38
Explanation of symbols
Electromagnetic Compatibility Information
The device satisfies the EMC requirements of the international standard IEC
60601-1-2. The requirements are satisfied under the conditions described in the
table below. The device is an electrical medical product and is subject to special
precautionary measures with regard to EMC which must be published in the in-
structions for use. Portable and mobile HF communications equipment can affect
the device. Use of the unit in conjunction with non-approved accessories can af-
fect the device negatively and alter the electromagnetic compatibility. The device
should not be used directly adjacent to or between other electrical equipment.
Table 1
Guidance and declaration of manufacturer-electromagnetic emissions
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic environment - guidance
Radiated emission
CISPR 11
Group 1,
class B.
The device uses RF energy only for its internal
function. Therefore, its emissions are very low
and are not likely to cause any interference in
nearby electronic equipment.
Conducted emission
CISPR 11
Group 1,
class B.
The device is suitable for use in all establish-
ments, including domestic establishments and
those directly connected to the public low-volt-
age power supply network that supplies build-
ings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/ flicker
emissions IEC 61000-3-3
Complies
ENGLISH
Caution: read
instructions (warnings)
carefully
Authorized represent-
ative in the European
community
Medical Device com-
plies with Directive
93/42/EEC
WEEE disposal
Keep away from
sunlight
Serial number
Product code
Lot number
Direct Current
Manufacturer
Date of manufacture
Humidity limit
Temperature limit
Follow instructions
for use
Type BF applied part
IP21 Covering Protection
rate
