MEMBRANE SUCTION-IRRIGATION PUMP
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not be used in the vicinity of combustible gases.
•Themanufacturerisresponsibleforthesafety,reliabilityandperformanceofthesystemonlyif:
- Assembly, expansions, new settings, changes and repairs are carried out by authorized persons.
- Electrical installation of the operating room corresponds to the national standards for medical institutions.
- The device is used in compliance with the operating instructions and with its associated accessories.
- The device was switched on with all connecting elements fully connected and the system accessories
were checked for operability before every use.
•Weacceptnoresponsibilityorliabilityfordamageofanykindduetomisuse,abuse,violationofoperatinginstructions,
omission of required maintenance, equipment modications and service by unauthorized persons! Use of other than
originalaccessoriesshallvoidwarrantyandliability!
•Equipotentialbondingpinistobeusedtogetanadditionalpotentialequalizationforthepatient.PleaseconsiderEMC
notes.
The device complies EMC standards DIN EN 60601-1-2 Ausgabe 2007. Nevertheless, EMC interference may lead to
malfunction. If malfunction is observed, ensure that the device has been installed and is operated in accordance with the
EMCguidelines.Notethatportableandmobilehighfrequencycommunicationequipmentmayinuencetheoperation
of this device. If the device is used in the vicinity of or stacked together with other devices, the device or system must
be monitored to ensure standard operation in accordance with these guidelines. If necessary, refer to manufacturer for
further details.
WARNING! The application of pump for small and closed body cavities (arthroscopy and hysteroscopy) is strictly forbidden,
because irrigation process may lead to uncontrolled and dangerous pressure rise.
CAUTION! To avoid risk of electric shock device must be connected to public mains with protective earth conductor only.
IMPORTANT! In case of failure switch off the device by its main power switch. Defective device or parts are to dispose to
the national standards. When operating lifetime has expired manufacturer will take back device for recycling.
description and description description
Follow the instructions for use Type BF applied part Year of production
Legal manufacturer
mdcmedicaldevicecerticationGmbH,
Kriegerstraße 6,
70191 Stuttgart, Germany
Equipotential
(equalising potential)
C a u t i o n!
Hazardous voltage Batch number Article number
Expiring date Non-sterile, reusable Protective earthing
Product contains phthalate Sterilized with ethylene oxide Footswitch connector
Do not re-use Do not use if package is
damaged
Spray protection (protection
against vertically falling drops)
Thisproductshouldbeusedonlybyqualiedmedicalprofessionals!
Notexplosionproof.Donotusethedevicewithindemarcatedhazardzones(explosiveGases)!
Beforeopeningthecoverdisconnectmainsplug!
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