SUCTION UNIT NEW ASPIRET USER MANUAL www.medicalsuction.co.
NEW ASPIRET Surgical Aspirator is a portable unit, working with 230V ~ / 50 Hz network electricity, 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. Easily portable equipment designed for continuous use.
IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC DIRECTIVE 2002/96/EC: In respect of art. 13 Decreto Legislativo 25 Luglio 2005, n.151 “Actuation of European directives 2002/95/EC, 2002/96/EC and 2003/108/EC, for reduction in use of dangerous substances in the electric and electronic device and for garbage disposal” The symbol as over applied on the device or its packaging means that at the end of its useful life the product must not be disposed of with domestic waste.
SYMBOLS Class II isolation equipment CE marking in conformity with EC directive 93/42/EEC and subsequent changes Warning, consult the instruction manual Keep in a cool, dry place Conservation temperature: -40 ÷ 70°C Type B equipment Fuse DEHP Phthalates (Suction catheter) ~ Hz I O Alternate Current Mains Frequency ON OFF Please note technical specifications may vary upon the manufacturer’s discretion! Guidance and manufacturer’s declaration – Electromagnetic Emissions The surgical aspirator NEW ASPIRET
Guidance and manufacturer’s declaration – Electromagnetic Immunity The surgical aspirator NEW ASPIRET is intended for use in the electromagnetic environment specified below. The customers or the user of the surgical aspirator NEW ASPIRET should assure that it’s used in such an environment. Immunity Test Compliance Electromagnetic environments guidance Electrostatic discharge (ESD) ± 6kV on contact Floors should be wood, concrete or IEC/EN 61000-4-2 ± 8kV in air ceramic tile.
CLEANING OF ACCESSORIES To clean the plastic housing of the device wear disposable latex gloves and clean with denaturated alcohol or hypoclorite solutions.
MAINTENANCE The NEW ASPIRET suction equipment does not need maintenance or lubrication. It is, however, necessary to inspect the unit before each use. Unpack the instrument and always check the plastic parts for any damage that may have occurred during prior use. Connect cable to electrical network and turn switch on. Close the aspiration outlet with your finger and with suction regulator at maximum check that the vacuum position reaches at least -75 kPa (-0.75 bar) maximum.
INSTRUCTIONS Place the unit on a flat, horizontal surface Connect the end of the short silicon tube, with antibacterial filter, to the suction connector. The other tube already connected to the filter has to be connected to the “VACUUM” jar outlet, where has been fixed the red float (security float). When the 90% of the volume of the jar is reached there is the activation of the security float (the float close the aspiration connector on the jar) to avoid liquid penetration inside the device.
Filter Assembling Mod: NEW ASPIRET FLOW DIRECTION IN / Fluid Inside Suction pump Inlet Jar Air Tube RULES FOR RETURNING AND REPAIRING COMPLYING WITH THE NEW EUROPEAN RULES, CA-MI INDICATES THE IMPORTANT POINTS TO PROTECT INSTRUMENT AND OPERATORS HYGIENE. THESE RULES MUST BE RESPECTED IN ORDER TO GUARANTEE HYGIENE AND SAFETY TO ALL THE PEOPLE OPERATING WITH THE INSTRUMENT TO OBTAIN QUALITY AND WELL BEING. CA-MI warrants it’s products for 24 months after purchasing date.
