IV
TECHNICAL SPECIFICATIONS
The control unit is mainly composed of the following elements:
•
1 x 12V-7Ah battery (back-up)
•
1 x transformer
•
2 x vacuum pumps: vacuum circuit (main pump + « back-up » pump)
•
valves for the vacuum & gas circuit
•
1 x gas regulator used for the set up of the nitrogen pressure going to the turbine (manual
microkeratomes)
•
Electronic boards.
Reference
mm
kg
Pressure
19380
430 x 240 x 190
13.6
IN : 4-6 bars / 58-87 psi
OUT : 2.5-3.5 bars / 36-50 psi
Precision of displayed values:
+/-0,2bar = 2,9 psi.
Vacuum display: +/- 30 mmHg
19381
Double footswitches:
2.55
220 x 200 x 60
Single footswitch :
100 x 70 x 30
19361
Double footswitches:
1.05
160 x 130 x 70
Single footswitch :
100 x 70 x 30
19381C
Double footswitches:
1.05
160X130X70
Simple pédale:
100X70X30
19381J
Double pédale:
2.55
220X200X30
Single footswitch:
100X70X30
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If a battery change is necessary, the used battery is classified as waste, which must be dealt with according to the specific regulations for
collection, treatment, recycling and disposal set out in directive 2006/66/EC of 9 September 2006 relating to batteries and accumulators and
waste batteries and accumulators. As such the battery must be disposed of at an appropriate collection point.
The Evolution 3E control unit and the electrical motors / turbines must follow the following conditions:
Temperature
Transportation
5 - 45°C / 41°F – 113°F
Storage
10 - 40°C / 50°F – 104°F
Normal conditions of use
10 - 40°C / 50°F – 104°F
All manuals and user guides at all-guides.com
Elect. Supply
100-120V / 220-240V
50/60Hz
Fuse : 500 mA high switching power
Battery :12 V - 7 Ah (Pb)
1
Power input: 50 VA
Humidity rate
Atmospheric
(without condensation)
pressure
30 - 90%
30 - 75%
30 - 75%
70 - 106 kPa
V.
REGULATORY INFORMATION
Electrical Safety Standard, electromagnetic
compatibility
Annexe "Guidance and manufacturer's
declaration: electromagnetic emissions and
immunity"
Customer Service Information
EUROPE
USA
VI. INTENDED USE
The power unit has been designed to operate Moria keratomes by means of electric motor or turbine.
Evolution 3E console must be used only by experienced ophthalmic surgeons with specific knowledge and
training in corneal surgery.
MORIA S.A.
15, rue Georges Besse - 92160 Antony - France
Phone +33 (0) 146 744 674
Fax +33 (0) 146 744 670
moria@moria-int.com
http://www.moria-surgical.com
IEC 60601-1
Classe I type BF
Refer to annexe document (#65073).
Contact your local dealer or MORIA.
0459
according to MDD 93/42/CEE
Product registered at the Food and Drug Administration (FDA).
Caution USA only: Federal law restricts the use of this device to
physicians or licensed practitioners.
For EU customers only: this symbol indicates that within the
European Union, the product must be discarded in a separate
collection bin at the end of its useful life. This applies not only to
this device, but also all accessories, including the footpedal and
electrical motors, regardless of whether those accessories are
marked with the symbol. Do not dispose as unsorted municipal
waste.
For users out of EU: please refer to local environmental regulatory
regarding waste of electrical and electronic equipment.
#65060/INTL-K-10.2020
MORIA
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