1.User A
3.Movement error symbol
5.Cuff self-detecting function
7.PM symbol
9.WHO function symbol
11.Average value symbol
13.Pulse symbol
15.Minute symbol
17.Month symbol
19.Systolic blood pressure
2.User B
4.Mute symbol
6.AM symbol
8.Low battery symbol
10.Heartbeat symbol (Flashes during measurement)
12.NO. symbol
14.Date symbol
16.Diastolic blood pressure
18.Hour symbol
Features of Model C02
2. Double users: 2 x 120 sets memory
4. Low battery display
6. Auto power-off
8. Time stamp in memory
1. Cuff self-checking function
3. Average value function
5. WHO function
7. External power adapter support
Setting the Year/Month&Date/Time:
Long press the SET button for more than 6s, and then you can start to set.
Setting the Year:
Initial year is 2022, when the year display is flashing, press the MEM button, the
year will increase by I year each, hold the MEM button and it will increase
continuously 1 by 1, until 2049, and then rollover to 2022, once the year set is OK,
press SET button to confirm.
Setting Month/Date:
Initial Month/Date is 01/01, when the Month display is flashing, press the MEM
button, the month will increase by 1, press SET button to confirm, and do in the
same way to set the date. Press SET button to confirm.
Setting Time :
When the hour display is flashing, press the MEM button, the hour will increase
by 1, press SET button to confirm, and do in the same way to set the minute.
Press SET button to confirm.
Shenzhen Jamr Technology Co., Ltd.
A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road,
Guixiang Community, Guanlan Street, Longhua District, 518100 Shenzhen,
PEOPLE'S REPUBLIC OF CHINA
The device is a fully automatic blood pressure monitoring device,it is intended to
measure the systolic and diastolic blood pressure as well as the pulse rate by using
the oscillometric method.
The device is used for adult that ages are more than 12 years old,and used for
over-the-counter,it can be used in medical facilities and at home.
(For eco-friendly and transport safe, batteries
and adapters are not included in the product package.)
1
2 3 4 5 6 7
8
15
14
13
12
11
9
10
16
17
18
19
Disclaimer regarding the blood pressure monitor, the device is Over-the-Counter
(OTC), and the measurements are for informational purposes only and are not
intended to diagnose, treat, cure or prevent any disease or health condition.
Reminder.
The model number of this device is: C02
Has been approved by FDA, certification 510K number: K200437
In order to get more accurate measurement results, please pay attention to the
correct measurement requirements.
LEGAL DISCLAIMER
成品尺寸90*130MM，
展开尺寸630*130MM，材质：80G书写纸，双面折页
SET
SET
Note:
If you decide to delete the all memory, please keep the memory in another way,
incase you need it some days later. Take the battery out won’ t lead to a memory
missing.
1) Press "SET" button to select the user.
2) Press "MEM" button to view the user's history.
3) Hold down the "MEM" button for three seconds. All records associated with the
user will be erased.
Blood pressure category Systolic mmhg Diastolic mmhg
Best ≤119 ≤79
Normal 120-129 80-84
Elevated 130-139 85-89
High Blood Pressure(Hypertension)Stage 1 140-159 90-99
High Blood Pressure(Hypertension)Stage 2 160-179 100-109
Hypertension Crisis(consult your doctor immediately) ≥180 ≥110
WHO
American
Weak battery or improper placement
Sensor abnormal
Replace both batteries with new ones. Check the
battery installation for proper placement of the
battery polarities.
Please make sure the cuff pressure is drained and
then measure again. If the error is still displayed,
please send it to local distributor
Tie the cuff correctly and make the measurement
again. If the error is still displayed, please send it to
local distributor
Occasionally-measure for one more time/ Always -
send it to local distributor
Tie the cuff correctly and make sure the air plug is
properly inserted in the unit
Correct it and make the measurement again
Please keep quiet and don’t move
Please send back to the local distributor
Please send back to the local distributor
Monitor could not detect pulse wave or
cannot calculate the blood pressure data
Measurement result is abnormal
Too loose cuff or air leakage
The air tube is crimped or the cuff is tied too
tight.
The sensor is sensing great fluctuation in the
pressure
The pressure that the sensor sensing is over
the limit
The demarcation is incorrect or the device
has not been demarcated
HI Beyond the measurement range, normal reminder The pulse rate exceeds the upper limit (>170
per minute)
LO Beyond the measurement range, normal reminderThe pulse rate is less than the lower limit (<40
per minute)
MR unsafe.
Guidance and manufacturer’s declaration - electromagnetic emissions
Emissions test
RF emissions CISPR 11
Compliance
Group 1
RF emissions CISPR 11 Class B
Harmonic emissions IEC 61000-3-2
Class A
Applied
Voltage fluctuations/ flicker emissions IEC 61000-3-3
Guidance and manufacturer’s declaration - electromagnetic Immunity
Test frequency
30 kHz
IMMUNITY TEST LEVEL (A/m)
8
134,2 kHz 65
c)
13,56 MHz
Modulation
CW
Pulse modulation
b)
2,1 kHz
Pulse modulation
b)
50 kHz
75
c)
a) This test is applicable only to ME EQUIPMENT and ME SYSTEMS intended for use in the HOME HEALTHCARE ENVIRONMENT.
b) The carrier shall be modulated using a 50 % duty cycle square wave signal.
c) r.m.s., before modulation is applied.
Guidance and manufacturer’s declaration - electromagnetic Immunity
Immunity Test IEC 60601-1-2 Test level Compliance level
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency magnetic
field IEC 61000-4-8
30 A/m
50Hz/60Hz
30 A/m
50Hz/60Hz
Conduced RF
IEC61000-4-6
150KHz to 80MHz：3Vrms
6Vrms (ISM and amateur radio bands)
80% Am at 1kHz
150KHz to 80MHz：3Vrms
6Vrms (ISM and amateur radio bands)
80% Am at 1kHz
Radiated RF
IEC61000-4-3
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
Proximity magnetic
fields
IEC 61000-4-39
30 kHz: 8A/m
134.2 kHz: 65A/m
13.56 MHz: 7.5A/m
30 kHz: 8A/m
134.2 kHz: 65A/m
13.56 MHz: 7.5A/m
0% 0.5 cycle
At 0º, 45 º, 90 º, 135 º, 180 º, 225 º, 270 º
and 315 º
0% 1 cycle And 70% 25/30 cycles
Single phase: at 0
0% 300 cycle
0% 0.5 cycle
At 0º, 45 º, 90 º, 135 º, 180 º, 225 º,
270 º and 315 º
0% 1 cycle And 70% 25/30 cycles
Single phase: at 0
0% 300 cycle
±8 kV contact
±2 kV, ±4 kV, ±8 kV,
±15 kV air
Power supply lines：±2 kV
input/output lines：±1 kV
100 kHz repetition frequency
line(s) to line(s)：±0.5 kV
line(s) to earth：±2 kV
line(s) to lines(s): ±1 kV
±8 kV contact
±2 kV, ±4 kV, ±8 kV,
±15 kV air
Power supply lines：±2 kV
line(s) to line(s)：±0.5 kV
line(s) to line(s)：±1 kV.
NOTE 1: U
T
is the a.c. mians voltage prior to application of the test level.
Guidance and manufacturer’s declaration - electromagnetic Immunity
If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna and the ME
EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m test distance is permitted by IEC 61000-4-3.
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, the carrier may be pulse modulated using a 50 % duty cycle square wave signal at
18 Hz. While it does not represent actual modulation, it would be worst case.
Test
Frequency
(MHz)
Band
(MHz)
Service Modulation
IMMUNITY
TEST LEVEL
(V/m)
385
450
710
745
780
810
870
930
430-470 GMRS 460,
FRS 460
FM
±5 kHz deviation
1 kHz sine
380-390 TETRA 400 Pulse modulation
18 Hz
27
28
28
28
28
9
9
704-787
800-960
1700-1990
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
Pulse
Modulation
18 Hz
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz
1720
1845
1970
2450 2400-2570
5100-5800
Bluetooth,
WLAN,
802.11 b/g/n,
RFID 2450,
LTE Band 7
WLAN 802.11
a/n
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz
5240
5500
5785
a)
b)
b)
b)
b)
b)
b)
c)
a)
a)
Radiated RF
IEC61000-4-3
(Test
specifications
for ENCLOSURE
PORT
IMMUNITY
to
RF wireless
communication
s equipment)
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments
and so on.
Warning: Don’t near active HF surgical equipment and the RF shielded room of an
ME system for magnetic resonance imaging, where the intensity of EM
disturbances is high.
Warning: Use of this equipment adjacent to or stacked with other equipment
should be avoided because it could result in improper operation. If such use is
necessary, this equipment and the other equipment should be observed to verify
that they are operating normally.
Warning: Use of accessories, transducers and cables other than those specified
or provided by the manufacturer of this equipment could result in increased
electromagnetic emissions or decreased electromagnetic immunity of this
equipment and result in improper operation.”
Warning: Portable RF communications equipment (including peripherals such
as antenna cables and external antennas) should be used no closer than 30 cm
(12 inches) to any part of the Blood Pressure Monitor (C02), including cables
specified by the manufacturer. Otherwise, degradation of the performance of
this equipment could result.
If any: a list of all cables and maximum lengths of cables (if applicable),
transducers and other ACCESSORIES that are replaceable by the RESPONSIBLE
ORGANIZATION and that are likely to affect compliance of the ME EQUIPMENT or
ME SYSTEM with the requirements of Clause 7 (EMISSIONS) and Clause 8
(IMMUNITY). ACCESSORIES may be specified either generically (e.g. shielded
cable, load impedance) or specifically (e.g. by MANUFACTURER and EQUIPMENT
OR TYPE REFERENCE).
If any: the performance of the ME EQUIPMENT or ME SYSTEM that was
determined to be ESSENTIAL PERFORMANCE and a description of what the
OPERATOR can expect if the ESSENTIAL PERFORMANCE is lost or degraded due
to EM DISTURBANCES (the defined term “ESSENTIAL PERFORMANCE” need not
be used).
Technical description
1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL
PERFORMANCE with regard to electromagnetic disturbances for the excepted
service life.
2. Guidance and manufacturer’s declaration -electromagnetic emissions and
Immunity
Table 3
Table 2
Table 1 Table 4
