Medel Dualstetho PRO Handleiding

Medel Bloeddrukmeter Dualstetho PRO

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ANEROIDS
USER MANUAL
ANEROIDS BLOOD PRESSURE DEVICE
INDEX
1. INTRODUCTION...............................................................1
2. WARNING...........................................................................1
3. COMPONENTS OF MEDEL ANEROID............................1
4. WORKING PRINCIPLES....................................................1
5. CARRYING OUT A MEASUREMENT...............................2
6. HOW TO USE THE BLOOD PRESSURE MONITOR.......2
7. IMPORTANT RECOMMENDATIONS..............................2
8. MANTAINANCE AND CARE ............................................3
9. SERVICING AND GAUGING.............................................3
10. TECHNICAL SPECIFICATIONS........................................3
11. WARRANTY CONDITIONS...............................................3
1. INTRODUCTION
ank you for buying a MEDEL aneroid blood-pressure monitor. is blood-pressure monitor works
according to the Riva Rocci/Korotko auscultating method.
MEDEL has a complete range of aneroid blood-pressure monitors with dierent features according to
their usage: home, or doctor’s practice.
Each MEDEL blood-pressure monitor is gauged and undergoes an accurate quality control.
Before usage read carefully and entirely this instruction manual and keep it in a safe place.
Please, check equipment and product characteristics described on the box.
2. WARNING
To carry out a measurement with the auscultating method requires a specic knowledge of this technique.
Incidental wrong interpretations and damages which can result from wrong usage cannot be ascribed
to the device.
is device is not a diagnostic device but a measurement system.
e measurement results must be evaluated by a doctor.
Auscultating method blood-pressure monitors are not recommended to persons with hearing problems.
3. COMPONENTS OF MEDEL ANEROID
MEDEL aneroid blood-pressure monitors consist in (Pic. 1):
4. WORKING PRINCIPLES
MEDEL aneroid blood-pressure monitors work according to the Riva Rocci/Korotko auscultating
method.
Measurement is carried out by occluding the radial artery through the pressure of a mu wrapped around
one arm (cu) and the following observation of the heart pulse tones (with the stethoscope) during the
deating phase.
It is reccomended to use the following points for auscultation:
• K5 in auscultation of adults
• K4 in auscultation of children aged 3 to12
• K5 in pregnant female patients, unless sounds are audible with cu deated, in which case K4
Pic.1
should be used (K5 is the point at which Korotko
sounds can no longer be heard; K4 is the change in the
tones heard through a stethoscope from a clear tapping
sound to a mued sound.)
In case of doubts about the method consult your doctor.
e latex bulb enables to generate the necessary air pressure
inside the cu in order to occlude the radial artery. e release
valve allows an accurate regulation of the air outlet from the
cu, permitting a gradual deation.
e stethoscope (furnished only with some models) allows to
survey the heart pulse tones.
Each manometer has a reading scale ranging from 0 to 300
mmHg (mmHg=millimeters of mercury). e scale is traced
every 2mmHg, with larger notches every 10mmHg for an easy
reading.
e measurement has a precision of +- 3mmHg.
5. CARRYING OUT A MEASUREMENT
Before the measurement:
• Avoid eating, smoking as well as any form of exertion before the measurement. All these factors
inuence the measurement results. Try to relax by sitting in an armchair in a quiet atmosphere
for about ten minutes before the measurement.
• Remove any garment that ts closely to your upper arm.
• Measure always on the same arm (normally le).
• Try to carry out the measurements regularly at the same time of day, as the blood-pressure chan-
ges during the course of the day.
Common sources of error:
Note: Comparable blood-pressure measurements require always the same conditions !
ese are normally quiet conditions.
• All eorts by the patient to hold up the arm can increase the arterial pressure. Make sure to sit
down in a comfortable, relaxed position, with legs uncrossed and not to activate any muscle of
the measurement arm during the measurement. Use a cushion for support if necessary.
• If the arm artery lies considerably lower (higher) than the heart, an erroneously higher (lower)
bloodpressure will be measured.
• Cus that are too narrow or too short result in false measurement values.
• Selecting the correct cu is very important. e cu size depends on the arm circumference
(measured in the middle). e permissible range is printed on the cu. If this is not suitable for
your arm, please contact your dealer.
• Use only Medel original cus !
• e device is furnished with a standard adult cu for arms of circumference between 26-38 cm.
6. HOW TO USE THE BLOOD PRESSURE MONITOR
Make sure the cu is completely at. Fasten the cu on the upper part of the learm, making sure that
the tubing is facing downwards. If the device is provided with D-ring (please, check
the equipment on the box) put on the cu, place it in the correct way, pull the cu
lewards sliding it inside the metal bracket and x it to the velcro. (Pic. 2).
e lower edge of the cu must be at least 2 centimeters above the elbow, at heart’s
height (Pic. 3). ere should be enough space between cu and arm to t a nger
inside.
e arrow in the cu label must be in correspondance with the radial artery.
e stethoscope diaphragm should lie on the pulse position. Ask your doctor to
show it if necessary. Take the bulb and make sure that the pressure-release valve
is closed (turn it clockwise). nate the cuby squeezing the bulb, keep pumping I
until you reach 20-30mmHg beyond the highest expected pressure.
Slowly deate the cu turning the pressure-release valve anticlockwise, to obtain a
pressure decrease of 2- 3mmHg per second.
e rst audible tone corresponds to the highest (or systolic) pressure and the last
one corresponds to the lowest (or diastolic) pressure.
Open the release valve in order to deate completely the
cu. If it is necessary to interrupt a blood pressure measurement for any reason
(e.g. if the patient feels unwell), deate immediately the cu by opening completely
the release valve.
7. IMPORTANT RECOMMENDATIONS
• Never let air in beyond 300mmHg.
• e time used to measure blood pressure must not exceed 2 minutes.
Pic.3
Pic.2
2-3 cm
cu edge
tube
• Never make a second measurement before at least 5 minutes aer the rst one.
• Do not drop the device and handle it with care.
• Avoid strong vibrations.
• Do not expose the device to either extreme temperatures, humidity, dust or direct sunlight.
• Keep the device at a temperature between 10 and 40°C with a relative humidity not exceeding
85%.
• Keep the device and especially the rubber parts away from UV rays.
• Beware of damaging the rubber parts with sharp, cutting objects.
• Do not excessively bend the cu and the tubings.
• Clean the device with a so, dry cloth. Do not use petrol or solvents.
• Never open the device !
8. MANTAINANCE AND CARE
1) Manometer:the manometer requires no maintenance. If necessary, address to an authorized techni-
cal service centre or to your own dealer.
2) Bulb: if you have to replace the bulb make sure that the connecting parts are completely dry and clean
so that they can rmly hold together. You will thus avoid any air leak.
3) Cu: before cleaning the cu, remove the inner tube and close the velcro (placing the metal ring
inside in case of D-ring models). e cu can be washed at 30°C with a programme and a detergent
for delicate clothes.
DO NOT IRON.
You can also clean the cu with a sponge or a so brush and a detergent for delicate clothes. Rinse with
water.
9. SERVICING AND GAUGING
Each Medel blood-pressure monitor is gauged before being commercialized.
No recalibration is required.
Never open the device !
ere are no user-serviceable parts. e device requires no lubrication or maintenance.
In case of misfunctioning, address to MEDEL CUSTOMER SERVICE.
10. TECHNICAL SPECIFICATIONS
Storage and transportation conditions : -20 to +70°C
Humidity: 15 to 85% relative humidity (non-condensing)
Operation temperature: 10 to 40°C
Measuring method: auscultating method
Measuring range: 0 to 300 mmHg
Accuracy: ± 3 mmHg
Accessories: check equipment and product characteristics described on the box.
Medical Device Im Class (with measuring function)
e device complies with:
EU Medical Devices Directive 93/42/EEC and following amendments
Standards EN ISO 81060-1:2012 Non-invasive sphygmomanometers -- Part 1: Requirements and test
methods for non-automated measurement type.
11. SYMBOLS WARRANTY CONDITIONS
12. WARRANTY CONDITIONS
• The device is covered by a 2- year warranty from date of purchase for any defects in the
design or in the material used.
• -The warranty consists in the replacement and/or repair free of charge of originally de
tective components.
• The warranty does not cover the accessories supplied with the equipment and those parts
subject to normal wear and tear.
• The equipment must be repaired by authorized technical service centres only.
• The equipment must be sent to the authorized technical service centre for repair within 8
days after the defect is noticed.
• The transport costs for the equipment are at user’s charge. Any repair out of the warranty
conditions are at user’s charge.
• The warranty does not cover failures resulting from misuse, abuse of the product or in
case the damage is not due to manufacturer’s liability (accidental fall, rough transpor-
tation, etc…)
• The warranty does not involve any compensation for any kind of damages to persons or
things, either direct or indirect, occurred when the equipment is not operating.
• The warranty is valid from the date of purchase certified by the ticket or the invoice which
have to be peremptorily attached to the warranty coupon.
• -The lack of warranty coupon properly filled in and validated by a certification of purcha
se voids the warranty.
!
MANUFACTURER
0197
The CE labelling certifies that the product complies with the essential requirements of
Directive 93/42/EEC on medical products.
LOT
Batch number
SN
Serial number
EC REP
Authorised Representative in the Euro-
pean Community
REF
Manufacturer’s catalogue device number
WARNING
0197
REV.02_SEPTEMBER 2019_CODE 100201
1 32

Product specificaties

Merk: Medel
Categorie: Bloeddrukmeter
Model: Dualstetho PRO

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