The CE mark confirms compliance with the “Council Directive on Medical Products 93/42/EEC” dated the 14th 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.”
Vista™ basic Instructions for Use 950787 Rev H 02/03
Packaging: The pump packaging is reusable.
Package Contents: Vista basic Infusion Pump, drop sensor, power cable, pole clamp, Instructions for Use.
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