Ca-Mi AS-36BR Mode D'emploi page 20

Using FLOVAC® disposable collection system: Before connecting the disposable collection system, remove the blu ring fitted
on the tank holder for a more comfortable insertion of the same container.
After opening the package, fully stretch the bag and then flatten it concentrically to eliminate as much air as possible.
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Insert the bag and apply the cover to an appropriately sized reusable rigid container by pressing firmly around the entire
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perimeter. Make sure that the system is completely sealed.
close the connector marked as "TANDEM" with the lid provided.
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Connect the power source of the vacuum to the VACUUM port equipped with specific reusable conical fitting with "male"
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connection.
Connect the patient tube to the PATIENT port of the cover
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Before use, check all closures and make sure there are no leaks, starting the aspiration source. If the bag expands to fully
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adhere to the walls of the rigid container and the cover bends towards the inside of the glass, the system is not leaking.
Start the aspiration and periodically check the filling level of the container. The overflow valve will cause the interruption
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of aspiration if the aspirated fluids have reached the maximum filling level of the device.
When the float valve intervenes signalling the device is too full, the suction source must be disconnected within no more
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than 5 minutes.
Warning: The accidental inversion of connections may cause contamination for the operator and/or for the vacuum
generation equipment.
RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REMEDIES
This section contains information regarding the conformity of the compliance with the EN 60601-1-2 Standard.
The AS-36 BR surgical aspirator is an electro-medical device that requires particular precautions regarding electro-magnetic
compatibility and which must be installed and commissioned according to the electro-magnetic compatibility information
supplied. Portable and mobile radio communication devices (mobile phones, transceivers, etc.) may interfere with the medical
device and should not be used in close proximity with, adjacent to or on top of the medical device. If such use is necessary and
unavoidable, special precautions should be taken so that the electro-medical device functions properly in its intended operating
configuration (for example, constantly and visually checking for the absence of anomalies or malfunctions).
The use of accessories, transducers and cables different to those specified, with the exception of transducers and cables sold by
the appliance and system manufacturer as spare parts, can lead to an increase in emissions or in a decrease of the immunity of
the device or system. The following tables supply information regarding the EMC (Electromagnetic Compatibility)
characteristics of the electro-medical device.
The surgical aspirator AS-36 BR is intended for use in the electromagnetic environment specified below.
The customers or the user of the surgical aspirator AS-36 BR should assure that it's used in such an environment.
Emissions test
Irradiated / Conducted emissions
CISPR11
Irradiated / Conducted emissions CISPR11
Harmonic emissions EN 61000-3-2
Voltage fluctuations / flicker emissions
EN 61000-3-3
NEVER USE THE DEVICE WITHOUT JAR AND / OR PROTECTION FILTER
Guidance and manufacturer's declaration – electromagnetic Emissions
Compliance
Group 1
Class [B]
Class [A]
Complies
Electromagnetic environment - guidance
The surgical aspirator AS-36 BR 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 AS-36 BR 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.
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GB