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CELL-DYN
®
3200 System Operator’s Manual
9140181K—July 2002
New CELL-DYN customer’s instruments are CE Marked to the European
In Vitro Diagnostic Directive, which encompasses the requirements of the
EMC and Safety Directives, and have the following labels:
Laser Label, Front Panel
Laser Label, Rear Panel
Serial Number Label, Rear Panel
CAUTION –
CLASS 3B LASER LIGHT WHEN OPEN.
AVOID EXPOSURE TO BEAM.
PN 9230701
CLASS 1 LASER PRODUCT
PN 9230702
ABBOTT DIAGNOSTICS DIVISION
Abbott Laboratories
Abbott Park IL, 60064 USA
THIS PRODUCT CONFORMS TO
THE APPLICABLE REQUIREMENTS
OF 21 CFR SUBCHAPTER J AT THE DATE
OF MANUFACTURE
DATE OF MANUFACTURE
MADE IN U.S.A. PN 9230308 REV G
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