EKF Diagnostics Biosen C-Line GP+ User Manual

Important Information
User Manual Biosen C_line Clinic / GP+
5
The device is not approved for use in areas where there
is a risk of explosion.
Only use the Biosen device for the purpose described in
section 2 on page 6. Observe the specifications for the use, storage and
transport of products.
Only use equipment and consumables, which are
expressly approved for use with the Biosen device.
The device should be subject to yearly inspections and
servicing. It is recommended to make a service contract. Repairs to the
device must only be performed by EKF-diagnostic GmbH or an
authorised service partner. For further maintenance instructions refer to
section 12, page 44.
The device has parts that can move unexpectedly during
normal operation. The occurring forces are designed to exclude any risk
of injury. In addition, the device has a mechanism which immediately
stops the appropriate component when blocked. Nevertheless, it is
recommended not to touch these parts during operation because the
device may immediately abort a running measurement operation.
1.2 Abbreviations
STD Standard
C1 / C2 Control 1 and 2
STAT Urgent sample
G Glucose
L Lactate
QC Quality control
IFCC International Federation of Clinical Chemistry and
Laboratory Medicine
Hct Hematocrit

EKF Diagnostics Biosen C-Line GP+ Specifications

General

Brand	EKF Diagnostics
Model	Biosen C-Line GP+
Category	Measuring Instruments
Language	English