MEMBRANE SUCTION-IRRIGATION PUMP
Ackermann
Page: 6 // 20
not be used in the vicinity of combustible gases.
• The manufacturer is responsible for the safety, reliability and performance of the system only if:
- 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.
• We accept no responsibility or liability for damage of any kind due to misuse, abuse, violation of operating instructions,
omission of required maintenance, equipment modifications and service by unauthorized persons! Use of other than
original accessories shall void warranty and liability!
• Equipotential bonding pin is to be used to get an additional potential equalization for the patient. Please consider EMC
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
EMC guidelines. Note that portable and mobile highfrequency communication equipment may influence the operation
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.
Symbol and
description
Symbol
and description
Symbol and
description
Follow the instructions for use
Type BF applied part
Year of production
Legal manufacturer
mdc medical device certification GmbH,
Kriegerstraße 6,
70191 Stuttgart, Germany
Equipotential
(equalising potential)
Caution!
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)
This product should be used only by qualified medical professionals!
Not explosion proof. Do not use the device within demarcated hazard zones (explosive Gases)!
Before opening the cover disconnect mains plug!
0483
