® BPM68 ® BPM68
EMC Tables
EVOCHECK® Blood Pressure Monitor BPM8 is intended for use in the electromagnetic
environment specied below. The customer or the user of EVOCHECK® Blood Pressure Monitor
BP68 must make sure that it is used in such an environment.
Guidance and manufacturer’s declaration - Electromagnetic emissions
Phenomenon Professional healthcare facility Home Healthcare
environment a) environment a)
Conducted and radiated a) CISPR 11
RF EMISSIONS Group 1 Class B
Harmonic distortion Not applicable
Voltage uctuations Not applicable
and ickering
a) The equipment is suitable for use in Home Health Environments and Professional Health Care Environments
limited to patient rooms and respiratory treatment facilities in hospital or clinics. The more restrictive
acceptance limits of Group 1 Class B (CISPR 11) have been considered and applied. The equipment is suitable
for use in the mentioned environments when directly connected to the Public Mains Network.
b) The test is not applicable in this environment unless the ME EQUIPMENT and ME SYSTEM used will be connected
to the PUBLIC MAINS NETWORK and the power input is otherwise within the scope of the Basic EMC standard.
Guidance and manufacturer’s declaration - Electromagnetic immunity - Enclosure port
Phenomenon Basic EMC mmunity test levels
standard or test method Professional healthcare HOME HEALTHCARE
facility environment ENVIRONMENT
ELECTROSTATIC IEC 61000-4-2 ± 8kV contact
DISCHARGE ± 2 kV, ±4kV ±, ±8 kV, ±15 kV air
Radiated RF EM elds IEC 61000-4-3 a)
10 V/m b) 80MHz - 2.7
GHz 80% AM at 1kHz
Proximity elds from RF IEC 61000-4-3 COMPLIANT
wireless communications NOTE: Further information about distances to
equipment be maintained between portable and mobile
RF communications equipment (transmitters)
and the EVOCHECK® Blood Pressure Monitor
BP68 can be requested from EVOCHECK® Blood
Pressure Monitor using the contact information
provided in this manual. However, it is advisable
to keep the electromechanical aerosol equipment
at an adequate distance of, at least, 0.5 m from
mobile phones or other RF communications
transmitters to minimise possible interference.
RATED power frequency IEC 61000-4-8 30 A/m c)
magnetic elds. 50 Hz or 60 Hz
a) The equipment is suitable for use in Home Health Environments and Professional Health Care Environments
limited to patient rooms and respiratory treatment facilities in hospital or clinics. The more restrictive IMMUNITY
acceptance limits have been considered and applied.
b) Before modulation is applied.
c) This test level assumes a minimum distance of at least 15 cm between the ME EQUIPMENT or ME SYSTEM and
sources of power frequency magnetic elds.
18 19
Explanation of Symbols
Disposal information: Should you wish to dispose of the article, do so
in accordance with current regulations. Details are available from your
local authority
“ON/OFF” (push-push)
Type of protection of applied part against electric shock, body oating
This product meets the basic safety and essential performance
requirements indicated in the IP22 conditioning test (protection
against solid foreign objects of 12.5mm ø and greater and against
vertically falling water drops when enclosure tiled up to 15°)
Temperature limits
European Authorized Representative
Manufacturer’s name and address
SN YYMWWWXXXXX
SN: Product Serial Number
YY: year, M:month, WWW: working sheet, XXXXX:
serial no.
Follow instructions for use
IP22
SN
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