Revision History (Continued) | xv
ELx800 Operator's Manual
Revision History (Continued)
P 10/06 Ch 3 Operation, clarified instructions for running Panel assays via the
keypad.
Ch 4 Instrument Qualification, replaced incorrect sample System Test
report with a report run using an ELx800.
Ch 5 Maintenance and Decontamination, added tips for storing and
handling filters.
Appx B, Using 384-Well Geometry, inserted step 13 to select a Read
Type when using Gen5.
Intended Use Statement
The intended use of this instrument is dependent on the instrument’s rear panel label.
If there is an IVD label, then the instrument may be used for clinical, research and
development, or other nonclinical purposes. If there is no such label, then the instrument
may only be used for research and development, or for other nonclinical purposes.
Quality Control
It is considered good laboratory practice to run laboratory samples according to
instructions and specific recommendations included in the assay package insert for the
test to be conducted. Failure to conduct Quality Control checks could result in erroneous
test data.
Repackaging and Shipping
If you need to ship the instrument to BioTek for service or
repair, contact BioTek for a Return Materials
Authorization (RMA) number, and be sure to use the
original packaging. Other forms of commercially available
packaging are not recommended and can void the
warranty. If the original packaging materials have been
damaged or lost, contact BioTek for replacement
packaging.
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