Drucker Diagnostics DASH COAG, Руководство оператора

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M
ODEL
D
ESCRIPTION
The DASH Coag centrifuge is engineered to reduce turnaround time (TAT) and simplify coag processing in the STAT
laboratory. Produce error-free samples in as little as 3 minutes with the DASH Coag’s simple set-and-lock controls,
preset cycle settings, and an LED lid lighting indicator system.
F
EATURES
o
Simple 2-Button interface
o
Three (3) easily selectable pre-set cycles are conveniently labeled for your lab’s most common applications. Use
the default cycles or customize them as needed. An LED light indicates the current selected setting.
o If desired, the control panel can be locked on one preset cycle for error-free reproducibility.
o Lid lighting indicates the centrifuge’s status (ready, running, done), keeping your TAT down (patent pending).
o A traditional audible alert indicates the completion of the cycle.
o
Cool–Flow air flow design prevents overheating of samples by maintaining room temperature.
o Carbon fibers are used to reinforce the tube holders and provide high strength and durability.
o A clear lid permits safe observation of samples and optical calibration of speed.
o The lid safety system only allows entry into the centrifuge after the rotor has completely stopped.
o The lid safety system prevents the centrifuge from operating unless the lid is closed and latched.
o The high power brushless DC motor provides years of operation with no routine maintenance.
I
NTENDED
U
SE
General purpose laboratory Centrifuge intended for safe and rapid density based separation of fluids, including
physiologic fluids, in approved specimen receptacles for qualitative or quantitative test procedures. As a general
purpose laboratory centrifuge, it is designed to also run other approved containers filled with chemicals (non-
flammable, non-explosive, non-volatile, and non-highly reactive only), environmental samples, and other non-
human body samples. This device is intended to be operated by properly trained personnel who have carefully read
the operating manual and are familiar with the function of the device.
[Refer to the clinical laboratory method specified by the specimen receptacle manufacturer or established by the
medical technology for the products applications.]