Contraindications; Technical Characteristics - Ca-Mi AS-36BR Mode D'emploi

Table des Matières

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Using the device in environmental conditions different than those indicated in this manual may harm seriously the safety

and the technical characteristics of the same.

10.

The medical device is in contact with the patient by means of a disposable probe (not supplied with the device). Suction

tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993-1 standards

on material biocompatibility.

11.

The product and its parts are biocompatible in accordance with the requirements of regulation EN 60601-1.

12.

Operation of the device is very simple and therefore no further explanations are required other than those indicated in the

following user manual.

13.

The lead battery integrated in the device is not to be considered as an ordinary domestic waste. Such a component must be

disposed of in a specific collection centre in order to be recycled.

14.

Use in Home-Care: Keep all accessories of the device out of reach of children under 36 months of age since they contain

small parts that may be swallowed.

15.

Do not leave the device unattended in places accessible to children and/or persons not in full possession of mental faculties

as they may strangle themselves with the patient's tube and/or the power cable.

Before using the AS-36BR, consult the instructions for use: failure to read all the instructions in this manual can be harmful

for the patient.

Don't use the device thoracic drainage.

The device must not be used for suction of explosive, corrosive or easily flammable liquids.

AS-36BR is not suitable for MRI. Do not introduce the device in MRI environments.

The manufacturer 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.

Any minimal modification / repair on the device voids the warranty and does not guarantee the compliance

with the technical requirements provided by the MDD 93/42/EEC (and subsequent changes) and its

IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC

DIRECTIVE 2012/19/UE-WEEE:

The symbol on the device indicates the separated collection of electric and electronic equipment. At the end of

life of the device, don't dispose it as mixed solid municipal waste, but dispose it referring to a specific

collection centre located in your area or returning it to the distributor, when buying a new device of the

sample type to be used with the same functions.This procedure of separated collection of electric and

electronic devices is carried out forecasting a European environmental policy aiming at safeguarding,

protecting and improving environment quality, as well as avoiding potential effects on human health due to the presence of

hazardous substances in such equipment or to an improper use of the same or of parts of the same Caution: The wrong disposal of

electric and electronic equipment may involve sanctions.

Model

Typology (MDD 93/42/EEC)

UNI EN ISO 10079-1 Classification

Power Feeding

Current Consumption

Maximum Suction Pressure (without jar)

Minimum Suction Pressure (without jar)

Maximum Suction Flow (without jar)

Weight

Insulation Class (when used with the AC/DC adapter mod.

UE60-140429SPA1)

Insulation Class (when used with an Internal battery)

Insulation Class (when used with a car cigarette lighter cable)

Size

Battery Holding Time

Battery Time Charge

Accurancy of Vacuum Indicator

Working Condition

Conservation condition and Transport