u l C l A s s i f i C A t i o N
EN-14
e l e C t r o M A G N e t i C C o M P A t i b i l i t Y
eLeCtrOmAgnetiC COmpAtiBiLitY infOrmAtiOn ACCOrding tO ieC/en 60601-1-2
table 1 for emissions
guidAnCe And mAnufACturer’s deCLArAtiOn –
eLeCtrOmAgnetiC emissiOns
The GRPro
™
2.1 is intended for use in the electromagnetic environment specified below. The
customer or the user of the GRPro
™
2.1 should assure that it is used in such an environment.
Emissions tEst
ComplianCE
ElECtromagnEtiC EnvironmEnt – guidanCE
RF emissions CISPR 11
Group 1
The GRPro
™
2.1 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 GRPro
™
2.1 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.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions IEC
61000-3-3
Complies
EN-15
protection against electric shock (5.1):
The GRPro System is considered to be Class I (protective earth) when connected to the
FSP Group, Inc. model FSP 030-RCAM power supply. The GRPro System is considered
to be Class II (double insulated) when connected to the GlobTek Model GTM-21097-5012
power supply.
protection against harmful ingress of water (5.3):
This product provides ordinary protection against ingress of water.
degree of safety in the presence of flammable anesthetics or oxygen (5.5):
Not suitable for use in an oxygen enriched environment or in the presence of flammable
anesthetics.
electromagnetic interference:
This equipment has been tested and found to comply with the limits for medical devices
in IEC 60601-1-2:2001. These limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This equipment generates, uses and
can radiate radio frequency energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other devices in the vicinity. However,
there is no guarantee that interference will not occur in a particular installation. If this
equipment does cause harmful interference to other devices, which can be determined by
turning the equipment off and on, the user is encouraged to try to correct the interference
by one or more of the following measures:
•
Reorient or relocate the receiving device.
•
Increase the separation between the equipment. Connect the equipment into an outlet
on a circuit different from that to which the other device(s) are connected.
•
Consult the manufacturer or field service technician for help.
Medical Equipment
With respect to electrical shock, fire, and mechanical hazards only in
accordance with UL 60601-1, CAN/CSA C22.2 No. 601.1
Powered by Direct Current
Type BF Applied Parts
Attention: Consult accompanying documents before use.
Manufacturer
SUPERSEDED
