General warnings
Failure to comply with these instructions may result in accidents involving serious personal injury:
The medical device manufacturer is responsible for the incorporation of a suitable safety
arrangement, if the actuator or lifting column is used for pull in an application where personal injury
can occur, which will prevent personal injury from occurring in case of actuator failure.
Note that during construction of applications, in which the actuator is to be fitted, there must be no
possibility of personal injury, for example the squeezing of fingers or arms.
The plastic parts in the system cannot tolerate cutting oil.
Assure free space for movement of the application in both directions to avoid a blockade.
The application and actuators are only to be operated by instructed personnel.
In applications with spline function, the blockage by an obstacle when the application is moving
inwards, the removal of the obstacle will cause the load to drop until the spindle hits the nut.
Do not turn the outer tube.
Do not use chemicals.
Inspect the actuator system regularly for damage and wear.
Do not expose LINAK actuator system components to high intensity ultraviolet radiation disinfection
lamps. This may damage the enclosure, supporting parts and cables.
LINAK actuators and electronics are not designed for use within the following fields:
• In the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide
• Planes and other aircrafts
• Explosive environments
• Nuclear power generation
If faults are observed, the products must be replaced.
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