Instructions for Use
Electrosurgical Unit Minicutter
Revision 08 45
11 Guidelines and Manufacturer’s Declaration Regarding
Electromagnetic Compatibility (EMC)
Regarding EMC, medical electrical devices are subject to special safety measures, and they must be
installed and operated according to the EMC regulations laid out in this document.
Use of this device directly next to or stacked upon other devices should be avoided, as this could result in
faulty operation. If use as described above is still required, this
device and the other devices should be
monitored closely to ensure that they operate properly and safely.
Use of non-approved accessories and cables
Use of accessories or cables other than those specified or provided by the manufacturer of this device
may result in increased electromagnetic interference emission or reduced electromagnetic interference
immunity of the device, and in faulty operation. In case of doubt, contact Gebrüder Martin.
Guidance and manufacturer’s declaration – Electromagnetic emission
The electrosurgical unit Minicutter is intended for use in an electromagnetic environment as specified below. The
user must ensure that it is used in such an environment.
Electromagnetic interference
check
Compliance level Electromagnetic environment – Guidance
HF emissions according to
CISPR 11
Group 2
The device uses electromagnetic energy exclusively
for the performance of its internal functions. This may
cause interference in nearby electronic equipment.
HF emissions according to
CISPR 11
Class B
The limits of this class are kept only in standby mode
(without RF current activation)!
Harmonic emissions according to
IEC 61000-3-2
Class A
The device 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.
Voltage fluctuations/flicker
emissions according to
IEC 61000-3-3
Complies
To Next Page
Loading...
