8/40
med 1914 2014-08-08
Service
This product does not require regular service.
Disposal
The product must be recycled as separated electrical and electronic devices. Please observe the relevant
state-specific disposal regulations.
General Notes
Check the correct operation of the product at regular intervals. Do not use the equipment if it shows visible
signs of damage.
This product is a precise device. Please handle this product with care and store it in a clean place.
This product is not allowed to be entered or used in strong magnetic fields like MRI scanners.
We can only guarantee the performance of this instrument when fitted and used with original HEINE
accessories and spare parts. Otherwise the HEINE Warranty is terminated.
We can only guarantee the safety and performance of this unit if it is fitted with original HEINE accessories
and spare parts.
When moving from a cold to a warm environment, leave the power source switched off for up to one hour to
allow it to adapt to the new conditions.
The device must not be use or stored outdoors to prevent operational failures.
Safety Information
The medical electrical equipment may only be used by qualified medical personnel.
Do not expose the Li-ion mPack battery to ambient temperatures above +45°C.
All repairs should be carried out by qualified personnel, with the exception of a battery change with mPack.
When changing the battery, use only the original rechargeable battery HEINE
®
Li-ion mPack.
Do not use the device in rooms where an explosion hazard is present.
Electromagnetic Compatibility
Medical electric devices are subject to special precautionary measures with regard to electromagnetic compati-
bility (EMC). Portable and mobile high frequency communication equipment can affect medical electric devices.
This device is intended for use by medical professionals in the electromagnetic environment specified below.
The user of this device should assure that it is used in such an environment.
The use of accessories, converters or cables other than the ones specified by HEINE might lead to
increased emission reduced electrical immunity of the medical equipment.
The ME device may not be stacked directly near or used directly beside other devices. If the ME device is to
be operated in a stack or with other devices, the device should be watched to ensure it operates properly in
this location.
The appendix contains the tables „Guidance and Manufacturer’s declaration – Electromagnetic immunity“,
technical data and an explanation of the used symbols.