-
Operating Manual
Resting and Stress ECG
Part 2: Hardware, description of device for custo cardio 400
BT
1 2 3 4Safety Hardware Software Hygiene
Operating characteristics:12-channel PC ECG,Resting & stress
ECG
MHW 0012 – DK 1713Version 003 – 06/08/2019
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© 2019 custo med GmbHThis Operating Manual may not be copied in
its entirety or in part, duplicated in any form or by any means or
translated into another language without the prior written consent
of custo med GmbH.
The manufacturer reserves the right to change the information in
this Operating Manual without prior notice. The current version can
be downloaded from our web-site: www.customed.de.
CAUTION: This Operating Manual is part of a modular system,
consisting of four parts. All four parts must be downloaded from
the Internet or from a CD to ensure the Operating Manual is
complete.
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Table of contents
2.1 Symbols on the devices . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . .42.2 Intended use . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . .52.3 Part names, components for the
recording . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . .62.4 Assembly and device operation
2.4.1 Setting the telescope boom and mounting it on the device
trolley . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
.7 2.4.2 Placing the device in the telescope boom . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . .8 2.4.3
Preparing patient leads . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . .9 2.4.4 custo cardio 400 BT – device operation . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102.5
Examination procedure . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . .122.6 Attaching the device to the patient
2.6.1 Electrode application . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . .13 2.6.2 Instructions for the stress ECG with
treadmill . . . . . . . . . . . . . . . . . . . . . . . . . . .
.142.7 Technical data and system requirements . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
.152.8 Manufacturer's declaration regarding EMC. . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
.82.9 EC Declaration of Conformity . . . . . . . . . . . . . . . .
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . 212.10 List of product components and
accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . .
. . . . . . . . . . . . .23
Operating Manual
Resting and Stress ECG
Part 2: Hardware, description of device for custo cardio 400
BT
1 2 3 4Safety Hardware Software Hygiene
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GmbH
2Resting and Stress ECGHardware, description of device for custo
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2.1 Symbols on the devices
Manufacturer: custo med GmbH, Maria-Merian-Str. 6, 85521
Ottobrunn, Germany Production date (YYYY-MM, e.g. 2018-01)
CE mark, notified body
Observe the Operating Manual
Medical electrical equipment classificationaccording to DIN EN
60601-1 (Type CF)
Non-ionising electromagnetic radiation, Device contains a RF
transmitter
Separate collection of electrical and electronic equipment,do
not dispose with domestic waste
Hygiene seal of the German Society of Hospital Hygiene
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2.2 Intended use
custo cardio 400 BT is a 12-channel electrocardiograph with an
integrated electrode application system which is used in
professional applications as a resting or stress ECG. The electrode
application system uses underpressure to attach the electrodes to
the body of the patient. The intercardial application is not
intended. The terminal lines are R, L and F according to Einthoven
and C1 to C6 according to Wilson.
custo cardio 400 BT is perfectly safe for patients with a
pacemaker. The ECG record-ing is not affected by pacemaker
pulses.
The device must be operated by suitably trained and qualified
personnel in medical practices, laboratories, rehab centres and
hospitals. In particular, these include doctors and
medical-technical personnel. The intended use of this device does
not include use in home settings, especially by laypersons.
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C3
C2
C1
R
N
max
min
C3
C2
C1
R
N
max
min
2.3 Part names, components for the recording
custo cardio 400 BT with Bluetooth & USB custo cardio 400 BT
ECG application system 6 thoracic wall leads (1.20 m) and
4 extremity leads (1.45 m) Electrode “hair”, other versions
optional Spacer 2-fold Spacer 3-fold Telescopic boom for custo
cardio 400 BT Bracket for telescopic boom Cable hook for electrode
leads (not pictured) Bluetooth-USB adapter (Bluetooth 4.0) USB
extension cable BT power supply unit for custo cardio 400 BT 1.5 m
power cable for power supply unit 3 m USB cable
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2.4 Assembly and device operation
2.4.1 Setting the telescope boom and mounting it on the device
trolley
Anti-turn device for fixing the boom, in the open position
during operation (270° swivel range)
Continuous height adjustment with gas pressure spring Gas
pressure spring Extraction lock to extend and pull in the boom arm
Bracket for custo cardio 400 BT with safety bar
Put the clamps and in position and secure them with an Allen key
(size 5 mm).Mount the clamps straight (aligned) to keep the gas
pressure spring fromjamming.
Use the screw set to fix the bracket to the device trolley ,
place the boomand protective plastic ring in the bracket, set the
swivel range of the boom and then fasten the boom in the bracket
.
400 mm
160 mm
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Push custo cardio 400 BT into the bracket on the boom. To do
this, pull the safety bar back and push the device into the bracket
until it clicks into place so that the safety bar is moved back to
the front.
Operating the telescope boom safelyFollow the instructions below
to safely move the device trolley with the telescopic boom:
Fasten the telescope boom: Tighten the anti-turn device .
Set the angle of the boom arm to 90 degrees: Height adjustment :
Press the lever and simultaneously move the boom arm into the
desired position by moving the end of the boom arm up or down. To
NOT pull the device.
Pull the boom arm in completely: extraction lock .
Assembling custo cardio 400 BTAttach the USB cable to the
device, pull the arm of the boom out until it reaches the maximum
length. Route the USB cable along the boom and fix it using the
Velcro fasteners. Important: Only connect the USB cable after the
installation of the software to the PC.
custo cardio 400 BT Power supply linefor connection to the power
supply unit 1)
1) Note on the power supply: Use only the power supply unit
delivered with the device(item number 85037).
2.4.2 Placing the device in the telescope boom
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Attach the coding labels to the ends of the patient leads.
The labels “C1 to C6” are glued to the chest wall leads (length:
1.20 m) .
The labels “R, L, F and N” are glued to the longer extremity
leads (length: 1.45 m).
Connect the patient leads according to the coding on the device
.
Press the electrodes onto the ends of the electrode leads, until
you hear a click .
C3 C2 C1 R
2.4.3 Preparing patient leads
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On/off button to manually start operations, otherwise automatic
software contro
Status display Suction level control
Controls how strongly the electrodes are fixed to the skin of
the patient (levels 1 to 6 can be set)
Cleaning button – for manually blowing out the leads. This is
otherwise performed automatically by the software.
Prerequisites for the use of the device:Proper installation,
configuration and commissioning of the system.
Examples of visual feedback from the device during operation
Standby mode:The on/off button illuminates in blue
Status after calling up the ECG interface in custo diagnostic
(or in manual mode by pressing the on/off button):The on/off button
and suction level control are illuminated in blue, the status
display shows the preset suction level in the colour of the
connection type, blue for Bluetooth in this case. The suction level
can be adjusted manually by pressing the suction level control
button .
Status after ending the ECG recording, when the ECG interface is
closed:When ending the ECG recording, the electrodes are released
and the leads are blown out. The on/off but-ton and the cleaning
button illuminate in blue, and the status display illuminates green
for the duration of the blow-out. The green status display becomes
smaller according to the progression of the blow-out time (if the
entire duration of the blow-out time is less than one minute).
2.4.4 custo cardio 400 BT – device operation
Status display states:
Turquoise LED = USB modeBlue LED = Bluetooth/WLAN modeOrange LED
= Manual recordingGreen LED = Blow out of the leadsYellow LED =
Warning notification
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Recording functions and procedures: Changing the connection
type
If a USB connection is available, it is prioritised over the
wireless connection because of the higher data rate. The connection
can only be changed by the device (e.g. from Bluetooth to USB) if a
recording is not currently underway.
Manual starting and ending An ECG recording can also be started
by pressing the on/off button instead of using the software
interface. To do this, open the ECG interface in custo diagnostic
and press the on/off button on the device. The status display
illuminates in orange, and the ECG recording proceeds according to
the custo diagnostic configu-ration. Recordings without a time
limit must be ended by pressing the on/off button again (e.g.
rhythm strips).
Automatic suction level controlTo use this function, the suction
level must be set to at least level 3 in custo diagnostic. With
automatic suction power control, the suction level is increased
until the system is airtight and the electrodes rest tightly enough
against the skin of the patient. If the suction level is set
manually, automatic suction level control is deactivated.
Cleaning the electrode leadsThe cleaning function should be used
regularly, e.g. always at the end of a working day. By pressing the
cleaning button, the moisture is blown out of the elec-trode leads
for a longer period of time. Procedure ac-cording to settings in
custo diagnostic, factory setting: 30 minutes. After the cleaning
time has elapsed, the device switches to standby mode.
Device warningsIf there is a technical problem, the status
display illuminates in yellow. Contact your authorised custo med
dealer.
Resetting the Bluetooth connectionAt commissioning or if the
device is deployed in mobile applications, the existing Bluetooth
connection may need to be reset (e.g. to allow the device to
connect to a different work station). To do this press the “+”
and
“-” buttons simultaneously for approx. 2 seconds. The device
turns off briefly.
Figure: USB connection, status display changes from blue
(wireless connection) to turquoise (USB connection)
Figure: Starting a recording manually, status display orange
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2.5 Examination procedure
Prerequisites for an examination:Proper installation,
configuration and commissioning of the system.
Resting ECG Make sure that the ECG device is connected to the
PC
and the power supply of the device is guaranteed. Check that
your patient is lying comfortably and is not cold. Start custo
diagnostic and click:
Examination, Resting ECG, New Resting ECG see Software
description... . Spray the contact spray1) on the electrode
application points. Place the electrodes on the patient according
to the placement diagram,
See 2.6.1 Electrode application. Start the recording. The
patient must keep still during the recording process.
Stress test ECG Make sure that the ECG device is connected to
the PC
and the power supply of the device is guaranteed. When using an
ergometer, make sure that the patient is in the optimal
seating position (the extended leg should be slightly bent).
When using a treadmill, make sure to follow the instructions
in 2.6.2 Instructions for stress ECG with treadmill. Start custo
diagnostic and click:
Examination, Stress ECG, New Stress ECG see Software
description... . Spray the contact spray 1) on the electrode
application points. Place the electrodes on the patient according
to the placement diagram,
See 2.6.1 Electrode application. Wait a few minutes so that the
contact between the skin
and the electrodes can develop optimally. Apply the blood
pressure cuff. Start the recording.
1) Contact spray warningBefore each examination, make sure to
spray contact spray on the electrode application points. Never
spray the contact spray onto the electrodes or into the electrodes
or leads. Do not use water or contact gel!
Recommended contact sprays from: C+V Pharma Depot GmbH or GE
Medical Systems
Only use recommended contact sprays. Residues from other
products can damage the custo cardio 400 BT electrodes.
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2.6 Attaching the device to the patient
2.6.1 Electrode application
Thoracic wall resting and stress ECG, standard according to
WilsonV1 (C1) red 4. Intercostal space at the right sternal
borderV2 (C2) yellow 4. Intercostal space at the left sternal
borderV3 (C3) green on left-hand side of the 5th rib between C2 and
C4V4 (C4) brown 5th intercostal space on the left midclavicular
lineV5 (C5) black on the left-hand side of the anterior axillary
line, at the same height as C4V6 (C6) purple on the left-hand side
of the midaxillary line, at the same height as C4
Extremities resting ECGR red right armL yellow left armF green
left legN black right leg
Stress ECG (lying or standing): extremitiesR red on the right
below the collarboneL yellow on the left below the collarboneF
green on the left above the hipN black on the right above the
hip
Stress ECG (sitting position): extremitiesR red attach to the
deltoid muscle on the rightL yellow attach to the deltoid muscle on
the leftF green 9. Left ribN black 9. Right rib
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2.6.2 Instructions for stress ECG with treadmill
The patient should ideally be wearing running shoes or trainers.
The patient should not hold onto the handles of the treadmill
during
the recording process. This will lead to muscle tension which
will affect the ECG signal.
Missing skin tension, in interaction with shoulder movement,
will increase artefacts in the ECG signal.
The extremity leads should if possible be applied on taut skin
areas in order to avoid excessive movement artefacts and therefore
interference in the other terminal lines.
During the ECG recording, the electrode leads must not come into
contact with the patient, the treadmill or other objects.
Normal electrode application
Artefact reduced electrode application Artefact reduced
electrode application results in smaller amplitudes in the
extremity leads.
Safe use of treadmills with stress ECGAlways set the treadmill
so that the patient can safely move on the device. Ensure that the
acceleration, speed and inclination of the treadmill are adjusted
to the patient's physical constitution, stamina and skill. Observe
the manufacturer's safety instructions.Always inform the patient
before you change the acceleration, speed or inclination.
Otherwise, the patient may become injured, e.g. also due to an
unexpected, abrupt stopping or starting of the treadmill.
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2.7 Technical data and system requirements
custo cardio 400 BT
Number of ECG channels 12
Frequency response 0 to 0.262 * sampling frequency [HZ]
Sampling frequency 1000, 2000, 4000, 8000, 16000 (only with
USB), 32000 (only with USB) Hz
Sampling rate Identical for all channels, possible settings:
1.0 ms / 0.5 ms / 0.25 ms / 0.125 ms / 0.0625 ms (only with USB)
/ 0.03125 ms (only with USB)
Deviation < 1.5 %
A/D converter 24 bit
Input impedance > 50 MΩ
Amplitude quantification 1.526 µV/bit
CMRR > 93 dB
Impedance measurement 1) at all electrode leads (not N) with
automatic quality indication
Defibrillation protection Electrical strength 5000 V
Recovery time after defibrillation < 5 s
Suction power Level 0 = 0 mbar Level 4 = 180 mbar
Level 1 = 60 mbar Level 5 = 220 mbar
Level 2 = 100 mbar Level 6 = 280 mbar
Level 3 = 140 mbar
Power supply 12 V power supply unit
Maximum power consumption 7 Watt
EDV connection USB (3 m) and Bluetooth 2.1 EDR
Radio frequency band Bluetooth 2.1 EDR: 2.402 – 2.480 GHz (ISM
Band)
Radio transmitting power Bluetooth 2.1 EDR: max. 10 dBm
Bluetooth range generally 10 m, depending on ambient
conditions
Time to standby mode2) after disconnection from USB 30 min
last BT communication 30 min
last manual configuration 30 min
IP protection class IPX0 (not protected from water
permeation)
Dimensions 250 * 110 * 60 mm (L * W * H)
Weight approx. 680 g (device without leads and electrodes)
Patient leads approx. 1450 mm (extremities)
approx. 1200 mm (chest wall)
Operating conditions Temperature +10°C ... +40°C
Air humidity 30 ... 75 % rH
Air pressure 700 ... 1060 hPa
Transport and Temperature -20°C ... +45°C
Storage conditions Air humidity 10 ... 95% rH
Air pressure 700 ... 1060 hPa
Classification Device with external power supply,
Class IIa according to MDD, Type CF application part
Underlying standards DIN EN 60601-1, DIN IEC 60601-2-25; DIN EN
60601-1-2
1) Does not apply to Bluetooth devices.2) The pump and value are
deactivated in standby mode. Communication via USB/BT as well as
manual configuration of the system are still possible. Standby mode
is not activated during an ECG recording.
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General system requirements
Operating system Windows 7 SP1 – with current updates
(32 bit and 64 bit operating system)
Windows 8 (32 bit and 64 bit operating system)
Windows 8.1 (32 bit and 64 bit operating system)
Windows 10 (32 bit and 64 bit operating system)
Windows Server 2003 (32 bit and 64 bit operating system)
Windows Server 2008 (32 bit and 64 bit operating system)
Windows Server 2008 R2
Windows Server 2012
Windows Server 2012 R
older versions are not supported
PC The PC hardware should meet the minimum requirements of
the
operating system used. Provide additional RAM (1 GB) for
custo diagnostic. Please ensure that there is sufficient free
space
on the hard disk for the custo diagnostic evaluations.
The PC must meet the requirements of the safety standard
DIN EN 60950 for information technology equipment.
File sizes of the evaluations Holter: approx. 15 MB (max. 60
MB)
ABPM: approx. 128 KB (max. 512 KB)
Holter-ABPM: approx. 20 MB (max. 25 MB)
Resting ECG: approx. 200 KB (for an ECG of approx. 10
seconds)
Stress ECG: approx. 6 MB (for an ECG of approx. 20 minutes)
CPET: refer to stress ECG
Spirometry: approx. 50 KB (max. 256 KB)
Rehab: approx. 6 MB (for approx. 45 minutes of exercise)
Hardware & ports DVD or CD-ROM drive,
USB port
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Recommended system requirements
Computer Intel Core i3-CPU with HD graphics 4400
4 GB RAM
256 GB SSD or SSHD (for single-position systems 2TB HDD)
1 GBit network connection (not for single-position systems)
Fanless Dual-DVI (or DP) graphics card (for CPET)
Windows 8.1 x64 (PRO version for joining a domain)
Ports One USB 2.0 port per USB device (preferably not USB
3.0)
One COM port each for ergometer and treadmills (serial)
At least Version 4.0 if Bluetooth is installed
otherwise can be deactivated in the BIOS
Monitor 20“ TFT with DVI or DP port
Full HD resolution
Dual-TFT for spiroergometry
Printer 600 dpi
Monochrome (colour recommended for spiroergometry)
USB 2.0 port or network connection
PCL-enabled (increases printing speed with the suitable
driver)
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2.8 Manufacturer's declaration regarding EMC (electromagnetic
compatibility) according to DIN EN 60601-1-2:2016
Lead lengthsPatient leads approx. 1450 mm (extremities) approx.
1200 mm (chest wall)USB cable approx. 3000 mm
Manufacturer's declaration – electromagnetic emissionsThe custo
cardio 400 BT ECG application system is designed for use in the
electromagnetic environment stated below. The customer or user of
custo cardio 400 BT should make sure that it is used in such an
environment.
Manufacturer’s declaration – electromagnetic immunity The custo
cardio 400 BT ECG application system is designed for use in the
electromagnetic environment stated below. The customer or user of
custo cardio 400 BT should make sure that it is used in such an
environment.
COMMENT: UT is the alternating supply voltage prior to
application of test levels
Emission measurements
RF emissions according to CISPR11
RF emissions according to CISPR11
Harmonics according to IEC61000-3-2
Voltage fluctuations/flickers according to IEC61000-3-3
Compliance
Group 1
Class B
Class A
Complies
Immunity tests
Static electricity discharge (ESD) according to IEC
61000-4-2
Quick transient electric interference factors / bursts according
to IEC 61000-4-4
Surgesaccording to IEC 61000-4-5
Voltage drops, brief interruptionsand fluctuations in supply
voltageaccording to IEC 61000-4-11
Magnetic field at supply frequency (50/60 Hz) according to IEC
61000-4-8
IEC 60601- test level
± 8 kV contact discharge± 15 kV air discharge
± 2 kV for net wires± 1 kV for input and Output leads
(SIP/SOP)
± 1 kV lead against lead± 2 kV lead against end
< 5 % UT for 0.5 periods(> 95 % drop)
40 % UT for 5 periods(60 % drop)
70 % UT for 25 periods(30 % drop)
< 5 % UT for 5 s(> 95 % drop)
30 A/m
Compliance level
± 8 kV contact discharge± 15 kV air discharge
± 2 kV for net wires± 1 kV for input and Output leads
(SIP/SOP)
± 1 kV lead against lead± 2 kV lead against end
< 5 % UT for 0.5 periods(> 95 % drop)
40 % UT for 5 periods(60 % drop)
70 % UT for 25 periods(30 % drop)
< 5 % UT for 5 s(> 95 % drop)
30 A/m
Electromagnetic environment - guidelines
custo cardio 400 BT uses the 2.4 GHz range frequency band to
communicate with the PC. Its level of RF emis-sion is therefore
very low and is unlikely to be sufficient to interfere with other
electronic devices.
custo cardio 400 BT is suitable for use in all establish-ments,
including domestic establishments and those di-rectly connected to
the public low voltage power supply network that supplies buildings
used for domestic pur-poses.
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Manufacturer’s declaration – electromagnetic immunityThe custo
cardio 400 BT ECG application system is designed for use in the
electromagnetic environment stated below. The customer or user of
custo cardio 400 BT should make sure that it is used in such an
environment.
1) The ISM bands (EN: Industrial, Scientific and Medical, i.e.
frequency bands used for industrial, scientific and medical
purposes) between 0.15 MHz and 80 MHz are 6.765 to 6.795 MHz;
13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz
to 40.70 MHz. The amateur radio bands between 0.15 MHz and 80 MHz
are 1.8 MHz to 2.0 MHz; 3.5 MHz to 4.0 MHz; 5.3 MHz to 5.4 MHz; 7
MHz to 7.3 MHz; 10.1 MHz to 10.15 MHz; 14 MHz to 14.2 MHz; 18.07
MHz to 18.17 MHz; 21 MHz to 21.4 MHz; 24.89 MHz to 24.99 MHz; 28
MHz to 29.7 MHz and 50 MHz to 54.0 MHz.
COMMENT on the tableRow 2: Applies for all other connections
(patient leads, power supply unit, USB cable)Row 3: Applies for the
custo cardio 400 BT housing
Immunity tests
Conducted disturbances, induced by high-frequency fields
according to IEC61000-4-5
Radio-frequency electromagnetic fields
according to IEC61000-4-3
IEC 60601- test level
3 Veffective value
0.15 MHz to 80 MHz
6 Veffective value
in ISM frequency bands1)
between 0.15 MHZ and 80 MHz
80 % AM at 1 kHz
3 V/m
80 MHz to 2.7 GHz
80 % AM at 1 kHz
Compliance level
3 Veffective value
0.15 MHz to 80 MHz
6 Veffective value
in ISM frequency bands1)
between 0.15 MHZ and 80 MHz
80 % AM at 1 kHz
10 V/m
80 MHz to 2.7 GHz
80 % AM at 1 kHz
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Recommended protective distances between portable and mobile RF
telecommunication devices and custo cardio 400 BTcusto cardio 400
BT is designed for use in an electromagnetic environment in which
the RF transients can be controlled. The user can help avoid
electromagnetic interference by maintaining the minimum distance
between portable and mobile RF telecommunication devices
(transmitters) and the device – depending on the power output of
the communication device, as indicated below.
WARNING: Wearable RF communication devices (radio devices)
(including their accessories, e.g. antenna cables and external
antennas) should not be used at distances of less than 30 CM (12
inches) from the custo cardio 400 BT parts and leads described by
the manufacturer. Failure to observe this warning can compromise
the per-formance of the device.
WARNING: Use of this device directly next to other devices or
stacked together with other devices should be avoided, as this
could result in fault operation. If the devices must nonetheless be
used as described above, this device and the other devices should
be monitored to ensure proper functionality.
a) For some radio services, on the frequencies for the radio
connection of mobile communication devices to the base station
(uplink) were included in the table.
COMMENT on protection clearances: The minimum clearances for
increased immunity test levels must be calculated using the
following equation:
where P is the maximum output in Watt (W), d the minimum
clearance in metres (m) and E the immunity test level in Volt per
metre (V/m).
General COMMENTS: These guidelines may not apply in every case.
The propagation of electromagnetic variables is influenced by
absorptions and reflections of buildings, objects and people.
Frequency banda) MHz
380 to 390
430 to 470
704 to 787
800 to 960
1700 to 1990
2400 to 2570
5100 to 5800
Radio servicea)
TETRA 400
GMRS 460, FRS 460
LTE Band 13, 17
GSM 800/900,TETRA 800, iDEN 820,
CDMA 850, LTE Band 5
GSM 1800, CDMA 1900,GSM 1900, DECT,
LTE Band 1, 3, 4, 25,UMTS
Bluetooth, WLAN 802.11 b/g/n
RFID 2450, LTE Band 7
WLAN 802.11 a/n
Maximum output in W
1.8
2
0.2
2
2
2
0.2
Clearance in m
0.3
0.3
0.3
0.3
0.3
0.3
0.3
Immunity test level in V/m
27
28
9
28
28
28
9
� � 6d∗ √P
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2.9 EC Declaration of Conformity
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Set no. Set name Part no. Qty. Set/product designation
85130 custo cardio 400 BT
84024 1 custo cardio 400 BT ECG application system
85034 6 Thoracic wall leads (1.20 m)
85035 4 Extremity leads (1.45 m)
85027 2 Pck.10 Electrode “hair”
85032 2 Spacer 2-fold
85033 2 Spacer 3-fold
85060 1 Telescopic boom for custo cardio 400 BT
with velcro fasteners and hex key
85073 1 Bracket for telescopic boom
85070 1 Cable hook for custo cardio 400 BT
55050 1 Bluetooth 4.0 USB adapter LM506
16018 1 1.8 m USB extension cable connector A – power outlet
A
85023 BET-0612 power supply unit for custo cardio 400, 12 V, 5
A
85044 Power supply cable for power supply unit BT, 1 m
85031 1 3 m USB cable for custo cardio 400 BT
2.10 List of product components and accessories
Accessories Part no. Set/product designation
85027/Z Electrode “hair” (bag of 10 pieces)
85064/Z Electrode “standard” (bag of 10 pieces)
85065/Z Electrode “small” (bag of 10 pieces)
85035/z Extremity lead (1.45 m)
85034/z Thoracic wall leads (1.20 m)
85061 Extra long suction lead (1.65 m)
85032 Spacer 2-fold
85033 Spacer 3-fold
85036/z Coding set (1 sheet of 10 pieces)
85070 Cable hook for custo cardio 400 BT
85060 Telescopic boom for custo cardio 400 BT
85081 Telescopic boom for trolley custo easy plus
85073 Bracket for telescopic boom including fixtures
85068 Universal bracket for custo cardio 400 BT
85079 Wall mounting set for custo cardio 400 BT
85037 BET-0612 M power supply unit 12 Volt for custo cardio 400
BT
85038 Black 1.5 m power supply cable for power supply unit
BET-0612
85047 Power supply unit VEC50US15, 15 Volt für custo cardio
400
85044 Power supply cable for power supply unit VEC50US15, 1
m
85044-5 Power supply cable for power supply unit VEC50US15, 5
m
85031 3 m USB cable for custo cardio 400 BT
55050 Nano Bluetooth USB adapter
85056 Clamp adapter socket 4 mm f. connection to patient
simulator (5 pcs.)
85057 Adapter for patient simulator (10 pcs.)
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Manufacturer's contact details:custo med GmbHMaria-Merian-Straße
685521 OttobrunnGermany
Phone: +49 (0) 89 710 98 - 00Fax: +49 (0) 89 710 98 - 10E-mail:
[email protected]: www.customed.de