Haemonetics PCS 2 User manual

0123
2
R
PCS
Printed in France
Haemonetics Corporation
400 Wood Road
Braintree, MA, 02184, USA P/N 85266-30, Manual revision: A
©2002, Haemonetics International. All rights reserved. April 2002
Working with the Haemonetics®PCS®2
- Operation Manual -

Preface iii
P/N 85266-30, Manual revision: A
CONSUMER INFORMATION
Proprietary rights The contents of this manual are property of the Haemonetics Corporation.
Haemonetics®and PCS®2 are registered trademarks of the Haemonetics Corpo-
ration. Any information or descriptions contained in this manual may not be
reproduced and released to any of the general public, or used in conjunction with
any professional instruction without written consent of Haemonetics Corpo-
ration, USA. Please direct any written inquiries to the appropriate address:
Legal disclaimer This manual is intended for use as a guide, uniquely for material as supplied by
the Haemonetics Corporation. It provides the operator with necessary informa-
tion to safely carry out specific procedures and satisfactorily maintain Haemo-
netics-produced equipment. The manual is to be used in conjunction with
instruction and training as supplied by qualified Haemonetics personnel.
Haemonetics guarantees its products when correctly used by a properly trained
operator. Any failure to respect the procedures as described could result in
impaired function of the equipment, as well as in injury to the operator and/or
patient /donor. Haemonetics accepts no responsibility for problems resulting
from failure to comply with prescriptions as outlined by the company. Any modi-
fications estimated as necessary by the customer should be evaluated by a
Haemonetics Clinical Specialist.
Safe utilization of Haemonetics material and equipment requires the operator to
correctly handle and dispose of blood-contaminated material. The operator of
any Haemonetics equipment must understand and implement the local policies
and standard operating procedures concerning the handling of blood-contami-
nated material, as well as blood products.
It remains solely the responsibility of the customer to fully assess and ensure the
safety of any products obtained from Haemonetics prescribed procedures, prior
to further application or use. Haemonetics declines any responsibility for choices
made by the consumer concerning the utilization of products and by-products.
In addition, it is the responsibility of the apheresis center using Haemonetics
equipment and material to inform the donor about the risks involved with any
apheresis procedure. Prior to initiating any procedure, the apheresis center is
responsible to verify that the donor understands these risks and consents to the
procedure.
International Headquarters
Haemonetics S.A.
Signy Center, P.O. Box 262
CH-1274 Signy 2 Switzerland
Tel. [phone]
Fax [phone]
Corporate Headquarters
Haemonetics Corporation
400 Wood Road
Braintree, MA, 02184, USA
Tel. [phone]
Fax [phone]

iv Preface
P/N 85266-30, Manual revision: A
Haemonetics
worldwide
locations
Haemonetics Asia Inc.
Taiwan Branch
26F-1, No. 102 Roosevelt Road Sec. 2
Taipei, Taiwan
Tel. [phone]
Fax [phone]
Haemonetics GesmbH
Handelsges.m.b.H.
Berlagasse 45/B2-02
A-1210 Wien, Austria
Tel. [phone]
Fax [phone]
Haemonetics Belgium NV
Leuvensesteenweg 542-BP. 14
Planet II Complex
B-1930 Zaventem, Belgium
Tel. [phone]
Fax [phone]
Haemonetics BV
C/O CITCO - WTC, PB 7241
Strawinskylaan 1725
1007 JE Amsterdam
The Netherlands
Tel. [phone]
Fax [phone]
Haemonetics Medical Devices
(Shanghai) International
Trading Co. Ltd.
Room 28032, Shanghai HSBC Tower
101 Yin Cheng East Road
Shangai 200120, PRC
Tel. [phone]
Fax [phone]
Haemonetics CZ, spol. S.r.o
Ptašínského C.8
60200 Brno, Czech Republic
Tel. [phone]
Fax [phone]
Haemonetics France S.A.R.L.
46 bis, rue Pierre Curie
Z.I. Les Gatines
F-78370 Plaisir, France
Tel. [phone]
Fax [phone]
Haemonetics GmbH
Rohrauerstrasse 72
D-81477 München, Germany
Tel. [phone]
Fax [phone]
Haemonetics Hong Kong Ltd.
Suite 1314, Two Pacific Place
88 Queensway, Hong Kong
Tel. [phone]
Fax [phone]
Haemonetics Italia S.R.L.
Via Donizetti, 30
20020 Lainate (MI), Italy
Tel. [phone]
Fax [phone]
Haemonetics Japan K.K.
Kyodo Building 3F
16, Ichiban-cho, Chiyoda-ku
Tokyo, Japan, 102-0082
Tel. [phone]
Fax [phone]
Haemonetics Scandinavia AB
Beta Huset, Ideon
Scheelegatan 17
S-223 70 Lund, Sweden
Tel. [phone]
Fax [phone]

Preface v
P/N 85266-30, Manual revision: A
Haemonetics (UK) Ltd.
Beechwood House
Beechwood Estate
Elmete Lane, Roundhay
Leeds LS8 2LQ, United Kingdom
Tel. [phone]
Fax [phone]
Haemonetics S.A.
Signy Centre
P. O . B o x 2 6 2
CH-1274 Signy 2, Switzerland
Tel. [phone]
Fax [phone]

P/N 85266-30, Manual revision: A
Table of Contents
Chapter 1 Explaining General Information
PROVIDING AN OVERVIEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is apheresis technology? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is the purpose of this manual? . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is the Haemonetics Plasma Collection System 2?. . . . . . . . . . . . . 1-3
What are the characteristics and features of the PCS2? . . . . . . . . . . . . . 1-3
What are the special features of the PCS2? . . . . . . . . . . . . . . . . . . . . . . 1-4
What is required to perform a procedure? . . . . . . . . . . . . . . . . . . . . . . . 1-4
UNDERSTANDING THE USE OF SYMBOLS . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found in this document. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found on the device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found on disposable packaging. . . . . . . . . . . . . . . . . . . . . . . . 1-8
LISTING DEVICE SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9
Chapter 2 Describing the PCS2 Device Components
PRESENTING THE PCS2 DEVICE COMPONENTS . . . . . . . . . . . . . . . . . . . 2-3
DESCRIBING THE CENTRIFUGE SYSTEM . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
System-sealing mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
Centrifuge well . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Centrifuge base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
DESCRIBING THE PCS2 CABINET COMPONENTS . . . . . . . . . . . . . . . . . . 2-7
Optical line Sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Weigher . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Pumps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Valves. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Donor flow lights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Air detectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Pressure monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Blood filter holder. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Solution-bag poles (2) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Power entry module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Power cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Pressure cuff . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Biohazard waste bag. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Communication box/data card (optional) . . . . . . . . . . . . . . . . . . . . . 2-16
Bar code reader (optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-16

viii Table of Contents
P/N 85266-30, Manual revision: A
DESCRIBING THE PCS2 CONTROL PANEL . . . . . . . . . . . . . . . . . . . . . . . 2-17
Display screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
Mode control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Protocol key. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Pump control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Programming keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Cuff key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
Valve control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
Chapter 3 Maintaining the PCS2 Equipment
CLEANING PROCEDURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Cabinet, control panel and valves . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Pressure monitors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Air detectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Optical sensors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Fluid detector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Centrifuge components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Pumps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Filter screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Barcode reader. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
CUSTOMER SERVICE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Clinical training . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Field service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Returned Goods Authorization system . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
HAEMONETICS®CLEANING AND MAINTENANCE RECORD . . . . . . . . . 3-8
Chapter 4 Ensuring Safety and Quality for a PCS2 Procedure
HANDLING THE PCS2 EQUIPMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Storing the PCS2 device and material. . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Inspecting the material. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
PREVENTING PROBLEMS DURING A PCS2 PROCEDURE. . . . . . . . . . . . . 4-3
Understanding the risk of hemolysis. . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Avoiding the consequences of flow restriction . . . . . . . . . . . . . . . . . . . 4-3
Avoiding bowl misalignment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Avoiding overheating due to mechanical situations . . . . . . . . . . . . . . . 4-4
Controlling for Red Cell Overrun . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
WARNINGS FOR THE OPERATOR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Electrical shock hazards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Leakage current control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Mechanical hazards/rotating parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Power outlet connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Communicable disease precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6

P/N 85266-30, Manual revision: A
Chapter 1
Explaining General Information
PROVIDING AN OVERVIEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is apheresis technology? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is the purpose of this manual? . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
What is the Haemonetics Plasma Collection System 2? . . . . . . . . . . . . 1-3
What are the characteristics and features of the PCS2? . . . . . . . . . . . . . 1-3
What are the special features of the PCS2? . . . . . . . . . . . . . . . . . . . . . . 1-4
What is required to perform a procedure?. . . . . . . . . . . . . . . . . . . . . . . 1-4
UNDERSTANDING THE USE OF SYMBOLS . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found in this document. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found on the device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Symbols found on disposable packaging . . . . . . . . . . . . . . . . . . . . . . . 1-8
LISTING DEVICE SPECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9

1-2 Explaining General Information
P/N 85266-30, Manual revision: A
PROVIDING AN OVERVIEW
What is apheresis
technology?
Apheresis is the general term used to describe the separation, selective removal
and collection of one or more of the individual components which together form
whole blood. This term can be subdivided into two categories:
zCytapheresis: selective removal of one or more of the formed, cellular
components of whole blood. These elements include erythrocytes,
thrombocytes and leukocytes.
zPlasmapheresis: selective removal of plasma, the liquid suspension me-
dium of blood. Plasma contains elements referred to as fractionable
components, such as clotting proteins and immunoglobulins.
Apheresis technology permits:
zThe collection and separation of whole blood.
zThe selective removal and collection of specific components.
zThe subsequent return of the non-selected components to the donor
or patient.
What is the
purpose of this
manual?
This manual is intended to supply anyone involved in using Haemonetics equip-
ment with the essential tool for safe and successful operation – information.
Using this tool of information, the operator can acquire knowledge to be applied
throughout all levels of operating experience. This body of information should be
consulted whenever necessary, starting from the initial contact with Haemonetics
technology to attain:
zAn awareness of the purpose of the device and the implications of its col-
lection procedures for the donor and the apheresis center.
zAn understanding of how to safely operate the Haemonetics system, cor-
rectly install the appropriate disposable material, and troubleshoot any
difficulties.
zAn ability to consistently apply the principles behind safe operation,
proper maintenance and correct handling to ensure optimal, quality
apheresis results.

Explaining General Information 1-3
P/N 85266-30, Manual revision: A
What is the
Haemonetics
Plasma
Collection
System 2?
Using updated apheresis technology, Haemonetics has produced the PCS2 - a
compact, lightweight plasmapheresis system which is as easy and safe to use as
it is technologically advanced.
The PCS2 automated apheresis technology provides the operator with a
maximum degree of flexibility in any type of plasmapheresis location. The
plasma collected may be designated for use in therapeutic transfusion. It may also
be conserved, used as source plasma and subsequently fractionated into plasma-
derived products.
What are the
characteristics
and features of
the PCS2?
The PCS2 is appropriately called a Plasma Collection System because it consists
of distinctive parts which collectively function as a whole system to produce a
designated final product:
zThe automated plasmapheresis device developed by Haemonetics
called the PCS2.
zThe process designed by Haemonetics to gather plasma from a donor
called a collection procedure.
zThe single-use collection material manufactured by Haemonetics called
a disposable set.
Once the operator has initiated a PCS2 procedure, plasma collection will
proceed automatically. The appropriate amount of anticoagulant solution will be
mixed in the disposable tubing with whole blood from the donor. This anticoag-
ulated blood will be drawn into a disposable collection bowl and separated by
centrifugal force into its various components.
When the bowl reaches its collection capacity, the plasma component will exit
the bowl and be directed into a plasma collection container for conservation.
Non-selected blood components will be returned to the donor. This cycle will be
repeated until the desired amount of plasma is collected.
The choice of the disposable collection material will depend on the desired
collection product. The PCS2 technology also provides the operator with the
option to infuse saline solution along with the blood components to the donor at
different points of a procedure, depending on the type of disposable bowl in use.
Haemonetics has designed the PCS2 technology with a degree of automation
which permits the operator to interact with the device. The operator should
remain attentive to the display screen messages while monitoring the status of the
donor. It is possible to modify certain aspects of the collection procedures, based
on the needs and requirements of the individual donor and the selected material.

1-4 Explaining General Information
P/N 85266-30, Manual revision: A
What are the
special features
of the PCS2?
Haemonetics has incorporated advanced technological features into the portable
PCS2 design. Examples of these features, which ensure safety for the donor and
permit efficient time-management for the operator, are:
zSelf-loading pumps.
zAdvanced optical sensors.
zDonor-line tubing pressure monitor.
zCommunication data box or internal data card.
zBarcode reader.
What is required
to perform a
procedure?
PCS2 collection procedures are quick and simple to perform. The following
material is required to perform a PCS2 procedure:
zA PCS2 disposable set designed for the selected procedure.
zVenipuncture materials and hemostats.
zAppropriate anticoagulant solution.
z0.9% normal saline (optional).
The operator will need to:
ÎInstall the appropriate disposable set.
ÎModify any settings if necessary.
ÎPerform a single venous puncture, prior to initiating a procedure.
Plasma collection will proceed automatically until the end-collection target has
been reached.

Explaining General Information 1-5
P/N 85266-30, Manual revision: A
UNDERSTANDING THE USE OF SYMBOLS
Symbols found in
this document
The terms note, caution and warning are used in this manual with the following
symbols to emphasize certain details for the operator.
Note: Provides useful information regarding a procedure or operating tech-
nique when using Haemonetics material.
Caution: Advises the operator against initiating an action or creating a situa-
tion which could result in damage to equipment, or impair the quality of the
by-products; personal injury is unlikely.
Warning: Advises the operator against initiating an action or creating a sit-
uation which could result in serious personal injury to either the donor or
the operator.
Symbols found on
the device
The descriptions of the following symbols are based on information provided in
the following documents:
zIEC Standard 60601-1, Medical Electrical Equipment,
Part 1: General requirements for safety.
zIEC Standard 60417-1, Graphical symbols for use on equipment,
Part 1: Overview and application.
Type BF applied part
This symbol indicates that the applied portion (i.e. the part which comes in
contact with the donor) of the device is electrically isolated. The device has
an internal electrical power source providing adequate protection against
electrical shock, in particular pertaining to acceptable leakage current and
the reliability of the protective earth connection.
Protective earth (ground)
Used to identify any terminal intended for connection to an external
conductor, for protection against electrical shock in case of a fault.

1-6 Explaining General Information
P/N 85266-30, Manual revision: A
~Alternating current
Used to indicate on the rating plate that the device is suitable for alternating
current only.
Fuse symbol
Used to identify fuse boxes or the location of a fuse box.
Power OFF
Position of the main power switch indicating disconnection from the mains.
Power ON
Position of the main power switch indicating connection to the mains.
IPX1 Protection against ingress of liquid
Indicates that the enclosure of the device is designed to provide a specified
degree of protection against harmful ingress of water or liquid into the equip-
ment (under applicable conditions).
Attention (Consult accompanying documents)
Non-ionizing electromagnetic radiation
Used to specify RF transmission for data communication.

Explaining General Information 1-7
P/N 85266-30, Manual revision: A
The following symbols have been designed for devices manufactured
by Haemonetics:
Bar-code reader connection
RS232 connection
RS232 connection with power to one pin
Pressure cuff connection

1-8 Explaining General Information
P/N 85266-30, Manual revision: A
Symbols found on
disposable
packaging
The following symbols are used by Haemonetics on disposable set packaging.
CATALOG NUMBER
EXPIRATION DATE
Lot Number
Sterilized by exposure to Ethylene Oxide
Fluid path STERILE by exposure to Ethylene Oxide
Sterilized by exposure to Gamma irradiation
Fluid path STERILE by exposure to Gamma irradiation
DO NOT REUSE
Caution: consult operator manual for instructions
Storage conditions, humidity level
Storage conditions, temperature level
REF
LOT
80%
8%

Explaining General Information 1-9
P/N 85266-30, Manual revision: A
LISTING DEVICE SPECIFICATIONS
The approximate weight and dimensions of the PCS2 device are as follows:
The following environmental conditions should be respected pertaining to oper-
ation and storage of the PCS2 device:
The electrical specifications for operating the PCS2 device are as follows:
Note: Haemonetics will regulate the proper voltage setting upon installation.
The power source used must be properly grounded.
Characteristics Values
Cabinet
cover open Cabinet cover closed
Height 63 cm 44 cm
Width 55 cm
Depth 55 cm 32 cm
Depth with communication box 55 cm 37 cm
Weight 26.4 kg
Weight with communication box 27.4 kg
Conditions Values
Ambient operating temperature +18°C to +27°C
Tested storage temperature 0°C to + 40°C
Storage humidity level Maximum relative humidity rate of 90%,
non-condensing
Characteristics Values
(relative to input voltage)
Input voltage 230 VAC ± 10% 110 VAC ± 10%
Operating current ~1.9 A ~ 2.6 A
Fuse rating F2.5 A @ 250 V F5.0 A @ 250 V
Operating frequency range 50 - 60 Hz 50 - 60 Hz
Maximum leakage current 500 µA 100 µA

1-10 Explaining General Information
P/N 85266-30, Manual revision: A
Caution: The PCS2 device must be operated in an environment compatible to the
requirements of the IEC 60601-1-2 Standard, Electromagnetic compatibility.
Mobile RF communication equipment not approved by Haemonetics and porta-
ble communication equipment can affect the PCS2 device. Any accessories and
cables not approved by Haemonetics used in conjunction with the device may
increase hazards and influence compatibility with EMC requirements. Therefore,
non-approved accessories and cables must not be used.
In addition, the PCS2 device and accessories must not be placed directly adja-
cent to, or top of other equipment, unless specifically approved by Haemonetics.

P/N 85266-30, Manual revision: A
Chapter 2
Describing the PCS2 Device Components
PRESENTING THE PCS2 DEVICE COMPONENTS. . . . . . . . . . . . . . . . . . . . 2-3
DESCRIBING THE CENTRIFUGE SYSTEM . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
System-sealing mechanism . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
Centrifuge well. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Centrifuge base. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
DESCRIBING THE PCS2 CABINET COMPONENTS. . . . . . . . . . . . . . . . . . . 2-7
Optical line Sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Weigher . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Pumps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Valves. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Donor flow lights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Air detectors. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Pressure monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Blood filter holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Solution-bag poles (2). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Power entry module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Power cord. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Pressure cuff. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Biohazard waste bag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Communication box/data card (optional) . . . . . . . . . . . . . . . . . . . . . . 2-16
Bar code reader (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-16
DESCRIBING THE PCS2 CONTROL PANEL . . . . . . . . . . . . . . . . . . . . . . . 2-17
Display screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
Mode control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Protocol key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Pump control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Programming keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Cuff key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
Valve control keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21

2-2 Describing the PCS2 Device Components
P/N 85266-30, Manual revision: A
Figure 2-1, PCS2 device components
19
20
9
24
23
22
21
25
12
14
17
13.
54
6
11
3
18
7
1
8
2
B
9
13
16
10
A
15
A. Cabinet
1. Centrifuge
2. Line sensor
3. Weigher
4. Anticoagulant (AC) pump
5. Blood pump
6. Donor valve (red)
7. Plasma valve (yellow)
8. Saline valve (white)
9. Donor flow lights (x2)
10. Anticoagulant line air de-
tector (ACAD)
11. Blood line air
detector (BLAD)
12. Donor line air detector 1
(DLAD1)
13. Donor line air detector 2
(DLAD2)
14. Blood filter holder
15. AC solution pole
16. Saline solution pole
17. Donor pressure monitor
(DPM)
18. System pressure monitor
(SPM)
B. Control Panel
19. Display screen
20. Mode control keys
21. Protocol key
22. Pump control keys
23. Programming keys
24. Cuff key
25. Valve control keys