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FOR USE IN DENTISTRY ONLY!
MM.CONTROL is a medical device in accordance with Medical Device Directive 93/42/EEC, amended by Directive
2007/47/EC.
MM.CONTROL is exclusively designed for use by dental practitioners for use with root canal preparation instruments.
MM.CONTROL is a micromotor with an integrated apex locator (for determining canal length). This device should only be
used in hospitals and dental clinics or practices by qualified dental professionals.
CONTRAINDICATIONS
The use of MM.CONTROL is contraindicated in patients or users with implanted electronic devices such as pacemakers,
etc. Do not use the device for other non-endodontic dental procedures.
WARNINGS
This chapter contains a description of severe adverse reactions and potential safety hazards for the product or the user/
patient. Please read the following warnings before use.
USE
MM.CONTROL is designed for use in the field of dentistry and should only be operated by trained, qualified professionals,
e.g. dentists.
ENVIRONMENTAL CONDITIONS
The device may cause interferences or disturb the functioning of nearby devices. If this happens, reduce spurious emis-
sions by reorienting or moving the MM.CONTROL.
MM.CONTROL is not suitable for use in damp areas or anywhere where the device may come into contact with any type
of liquids. Do not expose the device to any direct or indirect sources of heat. The device must be operated and stored in a
safe environment.
The device requires special safety precautions with regard to electromagnetic compatibility (EMC). The EMC information
provided in this manual must be strictly adhered to during installation and operation. It is especially important not to use
the device near fluorescent lamps, radio transmitters, remote controls and portable or mobile radio frequency communica-
tions equipment.
In order to avoid possible danger from electromagnetic interference, do not operate any other electrical medical device or
other devices near the MM.CONTROL. The electromagnetic radiation emitted by the device is below the recommended
limits set by the applicable regulations (EN 60601-1-2:2014).
The lip clip or file grip cables must not be pinched or pulled when plugging in or unplugging components. The cables
should not hinder the movement of people. The use of accessories other than those specified, with the exception of com-
ponents sold by the manufacturer as replacement parts, may result in increased emissions or decreased immunity of the
device.
POWER SUPPLY:
No mains operation.
BATTERY
If the battery LED light turns orange, recharge the battery. If the battery LED light turns red or flashing red, recharge the
battery as soon as possible to prevent the MM.CONTROL from shutting down. The MM.CONTROL may not be used when
it is charging.
If the MM.CONTROL battery leaks, remove the battery and replace it with a genuine MICRO-MEGA battery only.
During use: Dental dams and rubber gloves are recommended when using the MM.CONTROL.
Should an operating fault occur when using the device, switch the device off and contact MICRO-MEGA or the approved
technical support centre.
COMPONENTS AND ACCESSORIES
Only use the original white leads, lip clip and file grip supplied with the MM.CONTROL.
Only use endodontic instruments to determine the working length.
Please follow the manufacturer's instructions when using endodontic instruments. These are not supplied with the
MM.CONTROL.
MM.CONTROL may not be connected to, or used in combination with, other devices or systems. It may not be used as a
component for another device or system.
CARE AND TRANSPORTATION
MM.CONTROL components are not delivered disinfected or sterilised: components such as the central unit, lip clip, white
leads and file grip must be disinfected before the first use and after every additional use.
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