ED01_REV01-2020 IFU OB2012-2P_ENG
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Indicates that the user must consult these operating instructions for information, e.g. warnings
and precautions that may not be displayed on the medical device in question
CE marking in accordance with MDD 93/42/EEC for medical devices rated higher than class I
Manufacturer
Date of manufacture
Suction units OB 2012 contain electrical and/or electronic equipment that must be recycled in
compliance with European Directive 2012/19/UE - Waste Electrical and Electronic Equipment
(WEEE).
Authorized representative within the European Community if the manufacturer does not reside
in Europe
Expiry date
Order number (device code)
These operating instructions are available in other languages on the indicated website. Please
read them.
Do not use the device in environments where magnetic resonance imaging is performed
Production batch
Serial Number
Indicates that the suction unit is a medical device
Follow the operating instructions
Connection/patient suction tube (cover for collection jar and Serres® disposable liner)
INPUT
The accepted input voltage range is indicated on the external power supply inlet
OUTPUT
The output voltage is indicated on the external power supply outlet
Internal use only
Direct current
Alternating current
0.3. Symbols used on battery and referred to in these operating instructions
BATTERY
The battery is enclosed in a stiff plastic case and has a special internal electronic circuit to
prevent damage. The battery cannot be opened, disassembled or repaired
SLA
Sealed lead acid battery
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