Risk Of Electromagnetic Interference And Possible Remedies - Ca-Mi MAT 130 Manual De Instrucciones

GB
1. PIace pump on a flat surface and hook it to the bed edge (foot side)
2. PIace the mattress on top of bed mattress with the 2 air connectors nearby the pump.
3. Connect the air hoses to the pump and mattress. The hose ending with connectors shall fit into the mattress.
4. Make sure the air hoses are not positioned or twisted underneath the mattress.
5. For operation, plug in the power cord, adjust the pressure with the knob and switch it on. The green light
indicates correct operation.
6. Allow 20 minutes for pad to inflate fully.
7. Cover with a sheet and tuck loosely.
8. Adjust the pressure for patient comfort.
The product has a 24-month warranty, valid from the date it is delivered by CA-MI S.r.l.
During the guarantee period free repair and / or replacement of any defective parts due to faulty manufacture will be
given, labour, postal, transport and packaging charges etc. are not included.
The guarantee therefore excludes components subject to wear and tear such as parts in rubber or PVC, etc.
Furthermore replacement or repairs effected during the guarantee period do not lengthen the duration of the guarantee.
This guarantee is void in the event of: repairs effected by unauthorised persons or with spare parts not approved
by CA-MI, damage or defects caused by negligence, blows, abnormal use of the appliance or faulty installation.
CA-MI S.r.l. cannot be held liable for accidental or indirect damages should the device be modified, repaired
without authorization or should any of its component be damaged due to accident or misuse.
The guarantee will be invalidated if the registration number has been removed, cancelled or altered.

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 device MAT-130 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.
Guidance and manufacturer's declaration – Electromagnetic Emissions
The device mod. MAT-130 is intended for use in the electromagnetic environment specified below. The customers or the
user of the device MAT-130 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
OPERATING INSTRUCTIONS
WARRANTY
Compliance
Group 1 The device MAT-130 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.
Class [B] The device MAT-130 can be used in all environments,
including domestic and those connected directly to the
public mains distribution that supplies power to
Class [A]
environments used for domestic scopes or hospital
Complies
12
Electromagnetic environment - guidance