HemoCue Albumin 201, Operating Manual

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Manufacturer
HemoCue AB
Box 1204
262 23 Ängelholm, Sweden
Telephone: + 46 77 570 02 10
Fax: + 46 77 570 02 12
Email: info@hemocue.se
www.hemocue.com
HemoCue Distributor USA
HemoCue America
250 South Kraemer Boulevard
Brea, CA, 92821
Phone(General): 800-881-1611
Orders: 800-323-1674
Technical Support: 800-426-7256
Fax (Cust. Service): 800-333-7034
www.hemocue.com
Warning
The device is tested according to standard IEC 60601-1
and IEC 60601 and is found to comply with the standard.
Despite this compliance it is impossible to predict any
possible effects by other near by standing instruments
or the possible impact of electromagnetic radiance. This
is the reason we need to inform users of this analyzer
that disturbance from other equipment might affect the
performance of the analyzer. Should you note that this is
the fact, please contact HemoCue America.
The HemoCue Albumin 201 system is intended for use in
the electromagnetic environment specified in Technical
specifications. The customer or user of the HemoCue
Albumin 201 system should assure that it is used in such
an environment. The HemoCue Albumin 201 system uses
RF energy only for its internal function. Therefore, its RF
emissions are very low and not likely to cause any inter-
ference in nearby electronic equipment.
The HemoCue Albumin 201 system is suitable for use in
all establishments, including domestic establishments
and those directly connected to the public low-voltage
power supply network that supplies buildings used for
domestic purposes.
Accessories connected to analog and digital ports must
be certified according to IEC 60601-1. All configurations
must comply to the IEC 60601-1-1. Further connection
to in or output are considered ”configuring a medical
system”, and must comply with IEC 60601-1-1.
For further information, please see Technical Specifica-
tions or contact HemoCue America.