Bedienungsanleitung Cami New Askir 30 (Seite 2 von 8) (Englisch)

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www.medicalsuction.co.uk

NEW ASKIR 30 12V Surgical aspirator is a portable unit, working with 12V dc (autotration battery), designed for the aspiration of bodily

fluids in adult and children. It’s particularly suitable for nasal, oral or tracheal aspiration of mucus, catarrh or blood after minor surgical

procedures and can be used in post-operative therapy at home or conveniently transported from one hospital ward to another.

The device is intended to be powered by a 12V DC car battery with non continuous operation (Ton: 20 min / Toff: 40 min)

Made of highly heat resistant, electrically insulated plastic material in conformity with the latest European safety standard, the product is

supplied with a complete polycarbonate autoclavable jar with overflow valve and it is equipped with aspiration regulator and vacuum

indicator located on the front panel.

GENERAL WARNING

READ INSTRUCTION MANUAL CAREFULLY BEFORE USE.

THE DEVICE IS FOR USE BY QUALIFIED PERSONNEL (SURGEON / PROFESSIONAL NURSE / ASSISTANT)

THE INSTRUMENT MUST NOT DISASSEMBLED. FOR TECHNICAL SERVICE ALWAYS CONTACT CA-MI SRL

IMPORTANT SAFETY RULES

1. Check the condition of the unit before each use. The surface of the unit should carefully inspected for visual damage. Check the

mains cable and do not connect to power if damage is apparent;

2. Before connecting the appliance always check that the electric data indicated on the data label and the type of plug used,

correspond to those of the mains electricity to witch it’s to be connected;

3. Respect the safety regulations indicated for electrical appliances and particularly:

- Use original components and accessories provided by the manufacturer to guarantee the highest efficiency and safety of the

device;

- The device can be used only with the bacteriological filter;

- Never immerge the appliance into water;

- Position the device on stable and flat surfaces in a way that the air inlets on the back aren’t obstructed;

- To avoid incidents, do not place the aspirator on unstable surfaces, which may cause it to accidentally fall and lead to a

malfunction and/or breakage. Should there be signs of damage to the plastic parts, which may expose inner parts of the energised

device, do not connect the plug to the electrical socket. Do not attempt to make the device work before it has been thoroughly

checked by qualified personnel and/or the CA-MI technical service department.

- Don’t use in the presence of inflammable substances such as anaesthetic, oxygen or nitrous oxide;

- Don’t touch the device with wet hands and always prevent the appliance coming into contact with liquids;

- Don’t leave the appliance connected to the power supply socket when not in use;

- Don’t pull the power supply cable to disconnect the plug remove the plug from the mains socket correctly;

- Store and use the device in places protected against the weather and far from any sources of heat. After each use, it is

recommended to store the device in its own box away from dust and sunlight.

- Don’t use the device thoracic drainage.

4. For repairs, exclusively contact technical service and request the use of original spare parts. Failure to comply with the above can

jeopardise the safety of the device;

5. Use only for the purpose intended. Don’t use for anything other than the use defined by the manufacturer. The manufacturer will

not be responsible for damage due to improper use or connection to an electrical system not complying with current regulation.

6. The medical device requires special precautions regarding electromagnetic compatibility and must be installed and used in

accordance with the information provided with the accompanying documents: the NEW ASKIR 30 12V device must be installed

and used away from mobile and portable RF communication devices (mobile phones, transceivers, etc.) that may interference

with the said device.

7. Instrument and accessory discharging must be done according to current regulations in the country of use.

8. WARNING: Do not change this equipment without the permission of the manufacturer CA-MI Srl. None of electric or mechanical

parts have been designed to be repaired by customers or end-users. Don’t open the device, do not mishandle the electric /

mechanical parts. Always contact technical assistance

9. 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 (supplied with the device) furnished with the

relative CE compliance certification according to the requirements of regulation ISO 10993-1: thus, no allergic reactions and skin

irritations may occur.

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.

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 normatives.

Cami New Askir 30 Seite 2

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