Please note technical specifications may vary upon the manufacturer's discretion!
The surgical aspirator is intended for use in the electromagnetic environment specified below.
The customers or the user of the surgical aspirator should assure that it's used in such an environment.
Emissions Test
Power disturbance
CISPR11
Irradiated / Conducted emissions CISPR11
Harmonic emissions IEC/EN 61000-3-2
Voltage fluctuations / flicker emissions
IEC/EN 61000-3-3
The surgical aspirator is intended for use in the electromagnetic environment specified below.
The customers or the user of the surgical aspirator should assure that it's used in such an environment.
Immunity Test
Electrostatic discharge (ESD)
~
Hz
I
O
Guidance and manufacturer's declaration – Electromagnetic Emissions
Guidance and manufacturer's declaration – Electromagnetic Immunity
Room humidity percentage:
SYMBOLS
Class II isolation equipment
CE marking in conformity with EC directive 93/42/EEC and subsequent
Manufactured by: CA-MI Srl – Via Ugo La Malfa nr.31
43010 Pilastro (PR) Italia
Warning, consult the instruction manual
Keep in a cool, dry place
Conservation temperature: -40 ÷ 70°C
DEHP Phthalates (Suction catheter)
Compliance
Group 1
Class [B]
Class [A]
Complies
Compliance
± 6kV on contact
9
10 ÷ 100% RH
changes
Type B equipment
Fuse
Alternate Current
Mains Frequency
ON
OFF
Electromagnetic environment - guidance
The surgical aspirator 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 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.
Electromagnetic environments - guidance
Floors should be wood, conceret or ceramic