KaVo ORTHOPANTOMOGAPH OP 2D, Service Manual

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4 ORTHOPANTOMOGAPH OP 2D
1. General Information
1.4 Unauthorized Modi fi cations
Unauthorized changes or modi fi cations to any part of
the unit or its equipment can have hazardous conse-
quences. Changes or modi fi cations must not be made
unless speci fi cally authorized by the manufacturer of
the unit.
When properly assembled with a compatible beam-lim-
iting unit, the diagnostic source assembly will fully meet
the United States of America Federal Performance
Standards for Diagnostic X-Ray Systems and Their
Components (21 CFR 1020. 30-32) provided no compo-
nents or parts are removed from the unit and no unau-
thorized adjustments are made to the beam-limiting unit
or tube housing assembly.
Never remove or remanufacture any part of the tube
housing assembly or beam-limiting unit.
Never adjust any part of the beam-limiting unit unless
under the direction of the manufacturer of the unit or
their authorized distributor(s).
1.5 Disclaimer
The manufacturer of the unit shall have no liability for
consequential damages, personal injury, loss, damage
or expense directly or indirectly arising from the use of
its products. No agent, distributor or other party is au-
thorized to make any warranty or other liability on behalf
of the manufacturer of the unit with respect to its prod-
ucts.