Getting Started; Regulatory Considerations - tecan cavro xlp 6000 Operating Manual

1 Getting Started

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Cavro® XLP 6000 Modular Syringe Pump Operating Manual, 734237-C, en
Congratulations on your purchase of the Cavro® XLP 6000 Modular Syringe
Pump from Tecan Systems.
The XLP 6000 is a fully programmable, open frame, precision liquid handling
pump module, designed for applications in the 5 µL to 25 mL range. It is controlled
by an external computer or microprocessor and automates pipetting, diluting, and
dispensing functions.
This chapter includes these topics:

Regulatory Considerations

XLP 6000 Features at-a-Glance
Unpacking the XLP 6000
Functional Description of the XLP 6000
Safety
Tips for Setting Up the XLP 6000
Regulatory Considerations
The XLP 6000 is a general laboratory module. Since it not a medical device, it is
not subject to FDA regulatory approval. The XLP 6000 uses only recognized
components and bears the UL Recognized Component Mark:
The use of UL Recognized components in a product or system allows UL to focus
the evaluation of the complete system on its intended end-use, and thus speeds
up the evaluation of that product or system. For more information regarding UL
certification of Tecan Systems' syringe pumps, please visit the Underwriters
Laboratories Inc. website at http://www.ul.com/info/standard.htm. Tecan Systems'
customer file number for the recognized component is E164638.
CE
As a module designed for incorporation into larger systems that require
independent testing and certification, the XLP 6000 does not carry its own CE
mark.
1 - Getting Started
Regulatory Considerations
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