R-Biopharm RIDA QUICK SCAN II, Руководство пользователя

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General information
Please carefully compare the contents of this delivery with the enclosed delivery note, the
package leaflet or the invoice. We recommend that you keep a copy of this document
together with the instructions, so that you can quickly access information about the date
and scope of delivery in case of future queries, re-orders or service work.
Please be sure to remove all small parts from the packaging material. We like to inform you
that our devices are adjusted at the factory and can be used immediately after installation.
Before using the RIDA®QUICK SCAN II for the first time, please read the operating
instruction carefully. We recommend that it always be kept with the
RIDA®QUICK SCAN II.
Important information
The RIDA®QUICK SCAN II (item no. ZRQS2-KD) is an in vitro diagnostic medical device in
compliance with the German Medical Devices Act (§ 3 Paragraph 4 MPG) when operated
according to the manufacturer’s intended use for examining samples taken from the
human body.
According to the Regulations for Operators of Medical Devices (§2 Paragraph 5
MPBetreibV), users of medical products must ensure that these are functional and in good
condition. In addition, the user must observe the operating instructions as well as other
safety-related information and maintenance information.
The manufacturer of the in vitro diagnostic device is not responsible or liable for
information, evaluations, diagnoses, etc. that are obtained through the use of the in vitro
diagnostic device.