner is solely responsible for the data backup.

1.12 Safety Symbols and Pictograms

1.12.1 Symbols used in this document
The safety level is classified according ANSI Z535.4. The following overview shows
the used safety symbols and pictograms used in this manual.

For a direct danger which could lead to severe personal injury or to death.

Art. no.: 2.540103 Rev.b

For a possibly dangerous situation, which could lead to heavy bodily injury or to death.

For a possibly dangerous situation which could lead to personal injury.

For grouped safety notes as listed in this chapter.

Used for electrical dangers, warnings and other notes in regarding operation with elec-
tricity.

Page 8
 Safety Notes 1
CARDIOVIT AT-1 G2 Service handbook Symbols used on the device 1.13

Note For possibly dangerous situations, which could lead to damages to property or
system failure. Important or helpful user information

Reference to other guidelines

Used tool for the following procedure.

1.13 Symbols used on the device

Potential equalisation.

CF symbol. The device is classified safe for internal and external use. However, it is
only defibrillation protected when used with the original SCHILLER patient cable.

Manufacturer symbol, manufacturing date.

The device is IP20-classified and is not protected against the ingress of liquids. Keep
dry.
Symbol for the recognition of electrical and electronic equipment
Equipment/components and accessories no longer required must be disposed of in
a municipally approved collection point or recycling centre. Alternatively, you can re-
turn the equipment to your supplier or the manufacturer for disposal. Improper dis-
posal can harm the environment and human health.

The unit/component can be recycled

Notified Body TÜV-SÜD Produkte Service GmbH, Ridlerstr. 65, 80339 Munich, Ger-
0123
many
Art. no.: 2.540103 Rev.b

Attention: consult accompanying documents.

Consult the user guide.

Mains supply LED

Battery charging status LED (details see Section 3.4.1 Mains and battery indicators,
page 15)

Page 9
2 Overview
2.1 Main Components of the CARDIOVIT AT-1 G2 CARDIOVIT AT-1 G2

2 Overview
The SCHILLER CARDIOVIT AT-1 G2 is a 12-channel ECG unit designed to record,
display, and measure resting ECGs. The display and keyboard enable easy and
intuitive operation to efficiently enter patient data, record ECGs and adjust device
settings.

The CARDIOVIT AT-1 G2 has the following features:

2.1 Main Components of the

CARDIOVIT AT-1 G2
Thermal printer and paper tray LCD screen

Mains/battery status LED

Menu/navigation keys

Setting keys

Art. no.: 2.540103 Rev.b

On/Off key Function keys

2.1.1 Default
• Pacemaker detection
• Manual rhythm printout in real time (channels, speed and amplitude can be
changed)
• Auto mode recording (10 seconds) with user-defined print formats
• Measurements
• Display of all 12 channels (4x3)
• Display of reversed electrodes
• Recording review
• PDF Export

2.1.2 Options
• Interpretation
• CCAA

Page 10
 Overview 2
CARDIOVIT AT-1 G2 Service handbook Keyboard 2.2

2.2 Keyboard

Delete numerical Numerical input

input

2.2.1 Description of keys

Switching the device on/off

Starting an automatic resting ECG

Starting a manual resting ECG

For numerical input: delete (backspace )

• Stopping printout of an automatic/manual ECG

• Closing the menu

Entering patient information. If the key is pressed twice, the previous patient's data
is retrieved.

Printing an ECG from the Preview screen. Unless new patient data has been
entered, additional printouts (copies) can be generated.

Changing the myogram filter (Off, 25, 40 or 150 Hz).

Art. no.: 2.540103 Rev.b

Setting the ECG chart speed and amplitude.

Menu/Enter key and Up/down keys ().

During numerical input, the numbers associated with the keys as well as Backspace
etc. are automatically active.

Page 11
2 Overview
2.3 Display CARDIOVIT AT-1 G2

2.3 Display
The display will vary according to the task being carried out. In all screens, however,
the top and bottom areas always display the same category of information. Example
for a typical ECG view:

Battery capacity/status
(green: mains operation, black: battery operation)
Patient number
Memory Stick detected Date and time

12345 14.03.2017 17.58

Heart rate 60 /min

I
Leads:
Selection with up/down keys ()

II

III

25 mm/s 10 mm/mV LP 150Hz AC 50 Hz

Speed/amplitude
Myogram filter
Notch filter

Menu display and navigation

(1) (1)
Main menu 28.08.2016 17.58
Menu/Enter key to open
(1) (1) (3)

Art. no.: 2.540103 Rev.b

main menu/parameter ECG Patient cable IEC or AHA
Leads & cable >
+
Signals Simultaneous
(1)
(2) Filters & formulas >
Lead sequence Cabrera
Preview >
Stop key to exit a sub-menu (3) Print formats >
(back) and to close the main
menu. Print interpretation >
PDF Export >
SYSTEM
(3)
Settings >

Use the Up/down keys to scroll up or Info (2)

down and select a sub-menu/setting (2)

Navigation help next/previous select close

next/previous select back

change confirm
0..9 input confirm & close menu

Page 12
 Operation 3
CARDIOVIT AT-1 G2 Service handbook Initial operation 3.1

3 Operation
3.1 Initial operation
 Electrical shock hazard. Do not operate the unit if the earth connection is suspect
or if the power supply unit/mains lead is damaged or suspected of being
damaged.

3.1.1 Location
• Do not keep or operate the unit in a wet, moist or dusty environment. Avoid expo-
sure to direct sunlight or heat from other sources.
• Do not allow the unit to come into contact with acidic vapours or liquids.
• The CARDIOVIT AT-1 G2 should not be placed in the vicinity of X-ray or diathermy
units, large transformers or electric motors.

3.2 Connections
 All externally connected hardware must be approved by SCHILLER. Connection
of any hardware not approved by SCHILLER is at the owner‘s risk. Moreover, the
unit's warranty may become invalid.

3.2.1 Back panel

Art. no.: 2.540103 Rev.b

1 2 3 4

(1) Mains connection 100...240 VAC

(2) Potential equalisation stud. The potential equalisation stud is used to equalise
the ground potential of the unit to that of any nearby mains-powered equipment.
Use the hospital or building common ground for all mains-powered units.
(3) USB interface for USB memory stick.
(4) Kensington lock

Page 13
3 Operation
3.2 Connections CARDIOVIT AT-1 G2

3.2.2 Right hand side panel

ECG patient cable connector

 The patient cable as well as the connector comply with the safety standard CF
, e.g. they are fully floating and isolated and defibrillation protected.
 The unit is only CF rated and defibrillation protected if used with the original
SCHILER patient cable.
 In order to prevent disturbance of the ECG signal caused by electromagnetic
interferences:
– only the original SCHILLER patient cable may be used
– the patient cable needs to be screwed on to ensure a secure connection.

3.2.3 Connection of external cable assemblies

1. Connect the mains cable to the mains.
2. Connect the mains cable at the rear of the unit. The mains indicator lamp is lit.
3. Leave the CARDIOVIT AT-1 G2 connected to the mains for 3 hours to fully charge
the battery.
4. Connect the potential equalisation cable.
5. Connect the patient cable (side panel).

Art. no.: 2.540103 Rev.b

3.2.4 Potential equalisation
The potential equalisation stud at the back of the unit is used to equalise the ground
potential of the CARDIOVIT AT-1 G2 to that of all mains-powered equipment in the
vicinity. Use the hospital or building common ground. A yellow/green ground cable is
supplied as an option (article number 2.310320).

 Danger of triggering ventricular fibrillation! If the CARDIOVIT AT-1 G2 is used

together with devices that are designed for direct cardiac application, both
devices must be connected to the hospital/building common ground (potential
equalisation) to prevent equalising currents between different device potentials.

Page 14
 Operation 3
CARDIOVIT AT-1 G2 Service handbook Switching on / off 3.3

3.3 Switching on / off

 The unit is switched on and off with the On / Off key.
To switch the device off, confirm the dialogue by pressing the Enter key.
Turn off device
Do you want to
switch off the
device?

YES NO

The device automatically shuts off, if it is not used for 11 minutes. A dialog will appear

after 10 minutes to prevent automatic shutdown with the key .

3.4 Power supply

3.4.1 Mains and battery indicators
The unit can either be operated by the mains supply or by the built-in rechargeable
battery. Battery charging is indicated by the LED next to the battery symbol.

(1) When the mains supply is connected, the mains LED is lit.
(2) The battery LED is blinking when the battery is being charged, and it is lit when
1
charging is complete.
2
 During battery operation (no mains connected), both LEDs are off.

The status is indicated as follows:

• Battery LED is blinking: the battery is being charged.

• Battery LED is lit: the battery is fully charged.

Art. no.: 2.540103 Rev.b

Battery capacity/charging status indication on the LCD

100% 100%
charging 28.08.2016 17.58
75%
Mains operation
50%
60
• Symbol during mains operation
– Green symbol, filling: battery is being charged
 25% – Green symbol: battery fully charged
• Symbol during battery operation
0% – Black symbol
– Black/red symbol: battery operation, capacity  25%
Battery operation
– Red symbol: battery empty

Page 15
3 Operation
3.4 Power supply CARDIOVIT AT-1 G2

3.4.2 Isolating from the mains

To isolate the device from the mains supply, remove the mains plug from the mains
socket.

Art. no.: 2.540103 Rev.b

Page 16
 Operation 3
CARDIOVIT AT-1 G2 Service handbook Changing the Printing Paper 3.5

3.5 Changing the Printing Paper

Important
The device is delivered without printing paper inserted. The thermal paper is sensitive
to heat, humidity and chemical vapours. The following points apply to both storage,
and when archiving the results:

• Before use, keep the paper in its original cardboard cover. Do not remove the card-
board cover until the paper is to be used.
• Store the paper in a cool, dark and dry location.
• Do not store near chemicals, e.g. sterilisation liquids.
• Do not store in a plastic cover.
• Certain glues can react with the paper. Therefore, do not use glue to attach the
printout onto a mounting sheet.

SCHILLER can only guarantee perfect printouts when original SCHILLER chart paper
or chart paper of the same quality is used.
1. Open the paper tray.

2. Remove the remaining paper.

3. Place a new paper pack into the paper tray with the printed (grid) side facing up-
wards and the black paper mark facing the top of the unit.
Art. no.: 2.540103 Rev.b

4. Pull out the first page as shown on the left.

5. Close the paper tray.

Page 17
3 Operation
3.6 System and ECG settings CARDIOVIT AT-1 G2

3.6 System and ECG settings

• The system settings (time, date, device ID etc.) and other general settings are de-
scribed on page 20.
• The ECG settings are described on page 20.

Art. no.: 2.540103 Rev.b

Page 18
 General and System Settings 4
CARDIOVIT AT-1 G2 Service handbook System settings 4.1

4 General and System Set-

tings
4.1 System settings
The system settings are saved when the main menu is closed.

When the Menu key is pressed, the main menu is displayed. The following illustration
gives an overview of all the settings available.

Main menu 28.08.2016 17.58

ECG Patient cable IEC

Leads & cable > Signals Simultaneous
Filters & formulas >
Lead sequence Cabrera
Preview >
Print formats >
Print interpretation >

PDF Export >

SYSTEM
Settings >
Info

change confirm

1. Press the Menu/Enter key .

2. Select the desired parameter using the keys  (next/previous).
Art. no.: 2.540103 Rev.b

3. Press the key (select) to access the sub-menu.

4. Press the key (select) to access the setting.

5. Use the dual-function keys to enter numerical values, or use the keys 
(change) to select the correct setting.

6. Press the key (confirm) to get to the next parameter.

7. Press the key (back) to return to the main menu.

8. Press the key (close) to return to the ECG screen; the settings are saved.

Page 19
4 General and System Settings
4.2 ECG CARDIOVIT AT-1 G2

4.2 ECG
The default settings are printed bold

4.2.1 Leads & cable

Menu Parameter Description / selection

Patient cable IEC or AHA

Sequential or Simultaneous. If Sequential is selected, consecutive

time segments are used for the individual lead groups (this applies for
Leads & cable
printouts). If Simultaneous is selected, the same time segment is used
Signals
for all lead groups (this applies for printouts). If a print format with a
rhythm lead is defined, Sequential is used, even if you have selected
Simultaneous.

Lead sequence Standard or Cabrera

4.2.2 Filters & formulas

Menu Parameter Description / selection

Notch filter Off/ AC 50/AC 60 Hz

Filters & formulas Myogram filter LP 25 Hz / LP 40 Hz/ LP 150 Hz / Off (250 Hz)

Standard QTc calculation Bazett, Fridericia, Framingham, Hodges

4.2.3 Display
Standard settings for ECG display.

Menu Parameter Description / selection

For Standard:
I / II / III, aVR / aVL / aVF, V1 / V2 / V3, V4 / V5 / V6
Lead group
For Cabrera:
ECG

Art. no.: 2.540103 Rev.b

aVL / I / -aVR, II / aVL / III, V1 / V2 / V3, V4 / V5 / V6
ECG speed 5 / 25 / 50 mm/s

ECG amplitude 5 / 10 / 20 mm/mV

Page 20
 General and System Settings 4
CARDIOVIT AT-1 G2 Service handbook ECG 4.2

4.2.4 Print formats

The stored recordings can be printed in different formats.

Menu Display Description

4 pages (25 mm/s), 8 pages (25 mm/s), 8 pages (50 mm/

ECG printout
s), OFF
Off
4x3 (25 (mm/s)
Print formats Averaged cycles 4x3 (50 (mm/s)
6x2 (50 (mm/s) + 1 rhythm (25 mm/s)
12x1 (25 (mm/s) + 2 rhythms (25 mm/s)
Rhythm lead 1 I, II.....V5, V6
Rhythm lead 2 I, II.... V5, V6
Markings On / Off
Measurements On / Off

10.1.3 PDF Format

Menu Display Description

PDF Export On/Off

4x3 + 1 (25 mm/s), 1 Page
2x6 (25 (mm/s), 1page
ECG Printout
2x6 (50 (mm/s), 1 page
OFF
Rhythm lead I, II.....V5, V6

PDF Format Off

4x3 (25 (mm/s) + 2r (25 mm/s)
Average Cycles 4x3 (50 (mm/s) + 2r (25 mm/s)
6x2 (50 (mm/s) + 2 Rhythm leads (25 mm/s)
12x1 (25 (mm/s) + 2 Rhythm leads (25 mm/s)
Art. no.: 2.540103 Rev.b

Rhythm lead 1 I, II.....V5, V6

Rhythm lead 2 I, II.... V1... V6
Markiings On / Off
Mearurements On / Off

4.2.5 Interpretation
Menu Display Description

Interpretation On / Off
Print interpretation Unconfirmed report On / Off
Abnormal ECG On / Off

Page 21
4 General and System Settings
4.3 System CARDIOVIT AT-1 G2

4.3 System
4.3.1 Settings

To show the setting “Simulation ECG”, type the following key sequence 712.

Menu Parameter

Language Select a language

dd.mm.yyyy, yyyy-mm-dd or mm/dd/
Date format
Settings yyyy.
Date Enter the date
Time (24h) Enter the time

 Enter key sequence 712

Menu Parameter

Settings Simulation ECG Not active/Active

 Do not forget to deactivate the Simulation ECG for normal use.

4.3.2 Info
Software and hardware versions are displayed.

• Device Name
• S/N number
• HW ID
• HW Revision
• SW version
• SW option
• ETM version

Art. no.: 2.540103 Rev.b

• Language

Page 22
 Maintenance 5
CARDIOVIT AT-1 G2 Service handbook Visual inspection 5.1

5 Maintenance
The regular system maintenance must include a software check according to the
manufacturer's instructions. The test results must be recorded and compared to the
values in the accompanying documents.

Maintenance work not described in this section may only be performed by a qualified
technician authorised by SCHILLER AG.

The following table indicates the intervals and responsibilities of the maintenance
work required. Local regulations in your country may stipulate additional or different
inspection intervals and tests.

Interval Maintenance step Responsible

Before each use • Visual inspection of the device and ECG electrodes  User
• Visual inspection of the device
(see page 29, 5.6 Inspection Report)
– LCD display
Every 6 months – Cables and accessories  User
– Power supply unit and mains cable
• Functional tests according to the instructions (see page 29, 5.6
Inspection Report)
 Qualified service
Every 12 months • Safety test according to IEC/EN 62353
personnel

5.1 Visual inspection

Visually inspect the unit and cable assemblies for the following:

 Device casing (not damaged or cracked)

 LCD screen (not damaged or cracked)
 Electrode cable sheathing and connectors (undamaged)
Art. no.: 2.540103 Rev.b

 Mains cable sheathing and connectors (undamaged)

 No kinks, abrasion or wear in any cable assembly.
 Input/output connectors (undamaged).

In addition to the visual inspection, switch on the CARDIOVIT AT-1 G2, scroll through
the menu and test some sample functions. In this way, you can check that:

• the device performs faultlessly

• the display works
• the keyboard works

 Defective units or damaged cables must be replaced immediately.

Page 23
5 Maintenance
5.2 Cleaning the casing and cables CARDIOVIT AT-1 G2

5.2 Cleaning the casing and cables

 Switch the device off before cleaning and disconnect it from the mains by
removing the plug. Do not, under any circumstances, immerse the device in
cleaning liquid and do not sterilise it with hot water, steam or air.

 Do not autoclave the unit or any accessories.

 Do not immerse the device in liquid.
 Do not spray liquid onto the device/cable.
 The use of detergents with a high acid content or detergents that are otherwise
unsuitable can damage the device (i.e. cracks and wear of the plastic casing).
 Always follow the usage instructions provided by the manufacturer of the cleaning
solution.
 With time, the casing may become less resistant:
– if an alcaline cleaner or a cleaner with a high alcohol concentration is left for a
long time on the surface, or
– if a warm disinfectant or detergent is used. Schiller AG therefore recommends
using only cleaning agents that are adequate for sensitive materials such as
plastics, and using them at room temperature (approx. 20°C).
 Never use any of the following solutions or similar products to clean the
equipment: ethyl alcohol, acetone, hexane, abrasive or scouring powder or
material, any cleaning material that damages plastic.
 The patient cable and other cable assemblies must not be exposed to excessive
mechanical stress. Whenever disconnecting the leads, hold the plugs and not the
cables. Store the leads in such a way as to prevent anyone stumbling over them
or any damage being caused by the wheels of instrument trolleys.
 When cleaning, ensure that all labels and safety statements, whether etched,
printed or stuck to the device, remain in place and remain readable.

Thoroughly inspect the device and the accessories before cleaning.

• Look for any signs of damage and make sure that the keys and connectors work
correctly.
• Gently bend and flex cables, inspecting them for damage or extreme wear, ex-
posed wires, and bent connectors.

Art. no.: 2.540103 Rev.b

• Confirm that all connectors engage securely.
The casing of the CARDIOVIT AT-1 G2 and the cable assemblies can be cleaned with
a cloth slightly moistened (not wet) on the surface only. If necessary, a domestic non-
caustic cleaner or a 50 % alcohol solution can be used to remove grease stains and
finger prints. Wipe the equipment with a cloth slightly moistened (not wet) with one of
the approved cleaning solutions (see section 5.2.2). Thoroughly wipe off any excess
cleaning solution. Do not let the cleaning solution run into or accumulate in connector
openings, switches, or gaps. If liquid gets into connectors, dry the area with warm air
and check that the device operates properly.

Page 24
 Maintenance 5
CARDIOVIT AT-1 G2 Service handbook Cleaning the casing and cables 5.2

5.2.1 Cleaning cable assemblies

1. Before cleaning, inspect the cable for damage. Gently bend and flex all parts of
the cable. Inspect for splits in the sheathing, damage or extreme wear, exposed
wires or bent connectors.
2. Wipe the cable with a cloth slightly moistened (not wet) with one of the approved
cleaning solutions listed below.
3. Gently grip the cable with the damp cloth in the centre of the cable and slide the
cable through the cloth 20 cm at a time until clean. Do not clean the whole length
in one single action as this may cause ‘bunching‘ of the insulation sheathing.

20 cm 20 cm 20 cm 20 cm

4. Thoroughly wipe off any excess cleaning solution. Do not let the cleaning solution
run into or accumulate in connector openings, switches, or gaps. If liquid gets into
connectors, dry the area with warm air.

OK Wrong!
OK

5.2.2 Admissible detergents

• 50 % isopropyl alcohol
• neutral, mild detergent
• all products designed for cleaning plastic.

5.2.3 Non-admissible detergents

Never use products containing the following:
Art. no.: 2.540103 Rev.b

• Ethyl alcohol
• Acetone
• Hexane
• Abrasive cleaning powder
• Plastic-dissolving products

Page 25
5 Maintenance
5.3 Disinfection CARDIOVIT AT-1 G2

5.3 Disinfection
Disinfection removes certain bacteria and viruses. Please refer to the manufacturer's
information. Use commercially available disinfectants intended for clinics, hospitals
and medical practices.

Disinfect the device in the same way as described for cleaning the device (previous
page).

5.3.1 Admissible disinfectants

• Isopropyl alcohol 50 %
• Propanol (35 %)
• Aldehyde (2-4 %)
• Ethanol (50 %)
• all products that are suitable for sensitive surfaces, such as:
– Bacillol® 30 foam/ Bacillol® 30 Tissues
(10% Propanol-1, 15 % Propanol-2, 20 % Ethanol)
– Mikrozid® AF (25 % Ethanol, 35 % 1Propanol-1)

5.3.2 Non-admissible disinfectants

Never use products containing the following:

• Organic solvents
• Ammonia-based detergent
• Abrasive cleaning agents
• 100 % alcohol
• Conductive solution
• Solutions or products containing the following ingredients:
– Acetone
– Quaternary ammonium compound
– Betadine
– Chlorine, wax or wax compound
– Ketone
– Sodium salt

Art. no.: 2.540103 Rev.b

Page 26
 Maintenance 5
CARDIOVIT AT-1 G2 Service handbook Cleaning the print head 5.4

5.4 Cleaning the print head

Over a period of time, the printing ink from the grid on the paper can form a film on the
thermal print head. This can cause the print quality to deteriorate. We recommend
therefore that the print head is cleaned with alcohol every month. This is done as
follows:

1. Open the paper tray and remove the paper. The thermal print head is located di-
rectly above the pressure roller (when the paper tray is closed).
2. With a tissue dampened in alcohol, gently rub the printhead to remove the ink res-
idue. If the print head is badly soiled, the colour of the paper grid ink will show on
the tissue.

5.4.1 Replacing pressure roller print head

Pull out the roller and place a new roller into the position.

 Check the printer after replacement.

Art. no.: 2.540103 Rev.b

Page 27
5 Maintenance
5.5 Battery CARDIOVIT AT-1 G2

5.5 Battery
• The lead gel battery does not require any maintenance.
• Replace the battery approx. every 4 years (depending on the application) when the
battery running time falls substantially under one hour.
• Storage and operation conditions outside the temperature range of 15-25 °C will
reduce the service life of the battery!
• Make sure that the battery remains charged during storage. If the device is not
used for more than 3 to 4 months, the battery needs to be protected from deep dis-
charge by recharging it; the ideal capacity is 50-80%. If a fully charged battery is
stored for a long period of time, this may reduce its service life.

5.5.1 Charging the battery

A totally discharged battery requires approximately 4 hours to be 90% charged (when
the unit is switched off). It is possible to use the unit when the battery is being charged;
however, the charging time may be longer.

No harm will be done to the battery by leaving the unit connected to the mains supply.

1. Connect the device to the mains supply.

2. The blinking battery LED indicates that the battery is being charged.
3. Charge the battery for at least 4 hours.

5.5.2 Battery disposal

The battery must be disposed of in municipally approved areas or sent back to

SCHILLER AG.

 Explosion hazard! The battery must not be burned or disposed of in domestic

waste.
 Danger of acid burns! Do not open the battery.

Art. no.: 2.540103 Rev.b

Page 28
 Maintenance 5
CARDIOVIT AT-1 G2 Service handbook Inspection Report 5.6

5.6 Inspection Report

 The user guide, especially chapter 9.4, must be read before the inspection.
 Recommended inspection interval: Every 6 months

Serial no.: ________________

Test Results Date

Visual inspection 5.1

• Casing not damaged ❒ ❒ ❒ ❒ ❒
 External condition
• Electrode connector port not dam-
aged
❒ ❒ ❒ ❒ ❒
 Availability and condition of ac- • ECG Electrodes (expiration date
cessories and compatibility)
❒ ❒ ❒ ❒ ❒
• User guide ❒ ❒ ❒ ❒ ❒
• Mains and patient cable ❒ ❒ ❒ ❒ ❒
Functional test 3.1 • No error message shown in the
standard display
❒ ❒ ❒ ❒ ❒
 ECG test
 Keyboard test • Keyboard is working ❒ ❒ ❒ ❒ ❒
 Check the battery • Battery OK ❒ ❒ ❒ ❒ ❒
 Printer • Contrast and line strength ❒ ❒ ❒ ❒ ❒
• Cleaning the thermal print head ❒ ❒ ❒ ❒ ❒
Remarks
Art. no.: 2.540103 Rev.b

 Recurrent test conducted (every

12 months)
❒ ❒
Inspection carried out by:

In case of a defect, please contact the service department of your hospital ❒, your
SCHILLER representative ❒ or the local after-sales service ❒.

Name: ...................................................................
Phone: ...................................................................

Page 29
5 Maintenance
5.7 Accessories and disposables CARDIOVIT AT-1 G2

5.6.1 Lifed-item replacement every 3 - 5 years

Inspection Results Replacement
Internal battery
 Replace Internal Accumulator if • Unit sent to SCHILLER service     
operation falls substantially under centre for accumulator replace-
one hour. ment.
Date of replacement:
Inspector:

5.7 Accessories and disposables

 Always use SCHILLER spare parts and disposables or products approved by
SCHILLER. Failure to do so may endanger life and/or invalidate the warranty.

Your local representative stocks all the disposables and accessories available for the
CARDIOVIT AT-1 G2. A comprehensive list of all SCHILLER representatives can be
found on the SCHILLER website (www.schiller.ch). In case of difficulty, contact our
head office. Our staff will be pleased to help process your order or to provide
information on all SCHILLER products.

Art. no.: Article

2.310320 Earth cable for the potential equalisation stud

2.400095 10-wire patient cable, IEC, 3.5 m, push-button

2.400104 10-wire patient cable, AHA, 3.5 m, push-button

2.400070 10-wire patient cable, IEC, 2 m, banana plug

2.400071 10-wire patient cable, AHA, 2 m, banana plug

2.000041 Electrode kit for adults

2.000052 Electrode kit for children

2.155025 Blue Sensor Disposable ECG Electrode

2.155031 Biotabs Ag/AgC electrodes for resting ECG

Art. no.: 2.540103 Rev.b

2.155032 Adapter snap/clip for banana plug cables (10 pieces)

2.157044 Thermal chart paper, Z-folded

2.157045 Thermal chart paper roll

2.300003 Mains cable AC Swiss 90° angled

2.300004 Mains cable UK, 90° angled

2.300005 Mains cable Schuko Europe, 90° angled

2.300014 Mains cable China

2.300016 Mains cable Japan

2.300024 Mains cable USA hospital grade

2.300025 Mains cable Brazil

Page 30
 Trouble Shooting 6
CARDIOVIT AT-1 G2 Service handbook Possible problems 6.1

6 Trouble Shooting
6.1 Possible problems
Error Possible causes and indicators Error localisation and troubleshooting
• No mains supply; mains indica-  Check the mains cable and connection
tor on the device is off.  If the mains indicator is lit, it indicates that power is reaching the
• Battery defective/empty unit and the internal power supply should be OK. Press and hold
the On/Off key for 10 seconds. Wait a few seconds and switch the
device on again.
Unit does not switch
on, blank screen  Check / change the battery. If the battery is faulty, it is possible that
the unit cannot be switched on even if the mains supply is
connected.
 If the screen is still not lit, it indicates a software error, monitor or
internal power supply problem. Call your local SCHILLER
representative.
• Incorrect settings for patient  Change sensitivity setting.
 Check electrode contact and re-apply the electrodes.
QRS traces overlap • Bad electrode contact  If the unit is still not working, call your local SCHILLER representa-
tive.
 NOTE: Some patients have very high amplitudes and even on the
lowest sensitivity settings, the QRS traces can overlap.
• High resistance between skin  Check the electrode resistance (all leads need to be shown in
and electrodes green)
 Re-apply the electrodes.
• Patient not relaxed  Ensure that the patient is relaxed and warm.
• Incorrect settings  Check all filter settings (Menu key > Filter & formulas).
"Noisy" traces  Activate the myogram filter and change the cut-off frequency.
 Ensure mains filter is correct for mains supply.
 If the problem persists, call your local SCHILLER representative.
 Specific devices labelled with the symbol may interfere with
• Electromagnetic interferences the ECG signal. Switch such devices off and/or generally maintain
a sufficient distance to other electric/electronic devices (see chap-
Art. no.: 2.540103 Rev.b

ter 10.2).
• No paper  Ensure that paper is loaded.
• Paper incorrectly loaded  Reload paper.
 Ensure that the paper has been inserted correctly with the black
No printout obtained
mark at the top.
after an auto mode
recording. • Incorrect settings  Check that the printout is activated for at least one setting, and that
Print after acquisition is activated (see page 21)
 If the printer still doesn‘t work, call your local SCHILLER represent-
ative.
• Old paper inserted  Ensure that new SCHILLER paper is inserted.
 Note that the CARDIOVIT AT-1 G2 thermal paper is heat- and light-
sensitive. If it is not stored in its original seal, stored in high temper-
Printout fades, is not atures or is simply old, print quality can deteriorate.
clear, or the printout
 Over a period of time, the printing ink from the grid on the paper can
is ‘patchy‘ • Dirty print head form a film on the thermal print head. Clean the thermal print head.
• Print-head out of adjustment  If the printer still doesn‘t work, call your local SCHILLER represent-
ative.

Page 31
6 Trouble Shooting
6.1 Possible problems CARDIOVIT AT-1 G2

Error Possible causes and indicators Error localisation and troubleshooting

No printout of • Incorrect settings
interpretation
 Check that the interpretation and measurement options are ena-
statement,
bled for the printout. (See page 21 sections 4.2.4 and 4.2.5.)
averaged cycles or
measurements
• Software hangs up  Switch off and on again after a few seconds.
 Press and hold the On/Off button for 10 seconds to force the device
Keyboard blocked to switch off. Reconnect mains and switch on.
 If the unit is still not working, call your local SCHILLER representa-
tive.

Art. no.: 2.540103 Rev.b

Page 32
 Trouble Shooting 6
CARDIOVIT AT-1 G2 Service handbook Preventing electromagnetic interferences 10.2

10.2 Preventing electromagnetic interferences

The user can help avoid electromagnetic disturbances by keeping the minimum
distance between portable and mobile HF telecommunication devices (transmitters)
and the CARDIOVIT AT-1 G2. The distance depends on the output performance of
the communication device as indicated below.
“Non ionising electromagnetic radiation"

Transmitter fre- Testing fre- Max.

HF source Distance d
quency quency power P
Wireless communications devices [m]
[MHz] [MHz] [W]

385
Various radio services (TETRA 400) 380-390 1.8 0.3

- Walkie-talkies (FRS)
430-470 450 2 0.3
- Rescue service, police, fire brigade, servicing (GMRS)
LTE band 13/17 704-707 710/745/780 0.2 0.3
- GSM800/900
- LTE band 5 800-960 810/870/930 2 0.3
- Radio telephone (microcellular) CT1+, CT2, CT3
- GSM1800/1900
- DECT (radio telephone) 1720/1845/
1700-1990 2 0.3
- LTE Band 1/3/4/25 1970
- UMTS
- Bluetooth, WLAN 802.11b/g/n
- LTE Band 7
2400-2570 2450 2 0.3
- RFID 2450 (active and passive transponders and
reading devices)
5240/5500/
WLAN 802.11a/n 5100-5800 0.2 0.3
5785

 Portable HF telecommunication devices must not be used within a radius of

0.3 m from the CARDIOVIT AT-1 G2 and its cables.
 Do not place the CARDIOVIT AT-1 G2 on top of other electric/electronic devices
- i.e. maintain a sufficient distance to other devices (this includes the patient
cables).
Art. no.: 2.540103 Rev.b

For permanent HF telecommunication devices (e.g. radio and TV), the recommended
distance can be calculated using the following formula: d = 0.6  P . (The formula
is based on the max. immunity level of 10 V/m in the frequency domain of 80 MHz to
3000 MHz).

d = recommended minimum distance in meters

P = transmitting power in Watts

For more information on operation in an electromagnetic environment according to

IEC/EN 60601-1-2, please consult the service manual.

Page 33
6 Trouble Shooting
10.2 Preventing electromagnetic interferences CARDIOVIT AT-1 G2

10.2.1 Measures to prevent electromagnetic interferences

The user can take the following measures to prevent electromagnetic interferences:
• Increase distance to the source of interference.
• Turn the device to change the angle of radiation.
• Connect the potential equalisation cable.
• Connect the device to a different mains connector.
• Only use original accessories (especially patient cables).
• Immediately replace defective cables, especially patient cables with defective
sheathing.
• Make sure the patient cable is securely screwed on.
• Observe the maintenance intervals as stated in Section 5 Maintenance, page 23.

Art. no.: 2.540103 Rev.b

Page 34
 Software update& Licence key upgrade 7
CARDIOVIT AT-1 G2 Service handbook Software update procedure 7.1

7 Software update& Licence

key upgrade
• USB memory stick
• Download the software from Schiller extranet.
• Copy the ATN1 folder to the root folder of a USB Stick.
• This ATN1 folder must contain the correct Firmware and Bootloader (ATN1f-
wv_Vxxx.bin and ATN1btldv_Vxxx.bin).

7.1 Software update procedure

1. Connect the device to mains supply
2. Plug in the USB stick with the software (Folder ATN1 with software
ATN1fwv_Vxxxx.bin and ATN1btldv_Vxxx.bin)
3. Switch the device on. The Software update dialog appears
4. Confirm the dialogue with the Menu/Enter key.
Software update
New Version
BL V 1.0.xxx
FW V 1.0.xxx
Do you want to update now?

YES NO

5. Progress bar is displayed.

6. After Successfully installed software, remove the USB stick to initialise the re-
booting of the device
7. Execute a functional tests according to the instructions (see page 29, 5.6 Inspec-
tion Report)

7.2 Licence key upgrade procedure

Art. no.: 2.540103 Rev.b

• USB memory stick

• Copy the licence file (serial number.lic) to USB memory stick into the root folder.
1. Connect the device to mains supply
2. Plug in the USB stick with the licence key.
3. Switch the device on.

4. Go to Menu/Information and press the button Manual print .

5. Confirm the dialogue with the Menu/Enter key.

Software upgrade Software upgrade Software upgrade

Do you want to upgrade? Do you want to upgrade? Do you want to upgrade?

<Standard> <Interpretation> <Interpretation, CCAA>

YES NO YES NO YES NO

6. Progress bar is displayed.

7. After Successfully installed licence, remove the USB stick to initialise the reboot-
ing of the device.

Page 35
7 Software update& Licence key upgrade
7.2 Licence key upgrade procedure CARDIOVIT AT-1 G2

8. Go to Menu/Information and check the SW options.

Art. no.: 2.540103 Rev.b

Page 36
 Unit test and configuration 8
CARDIOVIT AT-1 G2 Service handbook Basic unit test 8.1

8 Unit test and configuration

The basic unit test is a production test. The new unit will always start in the basic unit
test mode when the main board is new.

8.1 Basic unit test

• ECG simulator
• Print paper

• This test can be initialised also with Go to Menu/Information and type 3 9 2

• Exiting the test is possible with 391
• If battery test is not needed skip this test with key sequence 938
The following procedure is given:
1. Check for software update (press twice enter and then the arrow key down to skip
this check)
2. Check keyboard (press every key, except the on/off)
3. Set time
4. Set date
5. S/N input (enter the same S/N number as printed on the device)
6. Start ECG printout (connected ECG simulator required)
7. Confirm that ECG printout (Test PASSED is OK with the Menu/enter key. The de-
vice is switch off). Switch the device on again. The unit will continue with step 8.
8. Battery test. After switching on the Check battery condition test is initialised. Fol-
lowing the procedure. This can take several hours. When this test is finalized the
date and running time is displayed
9. Start SW update check.
10. Exit to Storage or to configure 
• Storage is selected when the device goes back to storage an no further customized
configuration is need. If taking “storage” devices follow procedure page 38, 8.2
Configuration & End test after storage.
• Configure (& End Test) is used to:
– enter license code (via USB)
Art. no.: 2.540103 Rev.b

– Executing CTS test with the CAL 2016

– Transfer report with to USB (xml)
see details page 38, 8.2 Configuration & End test)

Page 37
8 Unit test and configuration
8.1 Basic unit test CARDIOVIT AT-1 G2

Basic unit test 28.08.2016 17.58

SW update (1) check for SW update Check Battery cond (8) run charge/discharge

Check keyboard (2) Press every key SW Update (9) 1.0.2.R2

Set Date (3) 21.03.2017 Exit (10) Storage mode or Configuration 

Set time (4) 8:01

S/N input (5) 1070.00016

ECG Test Printout (6) start ECG printout

Exit (7) Test in Progress Test PASSED

Art. no.: 2.540103 Rev.b

Page 38
 Unit test and configuration 8
CARDIOVIT AT-1 G2 Service handbook Configuration & End test 8.2

8.2 Configuration & End test

• ECG simulator with CAL2016

The Configuration and End test will call up at the end Step 10 of the basic unit, when
“Configuration” is selected.

1. Plug in the USB memory stick with the license key

2. Start ECG printout (connected ECG simulator with the CAL 2016 required)
3. Write the report to the USB memory Stick (inkl. Test results of the ECG in xml
format)
4. Exit configuration. The device is now ready for use.

Config & End Test 28.08.2016 17.58

SW License(1) load license (USB)

CTS Test (2) ECG signal CAL2016

Transfer report (3) write report (USB)

Exit (4) Configuration or Storage 

execute

8.2.1 Configuration & End test after storage

Art. no.: 2.540103 Rev.b

This procedure will be only used for device from stock. This device have been tested
according basic unit test, but do not have a customized licence key and a ECG
performance test.

• Do not use this procedure to update only licence key. For this procedure see
page 35, 7.2 Licence key upgrade procedure.

 Go to Menu/Information and type 3 9 8 Config & End Test. The same test as in
chapter 8.2 appears.

Page 39
9 Technical Data
9.1 Device CARDIOVIT AT-1 G2

9 Technical Data
9.1 Device
Dimensions 285 x 189 x 61 mm, approx. 1.94 kg incl. thermal paper

Display • Colour LCD

• Resolution: 800 x 480 dots, 5 “
Power supply 100 - 240 VAC, max. 0.75 A(115 V) - 0.4 A(230 V), 50/60 Hz
Mains-independent operation with built-in rechargeable battery

Power consumption max. 30 W

Battery
Capacity • Pb gel battery 12 V, 2.0 Ah
• 4 hours normal use without printing
Battery life Under normal operating conditions, 4 years
Recharging time 90%: approx. 4 hours when the device is switched off
Printer High-resolution thermal head printer; 8 dots/mm (amplitude axis); 20 dots/mm (time
axis) @ 25 mm/s
Frequency range Complies with IEC 60601-2-25 and ANSI/AAMI EC11
Chart paper Thermo-reactive, Z-folded, 80 mm wide
Thermo-reactive, roll, 80 mm wide
Speed • 5 / 25 / 50 mm/s (for resting ECG: 25 / 50 mm/s)
Sensitivity • 5 /10 / 20 mm/mV (for resting ECG: 10 mm/mV)

ECG display ECG is displayed on an area of 108 x 65 mm

Speed • 5/ 25/ 50 mm/s
Sensitivity • 5 /10 / 20 mm/mV
Interfaces • ECG cable interface
• Potential equalisation

Art. no.: 2.540103 Rev.b

• 1 USB
Internal memory • 100 ECG’s in PDF format (only for export to USB memory stick)

Ambient conditions
Operating temperature • 10 to 40 °C
Relative humidity • 20 to 90% (non-condensing)
Pressure during operation • 780 to 1060 hPa

Storage temperature • 5 to 50 °C
Transport temperature • -10 to 50 °C
Humidity during storage/transport • 10 to 95% (non-condensing)
Pressure during storage/transport • 500 to 1060 hPa

Page 40
 Technical Data 9
CARDIOVIT AT-1 G2 Service handbook Device 9.1

Environmental conditions EMC • IEC/EN 60601-1-2

• CISPR 11/32 Group 1, class B
The CARDIOVIT AT-1 G2 can be exposed to the following interferences without any
impairment of the essential performance features:

• static discharge up to ±8 kV contact, ±15 kV air

• radio frequency range up to 10 V/m (80 to 3000 MHz)
• near fields of wireless HF telecommunication devices 9 to 28 V/m (385-
5785 MHz), for more details, see table on page 44.
• magnetic fields of 30 A/m, 50 Hz
Art. no.: 2.540103 Rev.b

Page 41
9 Technical Data
9.2 ECG CARDIOVIT AT-1 G2

9.2 ECG
Patient input Fully floating and isolated, defibrillation-protected (only with original SCHILLER pa-
tient cable)

Lead configurations • Standard 12 channels

Display
Leads • Display of selected leads (3 x4)
• Filter status
• Power source
Status
• Leads
• Electrode contact status
• Heart rate (HR)
• Date and time
• Patient ID

Filter
Myogram filter (muscle tremor) Set to 25, 40, 150, 250 Hz (250 Hz = Filter Off)
Notch filter Distortion-free suppression of superimposed AC 50 or AC 60 Hz sinusoidal interfer-
ences by means of adaptive digital filtering
Data record • Listing of all ECG recording data (date, time, filter)
• ECG measurements results (intervals, amplitudes, electrical axes)
With optional interpretation ETM • Averaged complexes
• Guidance on interpreting adult and paediatric ECGs
ECG amplifier Complies with IEC 60601-2-25 and ANSI/AAMI EC11

9.3 Safety Standards

Safety standard IEC/EN 60601-1
IEC/EN 60601-2-25

Art. no.: 2.540103 Rev.b

EMC IEC/EN 60601-1-2

Protection class Device as a system: Class I according to IEC/EN 60601-1

Conformity/classification CE/IIa in accordance with directive 93/42/EEC

Protection This device is not designed for outdoor use (IP 20)

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 Technical Data 9
CARDIOVIT AT-1 G2 Service handbook EMC information 9.4

9.4 EMC information

The unit meets the Collateral Standards of Electromagnetic compatibility – Require-
ments and tests IEC/EN 60601-1-2 the limits and methods of measurement of elec-
tromagnetic disturbance characteristics of industrial, scientific and medical radio fre-
quency equipment.

Medical electrical equipment is subject in regard to the electromagnetic compatibility

(EMC) and its special precautionary measure.

The unit must in reference to the mentioned EMC-hints in the accompanying docu-
ments be installed and operated.

This medical device is intended for use in the electromagnetic environment specified
in the following tables. The user of this device should ensure that it is used in such an
environment.

9.4.1 Electromagnetic emissions

Emission
RF emissions CISPR 11/32
RF emissions CISPR 11
Harmonic emissions IEC 61000-3-2
Voltage fluctuations/Flicker emissions
IEC 6100-3-3
Test Compliance Electromagnetic environment guidance
This device uses RF energy only for its internal function. Therefore
Group 1 its RF emission are very low and are not likely to cause any interfer-
ence in nearby electronic equipment.
Class B
The device is suitable for use in all establishments, including those
Class A
directly connected to the public low-voltage power supply network
that supplies buildings used for domestic purposes.
Complies

9.4.2 Immunity
Immunity Test IEC 606101 Test level Compliance Level Electromagnetic environment guidance
Floors should be wood, concrete or ceramic tile. If
ESD ±8kV Contact ±8kV Contact
floors are synthetic, the relative humidity (RH)
IEC 61000-4-2 ±15kV Air ±15kV Air
should be at least 30%.
EFT ±2kV Power supply lines ±2kV Power supply lines Mains power quality should be that of a typical
IEC 61000-4-4 ±1kV I/O lines ±1kV I/O lines commercial or hospital environment.
Surge ±1kV differential mode ±1kV differential mode Mains power quality should be that of a typical
IEC 61000-4-5 ±2kV common mode ±2kV common mode commercial or hospital environment.
Art. no.: 2.540103 Rev.b

< 5% UT < 5% UT
(> 95% dip in UT) (> 95% dip in UT)
for 0,5 cycle for 0,5 cycle

40% UT 40% UT
(60% dip in UT) (60% dip in UT)
for 5 cycles for 5 cycles Mains power quality should be that of a typical
Voltage Dips/Dropout
commercial or hospital environment. The unit
IEC 61000-4-11
70% UT 70% UT shutoff during the >95% for 5 second disturbance.
(30% dip in UT) (30% dip in UT)
for 25 cycles for 25 cycles

< 5% UT < 5% UT
(> 95% dip in UT) (> 95% dip in UT)
for 5 s for 5 s
Power Frequency 50/60Hz
Power frequency magnetic fields should be that of
Magnetic Field 30 A/m 30 A/m
a typical commercial or hospital environment.
IEC 61000-4-8
NOTE UT is the AC mains voltage prior to application of the test level.

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9 Technical Data
9.4 EMC information CARDIOVIT AT-1 G2

9.4.3 Emissions equipment and systems

Immunity Test IEC 606101 Test Level Compliance Level Electromagnetic environment guidance
Portable and mobile communications equipment
should be used no closer to any part of this
device, including cable, than the recommended
separation distance (d) calculated from the equa-
tion applicable to the frequency of the transmitter

Recommended separation distance:

3 Vrms outside ISM band
Conducted RF 6 Vrms in the ISM & amateur
[V1] = 10 Vrms 3.5
IEC 61000-4-6 radio band d = --------  P
150 kHz to 80 MHz V1

Radiated RF 10 V/m [E1] = 10 V/m

6
IEC 61000-4-3 80 MHz to 2700 MHz 80 MHz to 3000 MHz d = ------  P for 80 MHz to 3000 MHz
E1

see Section 9.4.4 Immunity to Section 9.4.4 Immunity to 6

Proximity fields from RF d = ------  P for tested frequencies
proximity fields from RF wire- proximity fields from RF wire- E1
wireless communications
less communications equip- less communications equip-
equipment IEC 61000-4-3 Tested Frequency see Section 9.4.4 Immunity to
ment, page 44 ment, page 44
proximity fields from RF wireless communications
equipment, page 44
where P is the maximum power in watts and d is
the recommended separation distance in meters.

Field strengths from fixed transmitters, as deter-

mined by an electromagnetic sitea survey, should
be less than the complianceb levels (V1 and E1).

Interference may occur in the vicinity of equip-

ment marked with following Symbol

“non ionizing radiation”

Art. no.: 2.540103 Rev.b

Note 1 At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,
AM and FM radio broadcast ant TV broadcast cannot be predicted theoretically with accuracy. To access the electromagnetic environment
due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which
the device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocation the device.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.

Page 44
 Technical Data 9
CARDIOVIT AT-1 G2 Service handbook EMC information 9.4

9.4.4 Immunity to proximity fields from RF wireless communications

equipment
Test max.
frequency Banda Service
Modulation
power P
Abstand d Immunity
[MHz] [m] level [V/m]
[MHz] [W]

Pulse
Various radio services (TETRA
385 380-390
400) modulationb 1.8 0.3 27
18 Hz

- Walkie-talkies (FRS) FM c
450 430-470 - Rescue service, police, fire bri- ±5 KHz 2 0.3 28
gade, servicing (GMRS) ±1 KHz sine
710 Pulse
745 704-707 LTE band 13/17 modulation 0.2 0.3 9
780 217 Hz
- GSM800/900
810 Pulse
- LTE band 5
870 800-960 modulation 2 0.3 28
- Radio telephone (microcellular)
930 18 Hz
CT1+, CT2, CT3
- GSM1800/1900
1720 Pulse
- DECT (radio telephone)
1845 1700-1990 modulation 2 0.3 28
- LTE Band 1/3/4/25
1970 217 Hz
- UMTS
- Bluetooth, WLAN 802.11b/g/n
- LTE Band 7 Pulse
2450 2400-2570 - RFID 2450 (active and passive modulation 2 0.3 28
transponders and reading devic- 217 Hz
es)
5240 Pulse
5500 5100-5800 WLAN 802.11a/n modulation 0.2 0.3 9
5785 217 Hz

a.For some services, only the uplink frequencies are included.

b.The carrier shall be modulated using a 50 % duty cycle square wave signal.
c.As an alternative to FM modulation, 50 % pulse modulation at 18 Hz may be used because while it does not
represent actual modulation, it would be worst case
Art. no.: 2.540103 Rev.b

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9 Technical Data
9.4 EMC information CARDIOVIT AT-1 G2

9.4.5 Recommended separation distances

For fixed installed HF-Transmitters (z.B Radio und TV transmitters) the following minimum dis-
tance to the transmitter can be calculated as follows:.

Maximum Power
Separation distance according frequency of the transmitter
Output [m]
[Watts]
150 kHz to 80 MHz 80 MHz to 3000 GHz
3.5 6
d = --------  P d = ------  P
V1 E1

0.01 0.04 0.06

0.1 0.11 0.19
1 0.35 0.6
10 1.1 1.9
100 3.5 6
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts [W] according
to the transmitter manufacturer.

Note 1 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,
objects and people.

Art. no.: 2.540103 Rev.b

Page 46
 Opening housing 10
CARDIOVIT AT-1 G2 Service handbook Disassembly AT-1 G2 10.1

10 Opening housing
10.1 Disassembly AT-1 G2
Opening the CARDIOVIT AT-1 G2 housing is needed for replacing and repairing of
Battery, LCD, PCB and Printer

• size 1 Philips screw driver

1. Close the printer cover before loosen the screw!

2. Protect LCD from scratches with a LCD protection plastic foil.

Fig. 10.1 AT-1 G2 bottom view

Do not try to lift up the top part with the LCD. Proceed as shown on the picture below.

3. Lift up the bottom housing as shown and disconnect the battery supply.
Art. no.: 2.540103 Rev.b

Fig. 10.2 Lift up bottom housing

Page 47
10 Opening housing
10.1 Disassembly AT-1 G2 CARDIOVIT AT-1 G2

10.1.1 Replacing battery

 Pull out both brackets. Now you can lift up the battery and pull it out of the bottom
bracket.

10.1.2 Reassembly
The following is just a brief procedure description for reassembly

1. Add the two adhesive tapes.

2. Put the battery in place.
3. Connect the battery cables and pace the cable as shown below

4. Connect the battery cable to the main board.

Art. no.: 2.540103 Rev.b

5. Close the housing and tighten all 8 screws.

Fig. 10.3 Reassembly

Page 48
 Index 11
CARDIOVIT AT-1 G2 Service handbook

11 Index
A
Accessories and disposables 39, 45
Address Headquarters ......................... 2

B
Battery
Battery life ........................................ 39
Capacity ........................................... 39
Recharging time .............................. 39
Battery operation ................................ 15

C
Cleaning ............................................... 24

I
Isolating from the mains .................... 16

K
Keys ...................................................... 11

M
Maintenance ............................. 23, 42

P
Potential equalisation ......................... 14
Power supply ....................................... 15

S
Safety Notes .......................................... 5
Sequential ............................................ 20
Simultaneous ...................................... 20
Switching On / Off .............................. 15
Art. no.: 2.540103 Rev.b

Page 49
11 Index
CARDIOVIT AT-1 G2

Art. no.: 2.540103 Rev.b

Page 50