Intended Purpose Of The Microscope - Leica DMI6000 B Operating Manual

2. Intended Purpose of the Microscope

2. Intended Purpose of the Microscope
The Leica DMI 6000 B microscope described in
these instructions is intended for biological rou-
tine and research applications. This includes the
examination of samples taken from the human
body to provide information on physiological or
pathological states or congenital abnormalities,
or determing the safety and compatibility with po-
tential recipients, or
measures.
The Leica DMI 6000 B is a further development
of Leica's proven inverted research micro-
scopes. It is designed for cellular and tissue ex-
amination, micromanipulation and microinjec-
tion techniques, microdissection, and confocal
microscopy. The Leica DMI 6000 B is suitable for
universal deployment, all contrast methods such
as darkfield, brightfield, phase contrast, DIC, flu-
orescence, and modulation contrast are integral
to the microscope and can be adapted or
changed quickly and easily. Variable illumination
and imaging beam paths, as well as HCS optics,
modular accessories and a comprehensive
range of peripherals, complement the Leica DMI
6000 B inverted research stand.
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monitoring therapeutic
The above-named microscope complies with
the Council Directive 98/79/EEC concerning in
vitro diagnostics. It also conforms to the Council
Directives 73/23/EEC concerning electrical ap-
paratus and 89/336/EEC concerning electromag-
netic compatibility for use in an industrial envi-
ronment.
Caution!
The manufacturer assumes no liability for
damage caused by, or any risks arising from
using the microscope for other purposes
than those for which it is intended or not us-
ing it within the specifications of Leica Mi-
crosystems Wetzlar GmbH.
In such cases the declaration of conformity
shall cease to be valid.
Caution!
This (IVD) device is not intended for use in
the patient environment defined by DIN VDE
0100-710. Neither is it intended for combin-
ing with medical instruments according to
EN 60601-1. If a microscope is electrically
connected to a medical instrument accord-
ing to EN 60601-1, the requirements de-
fined in EN 60601-1-1 shall apply.