Olympus KV-6 Gebrauchsanweisung
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Specification
Classification
Standards compliance
Complies with EN ISO 10079-1 and EN IEC 60601-1 and UL 60601-1
(electromedical
Electro-magnetic
This product complies with the requirements of EN IEC 60601-1-2 for emissions and immunity, and as such, its operation is unlikely to
equipment)
Compatibility
be affected by, or cause interference with, equipment meeting appropriate EMC standards. As a precaution, equipment which may be
sensitive to interference outside the limits specified by EN IEC 60601-1-2 should not be placed in close proximity to the KV-6.
Type of protection against
Classification according to EN IEC 60601-1 / UL 60601-1: Class 1 with Type CF applied part.
electrical shock
Degree of protection
In accordance with EN IEC 60601-1 and UL 60601-1, the KV-6 is marked with the symbol to indicate the provision of an adequate
against electrical shock
degree of protection against electrical shock and that it has an applied part isolated from all other parts of the equipment.
Degree of protection
None: the Olympus KV-6 must NOT be used in the zone of risk of flammable anaesthetic gases.
against explosion
Mode of operation
Continuous
Regulatory status
European Economic Area
CE This mark on the product indicates compliance with Directive 93/42/EEC relating to medical devices, Class IIa.
(EEA)
Dimensions and weight Dimensions
Height: 210mm
Weight
9.3 kg
Power switch
Marking
The power switch is marked . A white LED in the center signalizes it is turned on
Power requirements
Power supply
100-240 V~
Fusing
Frequency
50/60Hz
Power rating
Environmental
Ambient Temperature
Operational:
+5ºC to +40ºC (+41ºF to +104ºF)
conditions
Storage:
-20ºC to +50ºC (-4ºF to +122ºF)
Relative humidity
Operational:
30-75 %
Storage:
20-95%
Atmospheric pressure
Operational/Storage:
70.0 to 106 kPa
Fluid Ingress
In accordance with EN IEC 60601-1/UL 60601-1, the product is marked IP21 to indicate that it is provided with an enclosure that prevents entry of such an amount of
falling liquid as might interfere with its safe and satisfactory operation when correctly positioned.
Resistance to
The external surfaces of the Olympus KV-6 are resistant to: 2% aqueous neutral detergent, 70% ethyl alcohol, isopropyl alcohol, water.
chemicals
Pump specification
Nominal vacuum: 95 kPa
Nominal free air flow rate: 50 l/min, adjustable to 40 or 60 l/min.
In accordance with ISO 10079-1, the unit is marked with the words 'HIGH VACUUM, HIGH FLOW' to indicate it has a vacuum of at least 60 kPa in 10 seconds and a
free air flow rate of 20l/min or greater.
Thermal cut-out
The temperature is observed by a sensor in the housing. If the temperature in the housing exceeds 80 °C (176 °F), the software stops the motor and turns on the yellow
LED. It is possible to restart the motor again as soon as the temperature in the housing drops below 70 °C (158 °F).
Single use suction liner To prevent fluid from being drawn up to the pump the single use suction liner contains a mechanism to shut off the flow when the liner is overfilled. This mechanism is
activated when contact is made with aspirated fluid.
Suction jar
The suction jars can be autoclaved up to 135 ºC or disinfected. The jar is impact resistant.
Suction jar lid
The suction jar lid clips and where applicable the float mechanism, are autoclavable up to 135 ºC. The inlet connection (from the endoscope) is marked with the word
PATIENT, the outlet connection (to the pump) is marked with the word VACUUM.
Tubing
Use only tubing specified in the KV-6 Instructions for Use, otherwise equipment malfunction may result.
Vacuum gauge
Range: 0 to 100 kPa
Accuracy: ±2.5%
OLYMPUS KEYMED
KeyMed House, Stock Road, Southend-on-Sea,
Essex SS2 5QH, United Kingdom
Telephone: +44 (0)1702 616333 Fax: +44 (0)1702 465677
e-mail: [email protected] www.keymed.co.uk
Width: 305mm
Depth: 375mm
2 x T1.6 AH
Marking: The mark ~ on
the product indicates the
120 W
requirement for an AC
power supply
For a complete listing of
sales and distribution locations visit:
www.olympus.com
Printed in UK PL022/201505
SUCTION PUMP
KV-6