Abbott CELL-DYN 3200 System Operator's Manual page 3

Regulatory and Safety Agency Approvals
CELL-DYN 3200 System Operator's Manual
®
9140181K—July 2002
Abbott's liability for all matters arising from the supply, installation, use, repair,
and maintenance of the Instrument, whether arising under this Warranty or
otherwise, shall be limited solely to the repair or (at Abbott's sole discretion)
replacement of the Instrument or of components thereof. In no event shall Abbott
be liable for injuries sustained by third parties, incidental or consequential
damages, or lost profits. Replaced parts shall become the property of Abbott
Laboratories.
THE FOREGOING IS THE SOLE WARRANTY MADE BY ABBOTT
LABORATORIES REGARDING THE INSTRUMENT, AND ABBOTT
SPECIFICALLY DISCLAIMS ALL OTHER WARRANTIES, EXPRESSED OR
IMPLIED, INCLUDING THE IMPLIED WARRANTIES OF
MERCHANTABILITY AND OF FITNESS FOR A PARTICULAR PURPOSE.
The CELL-DYN 3200 Series Hematology Systems are manufactured by Abbott
Diagnostics, Abbott Laboratories, at 5440 Patrick Henry Drive, Santa Clara, CA
95054, U.S.A. Please direct all inquiries concerning information in this manual to
the foregoing address.
NOTE: Direct all inquiries regarding equipment problems to the Abbott
Hematology Customer Support Center. (U.S. customers only.)
In Vitro Diagnostic Directive
Legal Manufacturer
Authorized Representative
UL1262 Approved
CSA 22.2 # 151 Approved
IEC 1010-1 Approved
98/79/EC
Abbott Laboratories
Abbott Park, Il 60064 US
ABBOTT
Max-Planck-Ring 2
65205 Wiebaden
Delkenheim, Germany
iii