GE TONOPORT VI Operator's Manual page 12

Ambulatory blood pressure system
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Explanation of Signs and Symbols
Symbols used on the equipment and on the packaging
Follow the instructions given in the
operator manual.
This symbol indicates that the waste of
electrical and electronic equipment must
not be disposed as unsorted municipal
waste and must be collected separately.
Please contact an authorized
representative of the manufacturer for
information concerning the
decommissioning of your equipment.
Type BF applied part (defibrillation-
proof, recovery time t
Article number
Serial number
Lot number
UDI-DI
UDI-DI number
Medical device
CE marked per the Council Directive
0482
93/42/EEC of the European Union.
Notified body: MEDCERT GmbH.
Gossudarstwenny Standart Russia
(GOST)
Eurasian Conformity mark.
Conformity to applicable technical
regulations of Customs Union.
MEDICAL - PATIENT-
MONITORING EQUIPMENT AS TO
ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH ANSI/AAMI
ES60601-1 (2005) + AMD 1 (2012),
CAN/CSA-C22.2 No. 60601-1 (2014),
IEC 60601-1-6 (2010, A1:2013), IEC
60601-1-11 (2015), IEC 80601-2-30
(2009, A1:2013)
Caution: Federal law restricts this device
to sale by or on the order of a physician.
12
Controls and Indicators
< 1 s)
R
TONOPORT VI
Protection against ingress of solid
foreign objects and no protection against
IP20
ingress of water.
No protection against contact and
ingress of objects and protection against
IP02
dripping water when tilted at 15°.
Keep dry
Temperature limits
Humidity limits
Air pressure limits
USB port, connection to PC
Serial port, connection to PC
Manufacturer's identification
Date of manufacture.
The number found under this symbol is
the date of manufacture in the YYYY-
MM format.
Distributor's identification
Calibration mark, valid in Germany only
(see "Technical Inspections of the
Measuring System")
2001589-312 Revision B

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