21
8. Error messages / troubleshooting
In case of faults, the _ message appears in the display.
Error messages can occur when
1. It was not possible to record the pulse
E1
,
2. You move or speak during the measurement
E2
,
3. The cuff is fastened too tightly or loosely
E3
,
4. Errors occur during the measurement
E4
5. The pump pressure is higher than 300 mmHg
E5
6. The batteries are almost empty
E6
In the above cases, you must repeat the measurement. Make
sure that the cuff tube is properly inserted and that you do
not move or talk. Re-insert the batteries if necessary, or else
replace them.
9. Specifications
Model no.
SBM 36
Measurement
method
Oscillometric, non-invasive blood pres-
sure measurement on the upper arm
Measurement range
Cuff pressure 0 – 300 mmHg,
systolic 50 – 250 mmHg,
diastolic 30 – 200 mmHg,
Pulse 40 – 180 beats/minute
Display accuracy
Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Measurement inac-
curacy
Max. permissible standard deviation
according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
Memory
2 x 60 memory spaces
Dimensions
L 98 mm x W 140 mm x H 53 mm
Cuff size
22 to 36 cm
Permissible operating
conditions
+10 °C to +40 °C, 30%- 85 % relative air
humidity (non-condensing)
Permissible storage
conditions
- 20 °C to +60 °C, 10%-95% relative air
humidity, 700 –1060 hPa ambient pres-
sure
Power supply
4 x 1,5 V
AAA batteries
Battery life
For approx. 500 measurements,
depending on the blood pressure level
and/or pump pressure
Accessories
Instruction for use, 4 x 1.5 V AAA batter-
ies, storage pouch
Classification
Internal supply, IPX0, no AP or APG,
continuous operation, type BF applied
part
Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601-1-2 and
is subject to particular precautions with regard to electro-
magnetic compatibility (EMC). Please note that portable and
mobile HF communication systems may interfere with this
unit. More details can be requested from the stated Customer
Service address or found at the end of the instructions for use.
• This device is in line with the EU Medical Devices Direc-
tive 93/42/EC, the „Medizinproduktegesetz“ (German Medi-
cal Devices Act) and the standards EN 1060-1 (non-inva-
sive sphygmomanometers, Part 1: General requirements),
