D
General provisions
1.
Explanation of symbols
0123
This unit corresponds to the Council Directive 93/42/EEC from
14 June 1993 about medical products and bears the sign CE 0123
(TÜV SÜD Product Service GmbH)
Devices with CE marking are quality-controlled according to this
directive and provide higher accuracy than the former calibration.
Degree of protection against electric shock: TYPE BF
Please note operating manual
Storage and transport conditions ambient temperature
-25 to 55°C (-13°F to 131°F)
Protect against moisture/humidity
Rel. air humidity 15% - 95%
Keep dry
Manufacturer
2.
Disposal
Batteries and technical devices are not household waste and must
be delivered to the corresponding collection and disposal sites.
EN-46
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General provisions
3.
Electromagnetic compatibility (EMC)
Technical description
The unit complies with the EMC requirements of the international standard
EC60601-1-2. The requirements are fulfilled under the conditions described in the
following.
The unit is an electric medical product and is subject to special precautions with
respect to EMC that must be published in the operating manual.
Portable and mobile HF communication facilities can affect the unit. Use of the unit
with accessories not approved can affect the unit in a negative way and change
the electromagnetic compatibility.
The unit should not be used immediately next to or between other electric devices.
Table 201 - Guidance and manufacturer's declaration - electromagnetic emissions
Emissions test
Compliance
RF emissions CISPR 11
Group 1
RF emissions CISPR 11
Class B
Harmonic emissions
N/A
IEC 61000-3-2
Voltage fluctuations/Flicker emissions
N/A
IEC 61000-3-3
D
Electromagnetic environment - guidance
The device 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.
EN-47
06.08.2009 20:47:44