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Micromotors

MCX LED & MCX fig. 1a fig. 1b

Instruction
REF 2100231-0003/2014.05/ENG 0120

English Permanent
1.25 A rms
Medical devices entirely made in Switzerland
by Bien-Air Dental SA. I max.
5 A rms [10s]
Identification
Brushless electric micromotor. The most commonly Cooling
used coupling in the world as per ISO Standard Through compressed air from the unit. Place the fig. 2 fig. 3
3964. Sterilisables motors. flowmeter on the connector and set 10 to normliter/
Description MCX LED min. fig. 2. 0 1 2
With internal spray and light with LED light. Wash Disinfect Sterilization
Description MCX Air consumption output
With internal spray without light. 10 Nl/min.

USA Caution: Federal law restricts this device to sale Dimensions


by or on the order of a dentist. Ø 21 x 64 mm (0.82 x 2.51 inches) including the fig. 4 fig. 5 fig. 6
nose attachment.
Intended use Warning
Coupling Do not lubricate!!!
or Spray internally!!!
Product intended for professional use only. Use in Nose in accordance with ISO 3964, with internal
dentistry for prophylaxis, general dentistry and en- spray and light.
dodontics work.
The device is not designed for use in an explosive Weight
atmosphere (anaesthetic gas). 76 g (2.68 oz) without the cable.
The device is intended for medical treatment only; fig. 7 fig. 8
any use other than that for which this product is in- Operating times
tended is unauthorised and may be dangerous. The According to the type of electronics used.
medical device meets all the current legal require- • Do not clean in a washer-disinfectant impregnated with a detergent or disinfectant solu-
ments. Noise level unit fig. 8. tion fig. 5.
In accordance with ISO 11498, less than 53 dBA at • Only use original Bien-Air Dental maintenance
Technical data 45 cm (17.72 in). products and parts or those recommended by The motor must be rinsed as follows fig. 4
Bien-Air Dental. Using other products or parts • Hold the motor by the nose under running
Classification Recommanded rotation speed may cause operational failure and/or void the water (< 25ºC) as shown in the diagram below
Class IIa in accordance with European Directive From 1.000 to 40.000 rpm. guarantee. • Avoid allowing water to enter internally into the
93/42/EEC concerning medical devices. This med- motor either by the the nose or hose connector.
ical device is in compliance with the legislation in Direction of rotation In the event of prolonged disuse, the instrument Suitable detergents
force. Clockwise and anticlockwise. must be stored in a dry environment. Clean and • Detergent or detergent-disinfectant (pH 6- 9.5)
sterilise the instrument before reuse. recommended for cleaning-disinfection of den-
Electrical safety Torque tal or surgical instruments.
According to IEC 60601-1 standard (General safety Depending on the type of electronic controller used. Precautions of use • Quaternary ammonium- and/or enzyme-based
for Medical Electrical Equipement), the device shall The standard precautions in particular wearing surfactants.
be classified as a class II type B device. Associated Light MCX LED individual protection equipment (gloves, • Do not use solutions that are corrosive or con-
terminology is defined in sections 3.14 (3.13 if Class LED, variable from 10 klux to 38 klux. glasses…), must be complied with by healthcare tain chlorine, acetone aldehydes or bleaches.
I) & 3.132 of the same standard. The following personnel working with contaminated or potentially • Do not soak in physiological liquid (NaCl).
requirements as specified in IEC 60601-1 apply: Assembly contaminated medical instruments. Pointed and
• Protection against electrical shock sharp instruments should be handled with great 2 Sterilisation
• Ingress of liquids Important caution.
• Protection against excessive temperatures and Never connect an instrument on a running Do not use a sterilisation procedure other than the
other safety hazards micromotor. Check that the steriliser and the water that is used one described below.
are clean. After each sterilisation cycle, remove the
Electromagnetic compatibility Changing the seals, fig. 3 device from the sterilising apparatus immediately, Procedure: Fractionated pre-vacuum steam ster-
Corresponds to the electromagnetic compatibility in order to reduce the risk of corrosion. ilisation, Class B cycle acc. to EN13060. The proce-
in accordance with IEC 60601-1-2. Declaration by Disposal dure has been validated according to ISO 17664. All
the manufacturer regarding electromagnetic com- We recommend that the motor is cleaned and Bien-Air Dental straight handpieces are sterilisable
patibility. This device must to be recycled. Electrical and sterilised as described below before the initial in an autoclave up to 135°C (273.2°F). Duration:
electronic equipment may contain dangerous first use and subsequently after each treat- 3 or 18 min., depending to the national require-
Hose Junction fig. 1 substances which constitute health and environ- ment. ments in force.
Hose with connector type MCX. mental hazards. The user must return the device
Brushless type, 3-phase. Effective power according to to its dealer or establish direct contact with an 0 Cleaning Important
the type of electronic power supply used. approved body for treatment and recovery of this The quality of the sterilisation depends very much
Synchronous motor with permanent magnets. type of equipment (European Directive 2002/ The external surface of the motor must be cleaned on the cleanliness of the device. Only perfectly clean
Body of chromium and nickel-plated brass. Stain- 96/EC). to remove impurities as follows fig. 4. devices may be sterilised fig. 6.
less steel nose. • Hold the motor by the nose under running The instrument will function in excess of 500 ster-
Maintenance water (< 25ºC) as shown in the diagram below ilisations.
Rphase • With the aid of a soft bristled brush, clean the
0.9 Ohm Important external surface of the motor. 3 Lubrication
(included hose MCX resistance). • The instrument is delivered "non sterile". • Avoid allowing water to enter internally into the
• Before using for the first time and within a motor either by the the nose or hose connector. Important
Lphase maximum of 30 minutes after each treatment, The Bien-Air Dental micromotors MCX LED
60 μH clean, disinfect the attachment, then sterilise. 1 Disinfection and MCX are maintenance free.
Observing this procedure eliminates any blood,
Torque constant saliva or saline solution residues. Carefully rub the external surfaces of the motor, for Do not spray any lubricant or cleaning solu-
5.20 mNm/ A rms • Do not immerse in an ultrasonic bath. approximately one minute, with a soft bristle brush tion into the motor fig. 7!
REF 2100231-0003/2014.05/ENG 1/2
Servicing Rest the device on a suitable support to avoid risks The guarantee shall become null and void if the REF Legend
Never disassemble the device. For all modification of infection for yourself, the patient or third parties. damage and its consequences are due to improper
and repair, we recommend that you contact your manipulation of the product, or modifications to 1600751-001 Micromotor MCX LED, with
regular supplier or Bien-Air Dental directly. • To ensure the lifetime of the instrument , it is the product carried out by persons not authorised internal spray and LED
Bien-Air Dental asks the user to have its dynamic essential to maintain the quality of the cooling by Bien-Air Dental. 1600780-001 Micromotor MCX, with internal
instruments checked or inspected at least once a air and water utilised. spray without light
year. Claims under the terms of the guarantee will be 1600756-001 MCX hose, grey silicone
The compressed air should be dry and purified and considered only on presentation, together with the 1600756-0 MCX hose, special length
Transportation and storage conditions the compressor should be regularly maintained. product, of the invoice or the consignment note, on 1600824-001 B-MCX hose, grey silicone.
Temperature between -40°C (-40°F) and 70°C which the date of purchase, the product reference bayonet connection to unit
(158°F), relative humidity between 10% and 100%, To avoid the tubing and connectors from blocking, and the Serial No. should be clearly indicated. 1600824-0 B-MCX hose, special length
atmospheric pressure 50 kPa to 106 kPa (7.3 to the water should be filtered and purified to avoid 1300967-010 O-Ring for the motor MCX LED
15.3 psi). impurities and build-up of high levels of calcium and MCX
deposits. 1501566-001 Electronic DMCX
Information 1600307-001 Flow-meter for micromotors
The technical specifications, illustrations and Guarantee MCX LED and MCX
dimensions contained in these instructions are
given only as a guide. They may not be the subject Terms of guarantee Symbols
of any claim. The manufacturer reserves the right to Bien-Air Dental grants the operator a guarantee
make technical improvements to its equipment, covering all functional defects, material or produc- Manufacturer.
without amending these instructions. For all addi- tion faults. The device is covered by this guarantee
tional information, please contact Bien-Air Dental for 36 months from the date of invoicing. CE Marking with number of the notified
SA at the address indicated on the back cover. In the event of justified claim, Bien-Air Dental or its 0120 body.
authorised representative will fulfil the company’s
Other precautions for use obligations under this guarantee by repairing or Attention.
replacing the product free of charge. Any other
The device must be used by a qualified professional claims, of whatever nature, in particular in the form Light.
in compliance with the current legal provisions con- of a claim for damages and interest, are excluded.
cerning workplace safety, health and accident pre- Wear rubber gloves.
vention measures, and these working instructions. Bien-Air Dental shall not be held responsible for
In accordance with these requirements, the opera- damage or injury and the consequences thereof,
tors: resulting from: List of Bien-Air Dental SA registered Sterilisable at the specified temperature.
• must only use operating devices that are in per- • excessive wear and tear trade mark products ®:
fect working order; in the event of irregular • improper use Aquilon® Eolia® Lubrifluid® Prestilina® Recyclable electrical and electronic
functioning, excessive vibration, abnormal • non-observance of the instructions for installa- materials.
Bora® Gyro® Lubrimed® Spraynet®
heating or other signs indicating malfunction tion, operation and maintenance
of the device, the work must be stopped imme- • unusual chemical, electrical or electrolytic Boralina® Gyrolina® MX®
ChiroPro® Isolite® PowerCare® Electrical security.
diately; in this case, contact a repair centre that influences Applied part type B.
is approved by Bien-Air Dental; • poor connections, whether of the air, water or
• must ensure that the device is used only for the electricity supply. In these instructions, “Device” corresponds to the Move in the direction indicated.
purpose for which it is intended, must protect product described in the heading “Identification”.
themselves, their patients and third parties from The guarantee does not cover flexible “fibre optic” For example, turbine, contra-angle, handpiece,
any danger, and must avoid contamination type conductors, or any parts made of synthetic micromotor, tube, electronics, connectors, station Move fully to the stop, in the
through the use of the product. materials. etc. direction indicated.

Bien-Air Dental SA Bien-Air UK Ltd


This product may be covered by one or more of the following patents: Länggasse 60 Arundel House
EP Europe: 745358 / 688539 / 948294 / 1145688 / 1563800 / 1563801 / 1675523 / 1753360 DE Germany: 29616023.7 Case postale Unit 1 - Ground Floor
DK Denmark: 9600315 FR France: 2722972 CH Switzerland: 693922 CN China: 100528099 / 100522100 / 100522099 / 2500 Bienne 6, Switzerland Amberley Court, Whitworth Road
100553584 JP Japan: 3892485 / 4298933 / 7000419 US United-States: 5453008 / 6033220 / 6319003 / 7214060 / 7448870 Tel. +41 (0)32 344 64 64 Crawley, West Sussex,
RU Russia: 2361540 / 2361541 / 2372046 Fax +41 (0)32 344 64 91 RH11 7XL, England
office@bienair.com Telephone +44 (0)1293 550200
REF 1600751-001 MOT MCX LED / REF 1600780-001 MOT MCX Fax: +44 (0)1293 520481
Bien-Air ba-uk@bienair.com
Deutschland GmbH
Jechtinger Strasse 11 Bien-Air Asia Ltd.
Set supplied 79111 Freiburg, Deutschland Nishi-Ikebukuro
Tel. +49 (0)761 45 57 40 Daiichi-Seimei Bldg. 10F
MCX LED MCX Fax +49 (0)761 47 47 28 2-40-12 Ikebukuro, Toshimaku
ba-d@bienair.com Tokyo, 171-0014, Japan

Bien-Air España, SA
Entença, 169 Bajos
08029 Barcelona, España
Tel. +34 934 25 30 40 Tel. +81 (3) 5954-7661
Fax +34 934 23 98 60 Fax +81 (3) 5954-7660
ba-e@bienair.com ba-asia@bienair.com

Bien-Air USA, Inc. Beijing Bien-Air


Medical Technologies Medical Instrument
5 Corporate Park Technology Service Co. Ltd.
REF 1600751-001 REF 1300967-010 REF 1600780-001 REF 1300967-010 Suite 160 Room 907, The Exchange Beijing,
Irvine, CA 92606 USA No 118 Jian Guo Lu Yi,
Phone 1-800-433-BIEN Chao Yang District,
Optional accessories Phone 949-477-6050 Beijing 100022, China
Fax 949-477-6051
ba-usa@bienair.com

Bien-Air France Sàrl


55-57, avenue Jean Lolive
93508 Pantin Cedex, France Tel. +86 10 6567 0651
REF 1600824-001 Tel. +33 (0)1 41 83 60 70 Fax +86 10 6567 8047
REF 1600756-001
Fax +33 (0)1 48 96 07 40 ba-beijing@bienair.com
ba-f@bienair.com

Bien-Air Italia s.r.l.


Via Vaina 3
10x 20122 Milano, Italia
Tel. +39 (02) 58 32 12 51/52/54
Fax +39 (02) 58 32 12 53
REF 1300967-010 REF 1501566-001 REF 1600307-001 ba-i@bienair.com
REF 2100231-0003/2014.05/ENG 2/2

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