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Biolight Meditech S12 Vet - 3.1. Installation

Biolight Meditech S12 Vet
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S12 Vet Monitor User’s Manual
3-1
Chapter 3 Basic Operations
3.1. Installation
WARNING
The equipment should be installed by personnel designated by the
manufacturer.
The copyright of the software of this device belongs to the manufacturer. No
organization or individual can tamper with, copy or exchange any
infringement by any means or form without permission.
Equipment connected to the analog or digital interfaces must comply with the
respective IEC standards (e.g. IEC 60950 for data processing equipment and
IEC 60601-1 for medical equipment). Furthermore all configurations shall
comply with the current version of the standard for SYSTEMS IEC 60601-1.
Everybody who connects additional equipment to the signal input part or
signal output part configures a medical system, and is therefore responsible
that the system complies with current version of the requirements of the system
standard IEC 60601-1. If in doubt, consult the technical service department or
your local representative.
When the equipment is connected to other electrical equipment into a
combination with specific functions, if it is impossible to determine whether the
combination is dangerous (for example, the electric shock hazard caused by the
accumulation of leakage current), please contact the expert of the company or
the hospital to ensure that the necessary safety of all equipment will not be
damaged in the combination.
3.1.1. Unpacking and Checking
1. Unpacking
Before unpacking, examine the packing case carefully for signs of damage. If any
damage is detected, contact the carrier. If the packing case is intact, open the package.
2. Remove the monitor and accessories carefully.

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