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InfoBionic MoMe 01854 User Manual

InfoBionic MoMe 01854
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page 16
Electromagnetic Emissions Compliance
The MoMe
®
Kardia monitor has been tested and found to comply
with the limits for medical devices to the IEC 60601-1-2:2007.
These limits are designed to provide reasonable protection against
harmful interference in a typical installation.
1. This device radiates radio frequency energy in normal use and, if
not installed and used in accordance with instructions in this manual,
may cause harmful interferences to other devices in the vicinity.
If this device does cause harmful interference to other devices,
the user is encouraged to try to correct the interference by one or
more of following measures:
— Reorient or relocate the other device/s
— Increase the separation distances between this device
and other device/s
— Consult the manufacturer/s of other device/s or call
service for help
2. The device performance may be affected by heavy electrical
equipment or other sources of electromagnetic interference.
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
The MoMe
®
Kardia is intended for use in the electromagnetic environment
specified below. The customer or the user of MoMe
®
Kardia should assure
that it is used in such an environment
Emissions Test
Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The MoMe
®
Kardia uses RF energy only for its
internal function. Therefore, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions
CISPR 11
Class B The MoMe
®
Kardia is suitable for use in
all establishments, including domestic
establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings used
for domestic purposes.

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InfoBionic MoMe 01854 Specifications

General IconGeneral
BrandInfoBionic
ModelMoMe 01854
CategoryMedical Equipment
LanguageEnglish