HEINE ML4 LED Mode D'emploi page 6

Procedure
Clean and disinfect the DV1 manually (wipe clean and wipe disinfect).
Recommended agents:
Cleaning agent: Neodisher MediClean
®
Disinfection agent: quaternary ammonia compounds (e.g. Microbac
Conditioning residues on optics may be removed using a low-bacterial, dry,
micro-fibre cloth.
Please follow the cleaning notes for the ML4 in the identically named
instructions for use.
Maintenance and Service
The instruments do not require maintenance or service.
General Warnings
Check the correct operation of the device before use! Do not use the
device if there are visible signs of damage.
Do not use the device in fire- or explosive risk area (e.g. oxygen saturated
or anesthetic environments)
Do not modify the device.
Use only original HEINE parts, spare parts, accessories and power
sources.
Repairs shall only be carried out by qualified persons.
Route the supply cable in such a way that nobody can trip over it.
General Notes
The warranty for the entire product is invalidated if non-genuine HEINE
products or non-original parts are used and if repairs or modifications
are made to the device by persons not authorized by HEINE. For more
information, please visit www.heine.com.
Store and use the device in dry and dust-free environments only!
Disposal
The product must be recycled as separated electrical and electronic
devices. Please observe the relevant state-specific disposal regulations.
Electromagnetic Compatibility
Medical electric devices are subject to special precautionary measures with
regard to electromagnetic compatibility (EMC). Portable and mobile high
frequency communication equipment can affect medical electric devices.
This is a device in the domestic environment, this device may cause radio
interference, so that it may be necessary in this case, to take appropriate
remedial measures, as e.g. orientation, new arrangement or shielding of
the device or restrict the connection to the site.
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 device may not be stacked directly near or used directly beside other
devices. If the 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 following tables:
- Gudiance and Manufacturer's declaration - Electromangetic immunity
- Technical specification
- Explanation of the used symbols
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®
med 2714 2014-12-15