Model
Typology (MDD 93/42/EEC)
Classification UNI EN ISO 10079-1
Main Voltage
Power consuption
Fuse
Maximum suction aspiration (without jar)
Minimum suction aspiration (without jar)
Maximum flow (without jar)
Weight
Dimension
Functioning (to 35°C and 110 % operating voltage)
Working condition
Conservation condition
~
Hz
I
0
The surgical aspirator NEW ASKIR 30 is intended for use in the electromagnetic environment specified below.
Emissions test
Irradiated / Conducted emissions
CISPR11
Irradiated / Conducted emissions CISPR11
Harmonic emissions IEC/EN 61000-3-2
Voltage fluctuations / flicker emissions
IEC/EN 61000-3-3
TECHNICAL CHARACTERISTICS
Class 2 isolation equipment
CE marking in conformity with EC directive 93/42/CEE and subsequent changes
Manufacturer: CA-MI Srl - Via Ugo La Malfa n°31, 43010 Pilastro (PR) Italy
Warning, consult the instruction manual
Type B equipment
Fuse
Keep in a cool, dry place
Conservation temperature: - 40 ÷ 70° C
Alternate current
Mains frequency
ON
OFF
DEHP Phthalates (Suction catheter)
Guidance and manufacturer's declaration – electromagnetic Emissions
Compliance
Group 1
Class [B]
Class [A]
Complies
Medical Device Class II a
HIGH VACUUM / HIGH FLOW
Less -40kPa (- 0.40 bar)
NON-STOP OPERATED
Room temperature:
Room humidity percentage:
Altitude:
Room temperature:
Room humidity percentage:
SYMBOLS
Electromagnetic environment - guidance
The surgical aspirator NEW ASKIR 30 only used RF energy only for its
internal functioning. Therefore, its RF emissions are very low and are
not cause interference in proximity of any Electronic appliances.
The surgical aspirator NEW ASKIR 30 can be used in all environments,
including domestic and those connected directly to the public mains
distribution that supplies power to environments used for domestic
scopes.
9
NEW ASKIR 30
230 V ~ / 50 Hz
107 VA
F 1 x 1.6A 250 V
-80kPa (- 0.80 bar)
40 l/min
3.6 Kg
350 x 210 x 180 mm
5 ÷ 35 °C
30 ÷ 75 % RH
0 ÷ 2000m s.l.m
- 40 ÷70 °C
10 ÷ 100% RH