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Vista
™
basic Instructions for Use 1/25
950787 Rev H 02/03
The CE mark confirms compliance
with the “Council Directive on
Medical Products 93/42/EEC”
dated the 14
th
of June, 1993.
B. Braun Melsungen AG
RESPONSIBILITY OF
MANUFACTURER
Manufacturer, assembly, and
installation personnel or instructors
can only be held responsible for any
effects on device safety, reliability,
and performance if
♦ Installation, expansion work,
readjustments, modifications, or
repairs are carried out by
personnel authorized by the
above,
♦ The electrical wiring for AC power
satisfies the requirements of VDE
0100, 0107, and/or the IEC
publications, or regional and/or
national variations,
♦ The device is operated in line with
the Instructions for Use, and
♦ Regular technical inspections
(Preventative Maintenance) are
carried out every 2 years as
outlined in the Service Manual.
INSPECTION ON DELIVERY
Despite careful packaging, the risk
of transport damage cannot be
entirely excluded. Upon delivery,
please check that nothing is
missing. Do not use a damaged
device! If the device is damaged,
contact the Service Department.
See “Maintenance, Storage, &
Service.”
Packaging: The pump packaging is
reusable.
Package Contents: Vista basic
Infusion Pump, drop sensor, power
cable, pole clamp, Instructions for
Use.