OPTIMedical OPTI CCA-TS User manual

OPTI™CCA-TS Analyzer
Operator’s Manual

OPERATOR’S MANUAL REVISION LOG
(Please record any changes made to this manual)
Proprietary Rights Notice
Information in this document is subject to change without notice. Companies, names and data used in examples
are fictitious unless otherwise noted. No part of this document may be reproduced or transmitted in any form
or by any means, electronic, mechanical or otherwise, for any purpose, without the express written permission
of OPTI Medical Systems, Inc. OPTI Medical Systems, Inc. may have patents or pending patent applications,
trademarks, copyrights or other intellectual or industrial property rights covering this document or subject matter in
this document. The furnishing of this document does not give a license to these property rights except as expressly
provided in any written license agreement from OPTI Medical Systems.
© 2016 OPTI Medical Systems, Inc. All rights reserved.
OPTI, the OPTI Medical logo, and ComfortSampler are trademarks or registered trademarks of OPTI Medical
Systems, Inc. in the United States and/or other countries. Other trademarks are the property of their respective
owners.
Made in U.S.A.
OPTI Medical Systems, Inc.
235 Hembree Park Drive
Roswell, GA 30076 USA
www.optimedical.com
PD7040 REV I
Revision Release Date Approved by Description
A Sept 2004 Released per CO 040316
B Oct 2004 Per CO 040329
C July 2005 Per CO 050197
D April 2006 Per CO 060151
E June 2007 Per CO 070249
F Sept 2007 Per CO 070338
G Dec 2010 Per PCR 100339
H Jan 2011 Per PCR 110016
H 15OCT13 1003
I 08JUN16 Per CO 1770
REP
EC Emergo Europe
Molenstraat 15
2513 BH, The Hague
The Netherlands

Important Information! Important Information!
This Operator´s Manual contains important warnings and safety information to be observed
by the user.
This instrument is only intended for one area of application which is described in the
instructions. The most important prerequisites for application, operation and safety are
explained to ensure smooth operation. No warranty or liability claims will be covered
if the instrument is applied in areas other than those described or if the necessary
prerequisites and safety measures are not observed.
The instrument is only to be operated by quali f ed personnel capable of observing these
prerequisites.
Only accessories and supplies either delivered by or approved by OPTI Medical Systems
are to be used with the instrument.
Due to this instrument’s operating principle, analytical accuracy not only depends on
correct operation and function, but also upon a variety of external inf uences beyond the
manufacturer’s control. Therefore, the test results from this instrument must be carefully
examined by an expert, before further measures are taken based on the analytical
results.
Treatment should never be administered based on results that are f agged on the
printout.
Instrument adjustment and maintenance with removed covers and connected power
mains are to be performed only by a qualif ed technician who is aware of the dangers
involved.
Instrument repairs are to be performed only by the manufacturer or qualif ed service
personnel.
Important Information! Important Information!

Operating Safety Information
Operating Safety Information
 Overvoltage Category II when connected to a branch circuit.
 This equipment has been tested and found to comply with the limits for a Class A digital
device, pursuant to Part 15 of the FCC Rules.
Caution:
 The instrument is designed as a conventional device (closed, not waterproof type).
 Do not operate the instrument in an explosive environment or in the vicinity of explosive
anesthetic mixtures containing oxygen or nitrous oxide.
 This instrument is suitable for continuous operation.
 The power plug is to be plugged into a ground socket only. When using an extension cord,
make sure that it is of the proper size and is properly grounded.
 Any breakage of the ground lead inside or outside the instrument or a loose ground
connection can cause a hazardous condition when operating the instrument. Intentional
disconnection of the grounding is not permitted.
 When replacing the fuses, make sure that they are of the same type and rating as the
original fuses. Never use repaired fuses or short-circuit the fuse holders.
This device is a Class 1 Laser product according to the requirements of IEC 60825-1.
The maximum energy output is as follows:
670 nm (LED): 40 Microwatts max. for 400ms
780 nm (Laser): 40 Microwatts max. for 400ms
850 nm (Laser): 40 Microwatts max. for 400ms
Caution: Use of controls or adjustments or performance of procedures other than those
specif ed herein may result in hazardous radiation exposure.

Symbol Definitions
The symbols described below are used on the packaging of OPTI™CCA-TS related products.
Symbol Explanation
Attention Symbol – Refer to the Operator’s Manual or Service Manual
for further instructions. This symbol is located on the inside of the
instruments and product packaging.
Expiration / Use By Symbol – Product to be used by the expiration
date indicated to the right of this symbol. This symbol is located on all
consumables, which are controlled via an expiration or use by date.
Batch Code Symbol – Manufacturing lot number is located to the
right of this symbol. This symbol is located on all products, which are
controlled via a lot number.
Do Not Re-use Symbol – Identifies products which are not to be
used for more than the specified period of time as defined in the
product instructions. This symbol is located on all applicable product
packaging.
Recycle Plastic Symbol - Identifies the clear plastic material
(polyethylene terephthalate glycol) used in the packaging of the
product. Containers identified with this symbol can be considered
recyclable. This symbol is located on all applicable product packaging.
WEEE-Symbol - This product complies with WEEE Directive
2002/96/EC which mandates the treatment, recovery and recycling of
electric and electronic equipment.
EXP
LOT

Symbol Explanation
Biohazard Symbol – Products and/or components containing this symbol
should be handled as biohazardous material after use.
Temperature Limit Symbol – Products and/or components which contain
this symbol must be stored within the specified temperature range.
For in-vitro diagnostic use
This product fulfils the requirements of Directive 98/79/EC on in-vitro
diagnostic medical devices.
Catalog number
Please read pack insert. / Follow the instrument’s instructions for use!
Manufactured by
Authorized European Community Representative
REF
C
F
C
F
EC REP

PREFACE
Welcome
Your OPTI™CCA-TS Analyzer is a powerful tool designed to help you quickly, accurately
and efficiently conduct basic testing of hydrogen ion concentration (pH), carbon dioxide partial
pressure (PCO2), oxygen partial pressure (PO2), sodium (Na+), potassium (K+), ionized calcium
(Ca++), chloride (Cl-), glucose (Glu), blood urea nitrogen (BUN), lactate (Lac), total hemoglobin
concentration (tHb) and hemoglobin oxygen saturation (SO2), depending on the cassette
configuration, in the convenience of your own laboratory.
This manual will help guide you through setting up your analyzer and will help you start
analyzing samples. As you become familiar with the operation of the unit, you should use the
manual as a reference for day-to-day routines and as a guide for maintenance and troubleshooting.
How to use this manual
If you have an analyzer that is not yet set up, you should begin by reading Chapters 1 and 2.
For programming and quality control functions, read Chapters 3 and 4.
Information on analyzer operation and maintenance is contained in Chapters 5 and 6.
Detailed service information and operating principles can be found in Chapters 7 and 8.
PREFACE