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Leica M-series User Manual 54
•
The manufacturer assumes no respon-
sibility or liability for any use outside of
the intended use or use outside of the specifica-
tions from Leica Microsystems Wetzlar GmbH or
any risks resulting from such use.
In such cases, the Declaration of Conformity
shall be invalid.
•
This (IVD) device is not intended for use
in the patient environment defined by
DIN VDE 0100-710. It is also not intended to
be combined with medical devices as defined
by EN 60601-1. If a microscope is electrically
connected to a medical instrument in accor-
dance with EN 60601-1, the requirements
defined in EN 60601-1-1 shall apply.
General safety notes
This safety class 1 device was built and tested
in accordance with
EN 61010-2-101:2002
EN 61010-1:2001,
IEC 1010-1:2001,
Safety requirements for electrical equipment
for measurement, control and laboratory use.
The devices and accessories described in this
operating manual have been tested for safety
and potential hazards.
The responsible Leica affiliate or the main plant
in Wetzlar must be consulted whenever the
device is altered, modified or used in conjunc-
tion with non-Leica components that are
outside of the scope of this manual.
•
Unauthorized alterations to the instru-
ment or noncompliant use shall void all
rights to any warranty claims.
•
If any safety defects or malfunctions
of the Leica EL6000 are identified, the
instrument must be immediately disconnected
from the power system and secured against
additional use. For repair, the Leica EL6000
must be sent to the supplier or an authorized
representative of the supplier.
Leica EL6000 – Safety Notes