Guidelines And Tables On Electromagnetic Compatibility - Medizintechnik MASTERLIGHT Serie Instrucciones De Empleo

Guidelines and tables on electromagnetic compatibility.

KaWe examination lights require special precautions related to electromagnetic compatibility (EMC) and must be installed in
accordance with the EMC guidelines included in the accompanying documents. The performance of the examination lights can be
affected by portable and mobile HF telecommunication devices.
Guidelines and tables on electromagnetic compatibility.
The use of non-KaWe accessories or spare parts will result in increased emissions or reduced immunity of the device.
ght spots of KaWe examination lights require special precautions related to electromagnetic compatibility (EMC) and must be installed in
tersection accordance with the EMC guidelines included in the accompanying documents. The performance of the examination lights can be
affected by portable and mobile HF telecommunication devices.
For proper operation of the examination light, it is necessary to prevent its placement in the immediate vicinity of other
r of the
The use of non-KaWe accessories or spare parts will result in increased emissions or reduced immunity of the device.
devices or on top of each other, and if it is required to operate it in the immediate vicinity of other devices or on top of
g
each other, it is necessary to monitor the examination light.
For proper operation of the examination light, it is necessary to prevent its placement in the immediate vicinity of
other devices or on top of each other, and if it is required to operate it in the immediate vicinity of other devices or
as well as
on top of each other, it is necessary to monitor the examination light.
ranty is
xcluding
Table 1: Environmental emission limits (according to IEC60601-1-2).
Table 1: Environmental emission limits (according to IEC60601-1-2).
act your
Conducted and radiated emissions
or
Distortion due to high-order harmonics
Voltage fluctuations and flicker
a) For information on categories of environments for intended use, see p. 8.9
b) These tests do not apply to this environment, unless the ME-DEVICES (medical electrical devices) and ME-SYSTEMS (medical electrical systems) used in it are
connected to a public mains supply and their power consumption fluctuates in a range that is within the application range of the cited EMC basic standard.
c) ME-DEVICES AND ME-SYSTEMS designed for use in aircraft must comply with the emission requirements according to ISO 7137. Measurement of conducted
emissions is required only when the corresponding ME-DEVICES AND ME-SYSTEMS are designed to be connected to the aircraft on-board network. The ISO 7137
standard is identical to the RTCA DO-130C:1989 and EU-ROCAE ED-14C:1989 specifications. The latest editions of these specifications are RTCA DO-160G:2010 and
EUROCAE ED-14G:2011. For this reason, Section 21 (and Category M) of a later edition, e.g., [39] or [40], should be considered.
d) For other relevant operating conditions or other electromagnetic environments during transportation, the appropriate standards shall apply if they provide for the
proper use of ME-DEVICES and ME-SYSTEMS. Examples of possible suitable standards include CISPR 25 and ISO 7637-2.
36
Phenomenon
Class B, Group 1 (according to CISPR 11)
See IEC 61000-3-2
See IEC 61000-3-3
Professional health care institutions
b)
b)
Home health environment
CISPR 11 c),d)
See IEC 61000-3-2
See IEC 61000-3-3