Equipo 01 ClinitekAdvantusLIS PDF

Clinitek AdvantusTM and Clinitek® 500 Analyzers
Interface Specification
04826807 Rev. A, 2008-05
04826807 Rev. A
© 2008 Siemens Medical Solutions Diagnostics. All rights reserved.
No part of this manual or the products it describes may be reproduced by any means or in
any form without prior consent in writing from Siemens Medical Solutions Diagnostics.
Clinitek Advantus, Clinitek, Multistix, Multistix PRO, N-Multistix, Uro-Hema-Combistix,
Uristix, Hema-Combistix, Labstix, N-Neostix, Uro-Uristix, Combistix and Clinitek
Microalbumin are trademarks of Siemens Medical Solutions Diagnostics.
Lantronix and XPort are trademarks of Lantronix.
Origin: Ireland (Clinitek 500), UK (Clinitek Advantus)
The information in this manual was correct at the time of printing. However, Siemens
Medical Solutions Diagnostics continues to improve products and reserves the right to
change specifications, equipment, and maintenance procedures at any time without notice.
If the system is used in a manner differently than specified by Siemens Medical Solutions
Diagnostics, the protection provided by the equipment may be impaired. See warning and
hazard statements.
Clinitek Advantus and Clinitek 500 Interface Specification 1
04826807 Rev. A
Contents
Using this Manual
How this Manual is Organized . . . . . . . . . . . . . . . . . . . . . 0-1
Conventions Used in this Manual . . . . . . . . . . . . . . . . . . 0-2
1General Specifications
Serial Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1
Clinitek 500 Serial Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-1
Clinitek Advantus Serial Port. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2
Clinitek Advantus Ethernet Port . . . . . . . . . . . . . . . . . . . . . . . . .1-3
2Data Flow
Transmission Specifications . . . . . . . . . . . . . . . . . . . . . . 2-1
Character Structure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1
Electrical Characteristics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1
Interface Connections. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
Signal Levels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
Speed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
Data Link Layer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
Data Characters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
Data Transfer Phases. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Establishment Phase (Link Connection) . . . . . . . . . . . . . . . . . . . . . .2-4
Transfer Phase . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Termination Phase (Link Release) . . . . . . . . . . . . . . . . . . . . . . . . . .2-7
Error Handling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7
Timeouts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Establishment Phase Timeouts. . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Transfer Phase Timeouts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Message Structure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Supported Record Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Communication Sessions. . . . . . . . . . . . . . . . . . . . . . . . 2-10
Request for Identification Communication Session . . . . . . . . .2-10
Standard ASTM Identification Request Session . . . . . . . . . . . . . . .2-10
Single Character Identification Request Session. . . . . . . . . . . . . . .2-12
Order Communication Session. . . . . . . . . . . . . . . . . . . . . . . . .2-14
Order Communication Session . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-14
Order Data Exchange . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-15
Results Reporting Communication Session. . . . . . . . . . . . . . .2-17
04826807 Rev. A
2 Clinitek Advantus Interface Specification
Results Communication Session . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
Results Data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-18
Results Data Exchange . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
3Formatting Test Records
Record Structure and Content . . . . . . . . . . . . . . . . . . . . .3-1
Restricted Characters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Message Header Record Format. . . . . . . . . . . . . . . . . . . . . . . .3-4
Example of a Message Header Record . . . . . . . . . . . . . . . . . . . . . . 3-6
Language/Result Unit Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Message Terminator Record Format . . . . . . . . . . . . . . . . . . . . .3-7
Examples of a Message Terminator Record . . . . . . . . . . . . . . . . . . 3-8
Request Information Record Format . . . . . . . . . . . . . . . . . . . . .3-8
Example of a Request Information Record. . . . . . . . . . . . . . . . . . . . 3-8
Order Record Format. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-9
Examples of Order Record. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Patient Record Format. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-10
Patient Record – Test Sequence Format. . . . . . . . . . . . . . . . . . . . 3-10
Example of the Patient Record – Test Sequence. . . . . . . . . . . . . . 3-10
Patient Record – Results Format . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Example of the Patient Record – Results Record . . . . . . . . . . . . . 3-11
Test Strip ID . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Error Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Result Record for Clinical Results Format . . . . . . . . . . . . . . . .3-14
Examples of Results Records. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-16
Test Strip Assays and Abbreviations . . . . . . . . . . . . . . . . . . . . . . . 3-16
Appendix A: Safety Instructions
Protecting Yourself from Biohazards. . . . . . . . . . . . . . . .A-1
References. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-2
Appendix B: Service, Ordering, and Warranty
Siemens Authorized Representative . . . . . . . . . . . . . . . .B-1
Limited Instrument Warranty and Service Delivery Policy. .B-1
Warranty Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-1
Additional Service Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-2
Service During Normal Hours. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-2
Extent of a Service Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-2
Service Outside Normal Hours. . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-2
Clinitek Advantus and Clinitek 500 Interface Specification 3
04826807 Rev. A
Replacement of Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2
Design Changes and Retrofitting of Instruments. . . . . . . . . . . . . . . B-3
Key Operator Designation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
OSHA Requirements (US only). . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
Warranty and Service Exclusions . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
Information for Technical Assistance . . . . . . . . . . . . . . . B-5
Locating the System Serial Number and Versions. . . . . . . . . . .B-5
Addresses. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-5
Appendix C: Result Unit Tables
English and Chinese Conventional Units. . . . . . . . . . . . . . . . . . . . . C-1
English and Chinese S.I. Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-5
English Nordic Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9
French Conventional Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-13
French S. I. Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-17
German Conventional Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-21
German S. I. Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-25
Italian Conventional Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-29
Italian S.I. Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-33
Japanese Conventional Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-37
Japanese JCCLS Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-41
Portuguese Conventional Units. . . . . . . . . . . . . . . . . . . . . . . . . . . C-45
Portuguese S.I. Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-49
Spanish Conventional Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-53
Spanish S.I. Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-57
Swedish Conventional Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-61
Swedish S.I. Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-65
Swedish Nordic Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-69
Appendix D: Clinitek 200/200+ Emulation Mode
Data Transfer Characteristics. . . . . . . . . . . . . . . . . . . . . . . . . . .D-1
Output Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-1
Output Data Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-2
Global Formatting for all Data Sets Output to Serial Port . . . . . . . . D-3
Calculation of Checksum. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3
Instrument ID Message (Serial Output Only) . . . . . . . . . . . . . . .D-5
Variable Field Definitions for Test Result Output . . . . . . . . . . . .D-7
CLINICAL Results Format Output . . . . . . . . . . . . . . . . . . . . . . .D-8
Global Formatting Requirements for all CLINICAL Mode Results. . D-8
Multistix“ Family of Test Strips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-9
Multistix PRO Family of Test Strips. . . . . . . . . . . . . . . . . . . . . . . . D-10
04826807 Rev. A
4 Clinitek Advantus Interface Specification
Result Value Conversions from Clinitek Advantus and Clinitek 500 to
Clinitek 200 . . . . . . . . . . . . . . . . . . . .D-12
Result Value Conversions from Clinitek Advantus and Clinitek 500 to
Clinitek 200+ . . . . . . . . . . . . . . . . . . .D-34
Appendix E: Glossary
04826807 Rev. A
Using this Manual

The Clinitek AdvantusTM and Clinitek® 500 Interface Specification is written primarily for
software developers who are familiar with implementing layered communications protocols.
This manual provides the interface specifications for connecting the Clinitek Advantus and
Clinitek 500 analyzers to your host computer or laboratory information system (LIS). The
manual provides information on the data string and formatting of clinical results generated using
the appropriate Clinitek reagent strips.
How this Manual is Organized
The following table provides an overview of the manual and explains the contents of each
section:
If you want to . . . Refer to . . .
review the specifications for the interface
connections,
Section 1, General Specifications
understand how the data is transmitted
between the analyzer and the computer or
LIS,
Section 2, Data Flow
learn about the test result formats and how
to set them up on your computer or LIS,
Section 3, Formatting Test Records
review biohazard guidelines, Appendix A, Safety Instructions
contact
Siemens Medical Solutions Diagnostics
Appendix B, Service, Ordering, and
Warranty
view result unit tables for all supported
languages,
Appendix C, Result Unit Tables
learn about the Clinitek 200/200+
emulation mode and how to set it up on
your computer or LIS,
Appendix D, Clinitek 200/200+
Emulation Mode
find a definition for an unfamiliar term, Appendix E, Glossary
2 Clinitek Advantus and Clinitek 500 Interface Specification: Using this Manual
04826807 Rev. A
Conventions Used in this Manual

The Clinitek Advantus and Clinitek 500 Interface Specification uses the following text and
symbol conventions:
Convention Description
Bold Bold type indicates the following:
• text on the user interface.
For example, if the word save appears as Save, it refers to
the Save button on the user interface.
• a key on the keyboard or a system key on the front of the
system.
For example, when the word enter appears as Enter, it
refers to the Enter key on the keyboard.
• the actual text of a message transmitted between the system
and an LIS.
the actual value stored in the database.
Italic Italic type refers to the title of a document or a section title in
this manual. For example, Overview of Layered
Communications Protocols refers to Section 2 of this manual.
CAUTION
Caution statements alert you to conditions that may cause
product damage or loss of data. On the system, this symbol
indicates that you should refer to the manuals for more
information.
NOTE: Note statements alert you to important information that requires
your attention.
04826807 Rev. A
1 General Specifications
The Clinitek Advantus and Clinitek 500 Urine Chemistry Analyzers can transmit data to a
computer or Laboratory Information System (LIS). The Clinitek Advantus analyzer can use
either a serial interface or an ethernet port.
Serial Interface
The following information details the serial interface for each analyzer:
•Clinitek 500 serial port
•Clinitek Advantus serial port
•Clinitek Advantus ethernet port
Clinitek® 500 Serial Port
The serial port on the Clinitek Advantus analyzer is a 25 pin D-Connector. This port allows
serial connectivity to an external computer or host.
Settings for the Clinitek 500 serial port are described in the following tables:
Table 1-1 Clinitek 500 Serial Interface Port Specifications
Specification Description
Voltage At receiver end (RD)
≥ +3 V is logic 0 (Space)
≥ −3 V is logic 1 (Mark)
At transmitter end (TD)
EIA-232-D 1986 Standard
Cable length maximum 15.2 m (50 ft)
Cable type null modem serial cable
Pins 2 and 3 are crossed, pins 4 and 5 are crossed, pins 6 and
20 are crossed, and pins 1, and 7 are straight through.
Data bit 8 bit with No Parity
7 bit with No Parity
7 bit with Even Parity
7 bit with Odd Parity
The default is 8 bit characters.
Handshake ON/OFF (for CT200/200+ emulation only)
Checksum ON/OFF (for CT200/200+ emulation only)
Baud rates 1200, 2400, 4800, 9600, 19200
The default is 9600
Parity NONE, EVEN, ODD
The default is NONE.
Stop Bit 1 (Binary 1)
1–2 Clinitek Advantus and Clinitek 500 Interface Specification: General Specifications
04826807 Rev. A
Table 1-2 Clinitek 500 Serial Port Connector RS232 25 Pin (DB25)
Clinitek AdvantusTM Serial Port
The serial port on the Clinitek Advantus analyzer is a 9 pin male D-Connector. This port allows
serial connectivity to an external computer or host. The settings for the serial port are
independent of those for the ethernet port.
Settings for the Clinitek Advantus serial port are described in the following tables:
Table 1-3 Clinitek Advantus Serial Interface Port Specifications
Pin Signal
1 Chassis ground
2 TXD
3 RXD
4 RTS
5 CTS
6 DSR
7 Signal ground
20 DTR
Specification Description
Voltage At receiver end (RD)
At transmitter end (TD)
EIA-232-D 1986 Standard
Cable length maximum 15.2 m (50 ft)
Cable type 9-pin null modem serial cable
Pins 2 and 3 are crossed, pins 4 and 6 are crossed, pins 7 and
8 are crossed, and pins 1, 5, and 9 are straight through.
Start bit 1 (Binary 0)
Data bit 8 bit with No Parity
7 bit with No Parity
7 bit with Even Parity
7 bit with Odd Parity
The default is 8 bit characters.
Handshake ON/OFF (for CT200/200+ emulation only)
Checksum ON/OFF (for CT200/200+ emulation only)
Baud rates 1200, 2400, 4800, 9600, 19200
The default is 9600
Parity NONE, EVEN, ODD
The default is NONE.
Stop Bit 1 (Binary 1)
Clinitek Advantus and Clinitek 500 Interface Specification: General Specifications 1–3
04826807 Rev. A
Table 1-4 Serial Port Connector RS232 9 Pin (DB9)
Clinitek Advantus Ethernet Port
The Clinitek Advantus analyzer has the ability to connect to a hospital LIS through an ethernet
port located at the rear of the instrument. This port offers a 10/100 base T connection using
TCP/IP protocols.
This connector is a Lantronix XPort 10/100mB Ethernet to RS232 port converter. Settings are
independent of those for the RS232 serial port.
The cabling required for the ethernet connector is as follows:
Table 1-5 Cabling Requirements
Table 1-6 Clinitek Advantus Ethernet Port Connector Twisted Pair, RJ45
Pin Signal
1 CD
2 RX
3 TX
4 DTR
5 Ground
6 DSR
7 RTS
8 CTS
9 RI (not used)
Connection Requirement
Instrument connecting to the network Standard straight through CAT5
Instrument connecting to the PC Standard crossover CAT5
Pin Signal
1 TD+ (or tpe 0)
2 TD- (or tpe 1)
3 RD+ (or tpe 2)
4 Common Mode Termination
6 RD- (or tpe 3)
1–4 Clinitek Advantus and Clinitek 500 Interface Specification: General Specifications
04826807 Rev. A
Port number: 10001
MAC address, 00-20-4A-XX-XX-XX, the first, second and third bytes are fixed (00-20-4A)
identifying the unit as a Lantronix product. The fourth, fifth and sixth bytes are unique numbers
assigned to each unit.
At the Setup menu, under network settings, you can enter either a static IP address or a DHCP
name.
The analyzer blocks the following IP addresses as Invalid:
•0.0.0.0
•255.255.255.255
•127.X.X.X.
The Internet Protocol and RFC-3300 assigned the following IP addresses as special use and you
should avoid using them:
•0.0.0.0/8 – This network broadcast address
•169.254.0.0/16 – Used by the DHCP protocol
•192.0.2.0/24 – Used for network testing
•192.88.99.0/24 – Used by IPv4 to IPv6 relay hosts
•192.18.0.0/15 – Used for host-to-host benchmarking
•224.0.0.0/4 – Used for multicasting
•240.0.0.0/4 – Reserved for use by IANA
In addition, avoid any address in which all bits outside the subnet mask are “1.” For example, if
the subnet mask is 255.255.255.0, and address of the form X.X.X.255. The RFC 950 defines
these as broadcast addresses that refer to every host on a local network so they should not be
assigned to an individual host.
Two bi-colored LEDs (light emitting diodes) are built into the port allowing the user to monitor
the port status.
Table 1-7 Port Status
Link LED – Left side Activity LED – Right side
This condition Means This condition Means
Off No link Off No activity
Amber 10Mbps Amber Half-duplex
Green 100Mpbs Green Full-duplex
04826807 Rev. A
2 Data Flow
The section contains the conventions used for the data exchanged between a host computer or
LIS and the Clinitek Advantus and Clinitek 500 analyzers.
NOTE:Some analyzer versions show Bayer in the record content. This a vestige of programming
and does not imply any connection or relationship between Bayer and Siemens.
Transmission Specifications
Transmission specifications include:
•Character structure
•Electrical characteristics
•Interface connections
•Signal levels
•Speed
Character Structure
The method of data transmission is serial-by-bit start/stop. The order of the bits in a character is:
1. One start bit, corresponding to a binary 0.
2. The data bits of the character, least significant bit being transmitted first.
3. Parity bit.
4. Stop bit(s), corresponding to a binary 1.
The time between the stop bit of one character and the start bit of the next character may be of
any duration. The data interchange circuit is in the marking condition between characters.
The default character structure consists of one start bit, eight data bits, no parity bit, and one
stop bit. Other character structures are supported, such as seven data bits and odd parity or seven
data bits and even parity.
The character bit sequencing, structure, and parity sense definitions conform to ANSI standards
X3.15-1976 and X3.16-1976.
Electrical Characteristics
The voltage and impedance levels for the generator and receiver circuits conform to the EIA-
232-D-1986 standard.
2–2 Clinitek Advantus and Clinitek 500 Interface Specification: Data Flow
04826807 Rev. A
Interface Connections
The Clinitek Advantus and Clinitek 500 support the connector requirements of ANSI standard
E1381-91.
Signal Levels
For the data interchange circuits, a marking condition corresponds to a voltage more negative
than minus three volts with respect to signal ground at the interface point. A spacing condition
corresponds to a voltage more positive than plus three volts with respect to signal ground at the
interface point.
Binary state ONE (1) corresponds to the marking condition; binary state ZERO (0) corresponds
to the spacing condition.
The signal levels conform to the EIA-232-D-1986 standard.
Speed
The default data transmission rate is 9600 baud. The data transmission rates supported are 2400,
4800, 9600, and 19200.
Data Link Layer
The data link layer contains the procedures for link connection and release, delimiting and
synchronism, sequential control, error detection, and error recovery.
The Clinitek Advantus and Clinitek 500 use a simple data link protocol. The data link protocol
is designed for sending character based message text. Restrictions are placed on which
characters may appear in the message text. The restrictions make it simpler for senders and
receivers to recognize replies and frame delimiters. Additional characters are restricted to avoid
interfering with software controls for devices such as multiplexers.
Data Characters
The control characters that the computer sends to the analyzer to manage the data flow are
shown in Table 2-1.
NOTE:Depending on the analyzer configuration, the computer uses either the <ENQ> or the
<BEL> character to initiate the request for identification.
Clinitek Advantus and Clinitek 500 Interface Specification: Data Flow 2–3
04826807 Rev. A
Table 2-1 Data Flow Control Characters
The characters that the analyzer and computer use to communicate data sets are shown in Table
2-2.
Table 2-2 Data Set Control Characters
Data Transfer Phases
The data link mode of operation is a one-way transfer of information with alternative
supervision. Information flows in one direction at a time. Replies occur after information is sent,
never at the same time. It is a simplex stop-and-wait protocol.
At times both systems are actively operating to transfer information - one side sending and the
other side receiving. The remainder of the time the data link is in a neutral state waiting for one
of the sides to request control.
There are three distinct phases in transferring information between the Clinitek analyzer and a
laboratory computer system:
•Establishment Phase (Link Connection)
•Data Transfer Phase
•Termination Phase (Link Release)
In each phase, one side directs the operation and is responsible for continuity of communication.
The three distinct phases assure the actions of sender and receive are coordinated. Control
Code Control Function
<ENQ> ASTM request for identification message
<BEL> single character request for identification message
<ACK> Receiving system, either computer or analyzer acknowledges the
receipt of the message.
<NAK> Computer did not receive the data correctly, analyzer not to
address the next data set.
Control Code Control Function
<STX> Start of text character
<CR> Carriage return character
<LF> Line feed character
<EOT> End of text character
04826807 Rev. A
Establishment Phase (Link Connection)
The establishment phase determines the direction of information flow and prepares the receiver
to accept information. The system with information available initiates the establishment phase.
After the sender determines the data link is in a neutral state, it transmits the <ENQ>
transmission control character to the intended receiver.
Upon receiving the <ENQ>, the receiver must respond to the sender before the sender can begin
sending information. If the receiver is able to receive information, it responds with an <ACK>
transmission control character signifying that it is ready. With this sequence of events, the
establishment phase ends and the transfer phase begins.
If the receiver cannot immediately receive information from the sender, the receiver replies with
a <NAK> transmission control character. Upon receiving <NAK>, the sender must wait at least
10 seconds before again attempting to establish a communication link by transmitting another
<ENQ>.
If both systems simultaneously attempt to start a communication session by transmitting an
<ENQ>, the data link is considered to be in contention. The Clinitek analyzer has priority to
transmit information when contention occurs. The contention to start a communication session
is resolved as follows:
Upon receiving a reply of <ENQ> to its transmitted <ENQ>, the computer system must stop
trying to transmit; it must prepare to receive. The computer sets a timer. If an <ENQ> is not
received from the Clinitek analyzer within 20 seconds, a time-out occurs. After a time-out, the
receiver regards the line to be in the neutral state and may again attempt to acquire the line by
sending an <ENQ> to the Clinitek analyzer. If, however, the computer receives an <ENQ> from
the Clinitek analyzer within the 20-second period, it must reply with an <ACK> or <NAK>
depending on its readiness to receive information.
Upon receiving a reply of <ENQ> to its transmitted <ENQ>, the Clinitek analyzer must wait at
least 1 second before sending another <ENQ>.
Transfer Phase
During the transfer phase, the sender transmits messages to the receiver. The transfer phase
continues until all the messages have been sent.
Frames
Each message is sent in a series of frames. A frame is a pre-defined subdivision of a message
used to provide for periodic communication housekeeping such as error checks and
acknowledgments. Each frame contains a maximum of 247 characters (including frame
overhead). Messages longer than 240 characters are divided between two or more frames. Both
the sender and receiver must be able to buffer one complete frame (247 characters).
04826807 Rev. A
Multiple messages are never combined in a single frame. Every message must begin in a new
frame. Records are never split across frames.
A frame is one of two types, an intermediate frame or an end frame. Intermediate frames
terminate with the characters <ETB>, checksum, <CR> and <LF>. End frames terminate with
the characters <ETX>, checksum, <CR> and <LF>. Messages less than 240 characters may be
sent in one end frame. Longer messages are sent in intermediate frames with the last part of the
message sent in an end frame.
The frame structure is as follows:
<STX> FN text <ETB> C1 C2 <CR> <LF> <-- intermediate frame
.
.
<STX> FN text <ETX> C1 C2 <CR> <LF> <-- end frame
where:
Frame Number
The frame number allows the receiver to distinguish between new and retransmitted frames. It is
a single digit sent immediately after the <STX> character.
The frame number is an ASCII digit ranging from 0 to 7. The frame number begins at 1 with the
first frame of the Transfer phase. The frame number is incremented by one for every new frame
transmitted. After 7, the frame number rolls over to 0, and continues in this fashion.
<STX> Start of Text transmission control character
FN single digit Frame Number 0 to 7
text Data Content of Message
<ETB> End of Transmission Block transmission control character
<ETX> End of Text transmission control character
C1 most significant character of checksum 0 to 9 and A to F
C2 least significant character of checksum 0 to 9 and A to F
<CR> Carriage Return ASCII character
<LF> Line Feed ASCII character
04826807 Rev. A
Checksum
The checksum permits the receiver to detect a defective frame. The checksum is encoded as two
characters which are sent after the <ETB> or <ETX> character. The checksum is computed by
adding the binary values of the characters, keeping the least significant eight bits of the sum.
The checksum is initialized to zero with the <STX> character. The first character used in
computing the checksum is the frame number. Each character in the message text is added to the
checksum (modulo 256). The computation for the checksum does not include <STX>, the
checksum characters, or the trailing <CR> and <LF>.
The checksum is an integer represented by eight bits, it can be considered as two groups of four
bits. The groups of four bits are converted to the ASCII characters of the hexadecimal
representation. The two ASCII characters are transmitted as the checksum, with the most
significant character first.
For example, a checksum of 122 can be represented as 01111010 in binary or 7A in
hexadecimal. The checksum is transmitted as the ASCII character 7 followed by the character
A.
Acknowledgments
The sender sends one frame at a time. After a frame is sent, the sender stops transmitting until a
reply is received. When the sender has transmitted the last character of a frame, it sets a timer.
The receiver must reply to each frame sent within 15 seconds. If the sender has not received an
<ACK>, a <NAK>, or an <EOT> in response to the frame sent within the 15-second time
period, the sender enters the termination phase of the communication session by sending an
<EOT>.
A reply of <ACK> from the receiver signifies the frame was received successfully and the
receiver is prepared to receive another frame. The sender then increments the frame number and
sends the next frame or terminates the communication session.
A reply of <NAK> from the receiver signifies the frame was not successfully received and the
receiver is prepared to receive the frame again. Upon receiving a <NAK> in response to a
frame, the sender increments a retransmit counter and retransmits the frame. If this counter
shows a single frame was sent and not accepted six times, the sender stops attempting to send
the frame and proceeds to the termination phase of the communication session by sending an
<EOT>.
A reply of <EOT> from the receiver tells the sender the frame was received successfully but
does not want to continue the communication session. It is a request to the sender to stop
transmitting. After receiving the receiver interrupt request, the sender sends the Message
Terminator record and ends the communication session.
04826807 Rev. A
During the transfer phase, if the receiver responds to a frame with an <EOT> in place of the
usual <ACK>, the sender interprets this reply as a receiver interrupt request. The <EOT> is a
positive acknowledgment of the end frame and also a request to the sender to stop transmitting.
The sender then enters the termination phase to return the data link to the neutral state. This
gives the receiver an opportunity to enter the establishment phase and become the sender. The
original sender must not enter the establishment phase for at least 15 seconds or until the
receiver has sent a message and returned the data link to the neutral state.
If the receiver requests the sender to stop transmitting results before all the result records have
been sent and acknowledged for a patient, ALL the results for that patient must be retransmitted
the next time results are sent. If the receiver requests the sender to stop transmitting results after
the last result is sent for a patient, the next result transmission begins with the next patient
record.
Termination Phase (Link Release)
The termination phase returns the data link to the clear or neutral state. The sender notifies the
receiver that all messages have been sent.
The sender transmits the <EOT> transmission control character and then regards the data link to
be in a neutral state. Upon receiving <EOT>, the receiver also regards the data link to be in the
neutral state.
Error Handling
A receiver checks every frame to guarantee it is valid. A reply of <NAK> is transmitted for
invalid frames. Upon receiving the <NAK>, the sender must retransmit the last frame with the
same frame number.
Any characters occurring before the <STX> or after the end of the block character (the <ETB>
or <ETX>) are ignored by the receiver when checking the frame.
The receiver should reject a frame when:
•A character error is detected (parity error, framing error, etc.)
•The frame checksum sent does not match the checksum computed on the received frame
•The frame number is not the same as the frame number for a previously rejected frame or the
frame number is not one higher than the last accepted frame (modulo 8).
Upon receiving a <NAK>, the sender increments a retransmit counter and retransmits the frame.
If the retransmit counter shows a single frame was sent and not accepted six times, the sender
must abort the message by proceeding to the termination phase.
04826807 Rev. A
Timeouts
Both sender and receiver use timers to detect loss of coordination between them. The timer
provides a method for recovery if the communication line or the other device fails to respond.
Establishment Phase Timeouts
During the establishment phase, the sender sets a timer when transmitting the <ENQ>. If a reply
of an<ACK>, <NAK>, or <ENQ> is not received within 15 seconds, a timeout occurs. After a
timeout, the sender enters the termination phase.
During the establishment phase, if the computer (as receiver) detects contention, it sets a timer.
If an <ENQ> is not received within 20 seconds, a timeout occurs. After a timeout, the receiver
regards the line to be in the neutral state.
Transfer Phase Timeouts
During the transfer phase, the sender sets a timer when transmitting the last character of a frame.
If a reply is not received within 15 seconds, a timeout occurs. After a timeout, the sender aborts
the message transfer by proceeding to the termination phase. As with excessive transmission of
defective frames, the message must be retained so that it can be completely retransmitted.
During the transfer phase, the receiver sets a timer when first entering the transfer phase or
when replying to a frame. If a frame or <EOT> is not received within 30 seconds, a timeout
occurs. After a timeout, the receiver discards the last incomplete message and regards the line to
be in the neutral state.
A receiver must reply to a frame within 15 seconds or the sender will abort the message and a
time out occurs.
Message Structure
This section describes the supported message types, the structure of those message types and
their supporting records. Each message consists of a hierarchy of records of various types.
The following rules apply when the analyzers are processing a message:
•The laboratory computer system may ignore any field it does not require.
•All fields in a record are always transferred.
•The fields are always transferred in the positional order specified
•All fields in records are variable length fields.
04826807 Rev. A
Supported Record Types
Both the Clinitek Advantus and Clinitek 500 analyzers support similar record types with the
Clinitek Advantus supporting one additional record type. Table 2-3 describes the supported
record types.
Table 2-3 Supported Record Types
Record Type Description
Message Header Record marks the beginning of a message
It is always the first record sent in a message.
Request for Identification Record initiated by the laboratory computer
Two different types of sessions are supported: a
standard ASTM messaging session and a simple,
single character message session.
Patient Record contains information about a sample that applies to
every Result record for that sample
Result Record contains the result of a single test determination.
Because Clinitek urine chemistry test strips contain
multiple chemistry tests, the analyzer reports one
result record for each result.
Message Terminator Record signals the end of the record
If transmission terminates prior to the Message
Terminator record being received and
acknowledged, the entire message must be
retransmitted in a new session. That is, the patient
records and all result records for that patient must
be retransmitted.
Order Record
(Only the Clinitek Advantus
analyzer supports this record.)
sent by the computer system to the analyzer
The order record provides the Clinitek Advantus
analyzer with a list of sample IDs for which tests to
perform.
The functionality of the record only allows the
remote computer to send a list of Sample IDs. It
cannot send any additional information.
04826807 Rev. A
Communication Sessions
The Clinitek Advantus and Clinitek 500 analyzers support the following types of
communication sessions:
•Request for Identification session
•Order Communication Session (Clinitek Advantus analyzer only)
•Results Reporting session
Request for Identification Communication Session
The computer or LIS initiates the Request for Identification communication session. Two
different types of sessions are supported:
•standard ASTM messaging session
•single character message session
Standard ASTM Identification Request Session
The standard ASTM identification request session uses two types of messages:
•request information message sent by the computer or LIS
•identification message response sent by the analyzer
ASTM Request Information Message
The computer or LIS sends the request information message using the following logical
structure:
•message header record
•request information record
The computer or LIS must send the request information record to the analyzer in a separate field
from the message header record.
NOTE:The computer or LIS does not send a message terminator record after the request
information record. The analyzer sends the message terminator after replying to the request
information query.
ASTM Identification Message Response
The analyzer sends the identification message response using the following logical structure:
•message terminator record
If transmission is terminated before the computer receives and acknowledges the message
terminator record, you must resend the entire message in a new session.
04826807 Rev. A
ASTM Communication Session
The ASTM communication session follows the pattern displayed in this table:
Table 2-4 Clinitek Advantus and Clinitek 500 ASTM Communication
Analyzer Dir. Computer or LIS
Send <ENQ> to acquire the line
<ACK>
Send Header field
<ACK>
Send Request for Identification
<ACK>
Send Identification (Header)
<ACK>
Send Message termination
<ACK>
Send <EOT> to release the line
04826807 Rev. A
ASTM Data Exchange
An example of actual data exchanged for the standard ASTM identification request session
appears as shown in the following table:
Table 2-5 ASTM Data Exchange
NOTE:On the Clinitek Advantus, the manufacturer is Siemens Medical Solutions Diagnostics,
the product ID is 1420, and the analyzer serial number is after the product ID in the analyzer
transmission.
Single Character Identification Request Session
The single character identification request session uses two types of messages:
•<BEL> character request message sent by the computer or LIS
•identification message response sent by the analyzer.
Single Character Request Message
The computer or LIS sends the request information message using the <BEL> character.
NOTE:The computer or LIS does not send a message terminator record after the request
information record. The analyzer sends the message terminator after replying to the request
information query.
Row Analyzer Computer or LIS
1.
2. <ENQ>
3. <ACK>
4. <STX>1 H|\^&|||Laboratory
Computer System Name||||||
|P|1|19970526101230<CR>
<ETX>C1 C2<CR><LF>
5. <ACK>
6. <STX>2 Q|1<CR> <ETX>C1
C2<CR><LF>
7. <ACK>
8. <STX>1
H|\^&|||BAYER^6740^^01.00/
01.00||||||010|P|1|1997052610130
0<ETX>C1 C2<CR><LF>
9. <ACK>
10. <STX>2 L|1|N<CR> <ETX>C1
C2<CR><LF>
11. <ACK>
12. <EOT>
04826807 Rev. A
Single Character Identification Message Response
The analyzer sends the identification message response using the following logical structure:
•message terminator record
Single Character Communication Session
The single character communication session follows the pattern displayed in this table:
Table 2-6 Single Character Communication Session
Single Character Data Exchange
An example of actual data exchanged for the single character identification request session
appears as shown in the following table:
Table 2-7 Single Character Data Exchange
NOTE:On the Clinitek Advantus, the manufacturer is Siemens Medical Solutions Diagnostics,
the product ID is 1420, and the analyzer serial number is after the product ID in the analyzer
transmission.
Analyzer Dir. Computer or LIS
Send <BEL> character
Send identification (Header)
<ACK>
Send message termination
<ACK>
Send EOT to release the line
1.
2. <BEL>
3. <ACK>
4. <STX>1
H|\^&|||BAYER^6740^^01.00/
01.00||||||010|P|1|1997052610130
0<ETB>C1 C2<CR><LF>
5. <ACK>
6. <STX>2 L|1|N<CR> <ETX>C1
C2<CR><LF>
7. <ACK>
8. <EOT>
04826807 Rev. A
Order Communication Session
NOTE:Only the Clinitek Advantus analyzer supports the Test Order record.
The Order communication session is initiated by the computer or LIS. The Order
Communication session sends worklist information to the analyzer.
The computer or LIS sends the order information message using the following logical structure:
•Message Header
• Order Record 1
• Order Record 2
• Order Record n
•Message Terminator
Order Communication Session
The order communication session follows the pattern displayed in this table:
Table 2-8 Order Communication Session
Clinitek Advantus Analyzer Flow Computer or LIS
<ACK>
Send Header record
<ACK>
Send first Order record
<ACK>
Send second Order record
<ACK>
Send nth Order record
<ACK>
Send Message Termination record
<ACK>
04826807 Rev. A
Order Data Exchange
An example of actual data exchanged for the order session appears as shown in the following
table:
Table 2-9 Order Data Exchange
1. <ENQ>
2. <ACK>
3. <STX>1 H|\^&|||Laboratory Computer System Name||||||
|P|1|20051007132700<CR> <ETX>C1 C2<CR><LF>
4. <ACK>
5. <STX>2 O|1|1234567890123<CR>
O|2|1234567890123<CR>
O|3|1234567890124<CR>
O|4|1234567890125<CR>
O|5|1234567890126<CR>
O|6|1234567890127<CR>
O|7|1234567890128<CR>
O|8|1234567890129<CR>
O|9|1234567890130<CR>
O|10|1234567890131<CR>
O|11|1234567890132<CR>
O|12|1234567890133<CR>
O|13|1234567890134<CR>
<ETB>C1 C2<CR><LF>
6. <ACK>
7. <STX>3 O|14|1234567890135<CR>
O|15|1234567890136<CR>
O|16|1234567890137<CR>
O|17|1234567890138<CR>
O|18|1234567890139<CR>
O|19|1234567890140<CR>
O|20|1234567890141<CR>
O|21|1234567890142<CR>
O|22|1234567890143<CR>
O|23|1234567890144<CR>
O|24|1234567890145<CR>
O|25|1234567890146<CR>
<ETB>C1 C2<CR><LF>
8. <ACK>
Table continues on the next page.
04826807 Rev. A
9. <STX>4 O|26|1234567890147<CR>
O|27|1234567890148<CR>
O|28|1234567890149<CR>
O|29|1234567890150<CR>
O|30|1234567890151<CR>
O|31|1234567890152<CR>
O|32|1234567890153<CR>
O|33|1234567890154<CR>
O|34|1234567890155<CR>
O|35|1234567890156<CR>
O|36|1234567890157<CR>
O|37|1234567890158<CR>
<ETB>C1 C2<CR><LF>
10. <ACK>
11. <STX>5 O|38|1234567890159<CR>
O|39|1234567890160<CR>
O|40|1234567890161<CR>
O|41|1234567890162<CR>
O|42|1234567890163<CR>
O|43|1234567890164<CR>
O|44|1234567890165<CR>
O|45|1234567890166<CR>
O|46|1234567890167<CR>
O|47|1234567890168<CR>
O|48|1234567890169<CR>
O|49|1234567890170<CR>
<ETB>C1 C2<CR><LF>
12. <ACK>
13. <STX>6 O|50|1234567890171<CR>
<ETX>C1 C2<CR><LF>
14. <ACK>
15. <EOT>
04826807 Rev. A
Results Reporting Communication Session
The Results Reporting communication session is initiated by the analyzer. When the analyzer
has a test result to transmit, it notifies the computer or LIS. When the computer or LIS
acknowledges the analyzer, the analyzer transmits the test results.
The analyzer transmits the results message using the following logical structure:
•Header
• Patient 1
Result 1
Result 2
...
Result n
•Header
• Patient 2
Result 1
Result 2
...
Result n
terminator record, you must resend the patient records and all result records for that patient.
Results Communication Session
The results communication session follows the pattern displayed in this table:
Table 2-10 Order Communication Session
Analyzer Flow Computer or LIS
<ACK>
Send Header frame
<ACK>
Send first Patient frame
<ACK>
Send first Result frame
<ACK>
Send any additional Result frames
<ACK>
04826807 Rev. A
The Order Communication session treats each patient record as an independent communication
session. The analyzer transmits an <ENQ> to acquire the line to transmit the next patient record
for each patient record that is available for transmission.
Results Data
To illustrate the transfer of data from the Clinitek Advantus and Clinitek 500 analyzers to a
computer or LIS, the following illustration displays actual results data assuming these
parameters:
•urine chemistry test type is MULTISTIX 10 SG
•color is reported
•clarity is not reported
•all chemistry tests on the strip are reported.
•three tests are run
Send Message Termination record
<ACK>
Send next <ENQ> to initiate next
patient
or
Analyzer Flow Computer or LIS

04826807 Rev. A
00001 05-26-07 10:25 AM
Tech ID: 323
ID: 312445446
COL YELLOW
* GLU 250 mg/dL
BIL NEGATIVE
! KET NEGATIVE
SG <=1.005
* BLO SMALL
pH 6.0
PRO NEGATIVE
URO 1.0 E.U./dL
NIT NEGATIVE
* LEU TRACE
00002 05-26-07 10:25 AM
Tech ID: 323
ID: 213543331
COL YELLOW
GLU NEGATIVE
BIL NEGATIVE
KET NEGATIVE
SG <=1.005
BLO NEGATIVE
pH 5.5
PRO NEGATIVE
URO 0.2 E.U./dL
NIT NEGATIVE
LEU NEGATIVE
00003 05-26-97 10:25 AM
Tech ID: 323
ID: 398576435
* COL RED
GLU NEGATIVE
BIL NEGATIVE
KET NEGATIVE
SG <=1.005
* BLO MODERATE
pH 6.0
PRO NEGATIVE
URO 1.0 E.U./dL
NIT NEGATIVE
* LEU LARGE
04826807 Rev. A
Results Data Exchange
An example of actual data exchanged for the order session appears as shown in the following
table:
Table 2-11 Results Data Exchange
Row Analyzer
Computer or
LIS
1.
2. <ENQ>
3. <ACK>
4. <STX>1 H|\^&|||BAYER^6740^^01.00/
01.00||||||010|P|1|19970526102500<CR> <ETX>C1
C2<CR><LF>
5. <ACK>
6. <STX>2 P|1|00001|19970526102500|312445446|323<CR>
P|2|C|P|MULTISTIX 10 SG|F|0000<CR>
<ETX>C1 C2<CR><LF>
7. <ACK>
8. <STX>3 R|1|N|COL|12|YELLOW|1|0|A<CR>
R|2|A|GLU|1|250^mg/dL|3|0|A<CR>
R|3|N|BIL|2|NEGATIVE|1|0|A<CR>
R|4|N|KET|3|NEGATIVE|1|0|E<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
R|6|A|BLO|9|SMALL|4|0|A<CR>
<ETB>C1 C2<CR><LF>
9. <ACK>
10. <STX>4 R|7|N|pH|5|6.0|3|0|A<CR>
R|8|N|PRO|6|NEGATIVE|1|0|A<CR>
R|9|N|URO|7|1.0Ê.U./dL|2|0|A<CR>
R|10|N|NIT|8|NEGATIVE|1|0|A<CR>
R|11|A|LEU|10|TRACE|2|1|0<CR>
<ETB>C1 C2<CR><LF>
11. <ACK>
12. <STX>5 L|1<CR> <ETX>C1 C2<CR><LF>
13. <ACK>
14. <EOT> <ENQ>
15. <ACK>
16. <STX>1 H|\^&|||BAYER^6740^^01.00/
01.00||||||010|P|1|19970526102600<CR> <ETX>C1
C2<CR><LF>
04826807 Rev. A
17. <ACK>
18. <STX>2 P|1|00002|19970526102500|213543331|323<CR>
<ETX>C1 C2<CR><LF>
19. <ACK>
R|2|N|GLU|1|NEGATIVE|1|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
R|6|N|BLO|9|NEGATIVE|1|0|A<CR>
<ETB> C1 C2<CR><LF>
21. <ACK>
22. <STX>4 R|7|N|pH|5|5.5|2|0|A<CR>
R|9|N|URO|7|0.2Ê.U./dL|1|0|A<CR>
R|11|N|LEU|10|NEGATIVE|1|0|A<CR>
<ETB>C1 C2<CR><LF>
23. <ACK>
24. <STX>5 L|1<CR> <ETX>C1 C2<CR><LF>
25. <EOT> <ENQ>
26. <ACK>
27. <STX>1 H|\^&|||BAYER^6740^^1.00/
01.00||||||010|P|1|19970526102500<CR> <ETX>C1
C2<CR><LF>
28. <ACK>
29. <STX>2 P|1|00003|19970526102500|398576435|323<CR>
<ETX>C1 C2<CR><LF>
30. <ACK>
31. <STX>3 R|1|A|COL|12|RED|3|1|A<CR>
R|4|N|KET|3|NEGATIVE|1|1|A<CR>
R|5|N|SG|4|<=1.005|1|1|A<CR>
R|6|A|BLO|9|MODERATE|4|1|A<CR>
<ETB> C1 C2<CR><LF>
32. <ACK>
Row Analyzer
Computer or
LIS

04826807 Rev. A
NOTE:On the Clinitek Advantus, the manufacturer is SIEMENS, the product ID is 1420, and
the analyzer serial number is included after the product ID in the analyzer transmission.
Resending the Results Frame
If the laboratory computer calculates a different checksum value for a frame, the computer must
refuse to accept that frame and the analyzer must resend the frame. The analyzer may send the
frame a maximum of six times. If the frame is not accepted after the sixth transfer of the frame,
the analyzer must terminate the communication session. The analyzer may then initiate a new
session.
Table 2-12 displays a retransmission of the third results frame from the previous example. In
this instance, the laboratory computer does not calculate the same checksum value as that sent
by the analyzer for the third frame (line 7). The laboratory computer refuses to accept the frame
(<NAK>), and the Analyzer resends that frame.
33. <STX>4 R|7|N|pH|5|6.0|3|1|A<CR>
R|9|N|URO|7|1.0Ê.U./dL|2|1|A<CR>
R|11|A|LEU|10|LARGE|5|1|A<CR>
<ETB>C1 C2<CR><LF>
34. <ACK>
35. <STX>5 L|1|N<CR> <ETX>C1 C2<CR><LF>
36. <ACK>
37. <EOT>
Row Analyzer
Computer or
LIS
04826807 Rev. A
Table 2-12 Resending Results Data Exchange
Row Analyzer
Computer or
LIS
1. <ENQ>
2. <ACK>
3. <STX>1 H|\^&|||BAYER^6740^^1.00/
01.00||||||010|P|1|19970526102500<CR> <ETX>C1
C2<CR><LF>
4. <ACK>
5. <STX>2 P|1|00003|19970526102500|398576435|323<CR>
P|2|C|P|MULTISTIX 10 SG|F|0000<CR> <ETX>C1
C2<CR><LF>
6. <ACK>
7. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
8. <NAK>
9. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
10. <ACK>
11. <STX>4 R|7|N|pH|5|6.0|3|0|A<CR>
R|9|N|URO|7|1.0Ê.U./dL|2|0|A<CR>
R|11|A|LEU|10|LARGE|5|0|A<CR>
<ETB>C1 C2<CR><LF>
12. <ACK>
13. <STX>5 L|1|N<CR> <ETX>C1 C2<CR><LF>
14. <ACK>
15. <EOT>
04826807 Rev. A
After six attempts, if the third frame is not successfully retransmitted, the data exchange ends as
in Table 2-13. In Table 2-13, when the analyzer initiates a new session to send results, the
patient records and all the result records for the third patient must be sent again.
Table 2-13 Unsuccessful Resend Data Exchange
Row Analyzer
Computer or
LIS
1. <ENQ>
2. <ACK>
3. <STX>1 H|\^&|||BAYER^6740^^1.00/
01.00||||||010|P|1|19970526102500<CR> <ETX>C1
C2<CR><LF>
4. <ACK>
5. <STX>2 P|1|00003|19970526102500|398576435|323<CR>
P|2|C|P|MULTISTIX 10 SG|F<CR> <ETX>C1
C2<CR><LF>
6. <ACK>
7. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
8. <NAK>
9. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
10. <NAK>
11. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
12. <NAK>
04826807 Rev. A
Communication when the Computer Refuses Transmission
A problem can also occur on the laboratory computer side of the communication session
making it impossible for the computer to continue to receive the test results from the Analyzer.
The laboratory computer transmits an <EOT> instead of an <ACK> to notify the analyzer that it
cannot continue to receive results.
If the laboratory computer asks to terminate the communication session before the analyzer
transmits all the result records for a patient, the analyzer must resend all the information for that
patient the next time it reports results.
If the laboratory computer asks to end a results reporting session after receiving the termination
for a particular message, the next time the computer report results, the analyzer does not have to
resend that message and may begin with the next set of results.
13. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
14. <NAK>
15. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
16. <NAK>
17. <STX>3 R|1|A|COL|12|RED|3|0|A<CR>
R|5|N|SG|4|<=1.005|1|0|A<CR>
<ETB> C1 C2<CR><LF>
18. <NAK>
19. <EOT>
Row Analyzer
Computer or
LIS
04826807 Rev. A
The analyzer must wait at least 15 seconds before attempting to take control of the line again
and send additional results. When the analyzer does send an <ENQ> and receives a reply of
<ACK> from the laboratory computer, the analyzer transmits the next set of results.
Using the previously illustrated communication session, the information in
Table 2-14 assumes that after the transmission of the first result, the laboratory computer is
unable to continue to receive results.
Table 2-14 Communication when the LIS NAKS
Row
Analyzer
Computer or
LIS
1.
2. <ENQ>
3. <ACK>
4. <STX>1 H|\^&|||BAYER^6740^^1.00/
01.00||||||010|P|1|19970526102500<CR> <ETX>C1
C2<CR><LF>
5. <ACK>
6. <STX>2 P|1|00001|19970526102502|312445446|323<CR>
P|2|C|P|MULTISTIX 8|F|0000<CR> <ETX>C1
C2<CR><LF>
7. <ACK>
R|2|A|GLU|1|250^mg/dL|3|1|A<CR>
R|5|N|SG|4|<=1.005|1|1|A<CR>
R|6|A|BLO|9|SMALL|4|1|A<CR>
<ETB>C1 C2<CR><LF>
9. <ACK>
10. <STX>4 R|7|N|pH|5|6.0|3|1|A<CR>
R|9|N|URO|7|1.0Ê.U./dL|2|1|A<CR>
R|11|A|LEU|10|TRACE|2|1|A<CR> <ETB>C1
C2<CR><LF>
11. <ACK>
12. <EOT>
04826807 Rev. A
3 Formatting Test Records

This section of the Clinitek Advantus and Clinitek 500 Interface Specification provides the
information used to format the records that the analyzers support.
NOTE:Some analyzer versions show Bayer in the record content. This a vestige of programming
and does not imply any connection or relationship between Bayer and Siemens.
Record Structure and Content
This part of the specification defines the conventions for structuring the content of the records
and for representing the data elements contained within those structures.
The Clinitek Advantus and Clinitek 500 support the following types of records:
•Message Header Record
•Message Terminator Record
•Request Information Record
•Order Record (Clinitek Advantus only)
•Patient Record
•Result Record
All message data is represented as eight bit values within the range (0-126) as defined by the
ASCII standard (ANSI X3.4-1986).
Restricted Characters
Table 3-1 identifies the characters that may not appear in message text.
3–2 Clinitek Advantus and Clinitek 500 Interface Specification: Formatting Test Records
04826807 Rev. A
Table 3-1 Restricted Characters
Within text data fields, only ASCII characters 32-126 are permitted as usable characters with
the exception of those characters used as delimiter characters. The sender is responsible for
screening all text data fields to ensure that the text does not contain delimiter characters. The
contents of the data fields is case sensitive.
Fields are identified by their position within a record. The position is obtained by counting field
delimiters from the front of the record. This position-sensitive identification process requires
that when the contents of the field are null, its corresponding field delimiter must be included in
the record to ensure that the ith field can be found by counting (i-1) delimiters. Delimiters are
not included for trailing null fields; that is, if the tenth field was the last field containing data,
the record could terminate after the tenth field, and therefore would contain only nine delimiters.
Table 3-2 describes the delimiter characters.
Character ASCII Value HEX Value
<SOH> 001 01
<STX> 002 02
<ETX> 003 03
<EOT> 004 04
<ENQ> 005 05
<ACK> 006 06
<BEL> 007 07
<LF> 010 0A
<CR> 013 0D
<DLE> 016 10
<DC1> 017 11
<DC2> 018 12
<DC3> 019 13
<DC4> 020 14
<NAK> 021 15
<SYN> 022 16
<ETB> 023 17
Clinitek Advantus and Clinitek 500 Interface Specification: Formatting Test Records 3–3
04826807 Rev. A
Table 3-2 Message Delimiter Characters
Transmitted records may include more fields than are required by the receiving system. When
processing a record, the receiving system may ignore any field it does not require. All fields in a
record are always transferred, and the fields are always transferred in the positional order
specified to facilitate accurate identification by the computer system.
All fields in records are variable length fields.
For all record types, dates are recorded in YYYYMMDD format and times are represented as
HHMMSS.
Date and time together are specified as a fourteen-character string: YYYYMMDDHHMMSS.
Delimiter
Character
Representation Definition
Record Delimiter Carriage Return <CR>
(ASCII 13)
The record delimiter marks the end of
each record.
Field Delimiter Vertical Bar (|)
(ASCII 124)
The field delimiter is used to separate
adjacent fields.
Repeat Delimiter Backslash (\)
(ASCII 92)
The repeat delimiter is used to separate
variable numbers of descriptors for fields
containing parts of equal members of the
same set.
Component
Delimiter
Caret (^)
(ASCII 94)
The component delimiter is used to
separate data elements within a field.
Escape Delimiter Ampersand (&)
(ASCII 38)
The escape delimiter is used within text
fields to signify special case operations.
Applications of the escape delimiter are
optional and may be used or ignored at
the discretion of either the transmitter or
the receiver. All applications must accept
the escape delimiter and use it to
correctly parse fields within the record.
04826807 Rev. A
Message Header Record Format
The Message Header record consists of 15 fields of information with each field in a predefined
position as described in Table 3-3.
Table 3-3 Message Header Record
Field Record Description
1. Record type H indicates a Message Header record type.
2. Delimiter
definition
5 ASCII characters that define the delimiters used for all
record types.
• field delimiter (|)
• repeat delimiter (\)
• component delimiter (^)
• escape delimiter (&)
• carriage return to start a new line
3. Message control
ID
The Clinitek Communication Standard does not use this
field and its position is represented by the field delimiter.
When used, this field contains unique characters
identifying the transmission for use in network systems
having defined acknowledgement protocols outside the
scope of ASTM Specification E1394.
4. Access password The Clinitek Communication Standard does not use this
When used, this field is a password as mutually agreed
upon by the sender and receiver.
5. Sender name A component field containing the following elements:
• manufacturer (required field)
• analyzer product code (required field)
For Clinitek Advantus, the code is 1420.
For Clinitek 500, the code is 6470.
• serial number
The serial number is a maximum of 7 digits. When
not used, the field displays component delimiters.
For Clinitek Advantus, this is a required field.
• software version
The software version is a required component.
6. Sender street
address
When used, this field contains the sender's street address.
7. Reserved field
8. Sender telephone
number
When used, this field contains the sender's telephone
number.
04826807 Rev. A
9. Characteristics of
the server
This field contains characteristics of the sender such as
parity, checksums, and optional protocols.
Because you provide this information in the instrument's
setup routine, this field does not always contain
information and may be represented by the field
delimiter.
10. Receiver ID The Clinitek Communication Standard does not use this
When used, this field contains the name or other ID of
the receiver and is used to verify that the transmission is
being received.
11. Comments This is a component field containing the language/result
unit code
Refer to Language/Result Unit Codes‚ page 3-6.
12. Processing ID This field indicates how to process the message:
• P for Production:
You may use the test results for patient tests.
In normal clinical use, this is the only processing ID
used.
• T for Training:
Test results obtained from this software are not for
clinical use.
• D for Debugging:
Test results obtained from this software are not for
clinical use.
• Q for Quality Control:
Used for obtaining quality assurance or regulatory
data.
Although the portions of the software that collect
and process the data are validated, the test results
obtained from this software are not for clinical use.
13. Version number This field is the version level of the Clinitek
Communication Standard Specification
This value is currently 1.
14. Date & Time of
message
This field contains the date and time this header record is
sent.
The format for this field is YYYYMMDDHHMMSS.
NOTE: For Clinitek Advantus, the seconds field is
always 00. For Clinitek 500, the seconds field records the
seconds.
15. <CR> Carriage return
04826807 Rev. A
Example of a Message Header Record
Clinitek Advantus software version V1.20/V1.00 and later:
H | \^& | | | SIEMENS^1420 ^100123 ^01.20:001/V1.00 | | | | | | 010 | P | 1|
20070306102000 <CR>
Clinitek Advantus software version V1.00:001/V1.00:
H | \^& | | | BAYER^1420 ^100123 ^01.20:001/V1.00 | | | | | | 010 | P | 1|
20070306102000 <CR>
Clinitek 500 software:
H | \^& | | | BAYER^6470 ^^00.20/XP.11 | | | | | | 010 | P | 1| 19970526102000
<CR>
Language/Result Unit Codes
Field 11 of the Message Header record contains a code that indicates the language and the units
of measurements used for the record.
NOTE:To maintain compatibility with legacy instruments, the codes do not follow a logical
order.
Table 3-4 Language Unit Codes
Language Result Units Code
English Conventional - Normal 010
English Conventional - PLUS System 011
English S.I. - Normal 020
English S.I. - PLUS System 021
English Nordic - Normal 030
English Nordic - PLUS System 031
French Conventional - Normal 040
French Conventional - PLUS System 041
French S.I. - Normal 050
French S.I. - PLUS System 051
German Conventional - Normal 060
German Conventional - PLUS System 061
German S.I. - Normal 070
German S.I. - PLUS System 071
Italian Conventional - Normal 080
Italian Conventional - PLUS System 081
Japanese Conventional - Normal 090
Japanese Conventional - PLUS System 091
04826807 Rev. A
* Only available on the Clinitek Advantus
Message Terminator Record Format
The Message Terminator record consists of 4 fields of information with each field in a
predefined position as described in Table 3-5.
Spanish Conventional - Normal 100
Spanish Conventional - PLUS System 101
Chinese Conventional - Normal 110
Chinese Conventional - PLUS System 111
Chinese S.I. - Normal 120
Chinese S.I. - PLUS System 121
Portuguese Conventional - Normal 130
Portuguese Conventional - PLUS System 131
Japanese JCCLS - Normal 140
Japanese JCCLS - PLUS System 141
Italian* S.I. - Normal 150
Italian* S.I. - PLUS System 151
Spanish* S.I. – Normal 160
Spanish* S.I. - PLUS System 161
Portuguese* S.I. - Normal 170
Portuguese* S.I. - PLUS System 171
Swedish* Conventional - Normal 180
Swedish* Conventional - PLUS System 181
Swedish* S.I. - Normal 190
Swedish* S.I. - PLUS System 191
Swedish* Nordic - Normal 200
Swedish* Nordic - PLUS System 201
Language Result Units Code
04826807 Rev. A
Table 3-5 Message Terminator Record Table
Examples of a Message Terminator Record
The following line of text is an example of a Message Terminator record:
L | 1 | N <CR> or L | 1 <CR>
Request Information Record Format
The computer or LIS sends the request information record to request that the analyzer send a
Message Header record.
The request information record consists of 3 fields of information with each field in a
predefined position as described in Table 3-6.
Table 3-6 Request Information Record Table
Example of a Request Information Record
The following line of text is an example of a request information record:
Q | 1 <CR>
Pos Record Description
1. Record type L indicates a Message Terminator record type.
2. Record Sequence
Number
This is the nth occurrence of this record type within the
message.
Because this record uses only one Message Terminator
record per message, this field always has a value of 1.
3. Message Control ID This field contains a code indicating the reason the
message ended.
The valid termination codes are as follows:
• N or null field – normal termination
• T – sender aborted
• R – receiver requested abort
• E – unknown system error
• Q – error in last request for information
• I – no information available from last query
• F – last request for information processed
1. Record type Q indicates a request information record.
2. Record Sequence
Number
This field records the nth occurrence of this record type
within the message.
04826807 Rev. A
Order Record Format
NOTE:Only the Clinitek Advantus uses the Order Record.
The computer or LIS sends the order record to provide the analyzer with a worklist of Sample
IDs, listing the tests to be performed.
The order record consists of 4 fields of information with each field in a predefined position as
described in Table 3-7.
Table 3-7 Order Record Table
Examples of Order Record
The following lines of text are examples of an order record in Clinitek Advantus:
Analyzer Accepting only ID Information
O | 1 | 078302465 <CR>
Analyzer Accepting ID, Color, and Clarity
O | 1 | 078302465^YELLOW^CLEAR <CR>
1. Record type O indicates an order record.
2. Record Sequence
Number
message.
3. Patient Identification This is a component field.
NOTE: The Clinitek Advantus analyzer only accepts
Sample ID information and rejects any further
components.
The sample ID must be the first component in the
Patient Identification field.
The Sample ID field has no restriction on the number
of characters, however, the Clinitek Advantus only
accepts the first 13 values received. Any further
characters are truncated from the Sample ID.
04826807 Rev. A
Patient Record Format
The patient record contains information about a sample that applies to every result record for
that sample. The two formats that apply to patients are as follows:
•Test Sequence Format
•Results Format
Patient Record – Test Sequence Format
The test sequence format consists of the fields described in Table 3-8.
Table 3-8 Patient Record – Test Sequence
Example of the Patient Record – Test Sequence
The following line of text is an example of the patient record test sequence format:
P | 1 | 00001 | 19970526102000 | 312432216 | 34010 <CR>
1. Record type P indicates a patient record.
2. Record Sequence
Number
message.
3. Test Sequence
Number
This field contains the sequence number assigned to
this test strip by the analyzer.
• For patient results, the sequence number is 5
numeric characters.
• For control results, the sequence number is 4
numeric characters with a leading C.
4. Date and Time The date and time the test strip is read at the first
readhead.
The format is YYYYMMDDHHMMSS. The seconds
field is always 00.
5. Sample ID This field is optional.
If the Sample ID option is set to Off or if no Sample ID
is entered for this test, this field is empty.
If the Tech ID option is set to On, the field contains a
field delimiter.
6. Tech ID This field is optional.
If the Sample ID option is set to Off or if no Sample ID
is entered for this test, this field is empty.
If the Tech ID option is set to On, the field contains a
field delimiter.
7. Sample Location Not used.
04826807 Rev. A
Patient Record – Results Format
The results format consists of the fields described in Table 3-9.
Table 3-9 Patient Record – Results
Example of the Patient Record – Results Record
The following line of text is an example of the results record:
P | 2 | C | P | MULTISTIX 10 SG | F | 0000 <CR>
1. Record type P indicates a patient record.
2. Record Sequence
Number
message.
3. Results Format This field holds the code for the output format of the
results.
The results format is C for Clinical results.
4. Test Mode The Test Mode field defines the type of test being run.
For the Clinitek Advantus and Clinitek 500 analyzers,
the test mode can be P for Patient or C for Control.
5. Test Strip ID The Test Strip ID field defines the type of reagent test
strip used for the test.
Refer to Test Strip ID‚ page 3-12.
6. Transfer Status The Transfer Status field has two options:
• F for First Time Transfer
• R for User Requested Resend.
7. Error Code This field indicates the error condition of the record
and always contains a value.
• If valid results are calculated for the test strip, the
field contains 0000.
• If a problem is detected that prevents clinical
result values being reported, the field contains a
code identifying the source of the problem.
Refer to Error Codes‚ page 3-13.
8. Auxiliary
Information
Not transmitted in clinical mode.
04826807 Rev. A
Test Strip ID
The following table displays the supported test strips by analyzer.
Table 3-10 Test Strip IDs
Clinitek Advantus Clinitek 500
Multistix 10 SG (N Multistix SG-L) Multistix 10 SG
Multistix 9 Multistix 9
Multistix 9 SG Multistix 9 SG
Multistix 8 SG Multistix 8 SG
Multistix SG Multistix SG
Multistix SG L Multistix SG L
Multistix Multistix
N-Multistix SG N-Multistix SG
Nephrostix L Nephrostix L
Uro-Hemacombistix Uro-Hemacombistix
Uro-Hemacombistix SG L Uro-Hemacombistix SG L
Uro-Labstix Uro-Labstix
Uro-Labstix SG L Uro-Labstix SG
Hemacombistix – Long Uro-Labstix SG L
Lifestix Combistix SG – Long
Multistix PRO® 7G Hemacombistix – Long
Multistix PRO 10LB Uristix – Long
Multistix PRO 10LS Lifestix
Multistix PRO 11 Multistix PRO 6B
Clinitek Microalbumin 9 Multistix PRO 6K
Multistix PRO 7G
Multistix PRO 7pH
Multistix PRO 10
Multistix PRO 10LB
Multistix PRO 10LS
Multistix PRO 10SB
Multistix PRO 11
04826807 Rev. A
Error Codes
The error code field may contain a value that represents multiple errors. For example, if a low
dark value is detected under readhead 1 and a skewed strip is detected at readhead 2, the error
code is 0109.
Clinitek Advantus Error Codes
The following table displays the error codes used by the Clinitek Advantus analyzer:
Table 3-11 Clinitek Advantus Error Codes
Clinitek 500 Error Codes
The following table displays the error codes used by the Clinitek 500 analyzer:
Table 3-12 Clinitek 500 Error Codes
Error Codes
Error Readhead 1 Readhead 2
Low dark value 0100 0001
High dark value 0200 0002
A-D converter over-range 0300 0003
Low lamp(s) level 0400 0004
Low channel output 0500 0005
Missing strip N/A 0006
Upside down or dry strip 0700 N/A
Misaligned strip 0800 0008
Skewed strip 0900 0009
Reflectance > 100% 1000 0010
Auto strip type error 2000 N/A
Detected strip does not match expected value N/A 0020
Divide by zero error 3000 0030
Error Codes
Low dark value 0100 0001
High dark value 0200 0002
A-D converter over-range 0300 0003
Low lamp(s) level 0400 0004
Low channel output 0500 0005
Missing strip N/A 0006
Upside down or dry strip 0700 N/A
04826807 Rev. A
Result Record for Clinical Results Format
The result record contains the result of a single test determination. Because Clinitek urine
chemistry test strips contain multiple chemistry tests, there is one result record for each result
reported.
•If you are reporting color or clarity, these physical results are contained in a separate record.
•A result record may never appear without a preceding patient record.
•On the Clinitek Advantus, microscopic data entered by the user is also reported using the
results record.
This data field follows the fields reporting clinical, color, and clarity records.
•A maximum of six additional results are produced dependent upon the instrument
configuration.
The results format consists of the fields described in Table 3-13.
Table 3-13 Result Records
Misaligned strip 0800 0008
Skewed strip 0900 0009
Reflectance > 100% 1000 0010
Auto strip type error 2000 N/A
1. Record type P
2. Record sequence
number
The nth occurrence of this record type within the message
3. Test result status Indicates whether the result is normal or abnormal.
• If the result is within the normal range for the test, this
field contains an N.
• If the test result is outside the normal range for the
test, this field contains an A.
• For microscopic data results on the Clinitek Advantus
analyzer, this field reports N.
4. Test name
abbreviation
The abbreviation for the test or physical value.
Abbreviations are language dependent.
For microscopic data results on the Clinitek Advantus
analyzer, this field contains the header name as configured
by the user for the relevant microscopic data result.
Refer to Test Strip Assays and Abbreviations‚ page 3-16.
5. Test number ID A numeric value for the test.
Refer to Test Strip Assays and Abbreviations‚ page 3-16.
Error Codes
04826807 Rev. A
6. Test result value
and result unit of
measure
The clinical test result divided into a numerical component
and a result unit of measure component.
• For qualitative results such as positive, negative,
normal, normal dilute, clear, or yellow, the record
positions the result in the Test Result Value
component of the field.
The record does not use a component delimiter
because the Result Unit of Measure portion of the
field is empty.
• For color and clarity results, the record does not use a
component delimiter.
• For ratio results that contain a quantitative value and a
qualitative value (for example, P:C > 500 mg/g
abnormal), the record divides the result into three
subfields with the component delimiter inserted
between subfields: >500 mg/g ABNORMAL.
• For Clinitek Advantus microscopic data results, the
record contains two components.
The first component contains the user entered data,
and the second the configured units for the entry, as in
the following example:
45.4 /uL
If no units for the selected microscopic data exist, the
analyzer sends an empty component:
45.5
7. Clinical result
level
The level of the result with respect to the total number of
reportable clinical result levels for the test.
A level of 1 is assigned to the lowest test value. For
example, a chemistry test may have five result levels as in
the following list:
• NEGATIVE
• TRACE
• 30 mg/dL
• 100 mg/dL
• ≥300 mg/dL
Because the value of 100 mg/dL is the 4th result level, the
value assigned to the Clinical Result Level field is 4.
For Clinitek Advantus microscopic data results, the value
is always 1.
04826807 Rev. A
Examples of Results Records
Clinitek Advantus and Clinitek 500 analyzers:
R | 1 | N | PRO | 6 | 100 ^ mg/dL | 4 | 0 | A <CR>
Clinitek Advantus analyzer:
R | 2 | N | RBC | 100 | 55000 ^ /uL | 1 | 0 | M <CR>
Test Strip Assays and Abbreviations
The following tables display the available tests for the supported test strips.
•Table 3-14 displays the tests supported on the Clinitek Advantus and Clinitek 500 analyzers.
It also displays the abbreviations and the numeric ID for each test.
•Table 3-15 displays the microscopic data tests supported on the Clinitek Advantus analyzers.
The numeric value for each test provides a non-language dependent identifier for later data
analysis.
8. Altered decode
status
The state of decodes on the analyze:
• If the analyzer does not use altered decodes, this field
contains a 0.
• If the analyzer does use altered decodes, this field
contains a 1.
• For Clinitek Advantus microscopic data results, this
field always contains a 1.
9. Result origin The source of the test result:
• If the analyzer calculates the result, the value is A.
• If the result is entered manually, the value is M.
• If the result is edited, the value is E.
For Clinical Results, this is the last field in the record.
• For Clinitek Advantus microscopic data results, the
value is always M because the result is entered
manually.
10. Auxiliary test
information
Not used for Clinical Result records.
These are result records in a Patient Record with a value of
‘C’ in the Results Format field.
04826807 Rev. A
Table 3-14 Test Strip Assays and Abbreviations
The following table contains microscopic data test and numeric IDs for results on the Clinitek
Advantus analyzer:
Table 3-15 Microscopic Data Results
Test Abbreviation Numeric ID
Glucose GLU 1
Bilirubin BIL 2
Ketone KET 3
Specific Gravity SG 4
pH pH 5
Protein PRO 6
Urobilinogen URO 7
Nitrite NIT 8
Occult Blood BLO 9
Leukocytes LEU 10
Color --- 11
Clarity --- 12
Creatinine CRE 13
Protein to Creatinine Ratio P:C 14
Albumin ALB 15
Albumin to Creatinine Ratio A:C 16
Microscopic Data Numeric ID Microscopic Data Numeric ID
RBC /uL 100 PATH CASTS 115
RBC /HPF 101 PATH CASTS /HPF 116
RBC /LPF 102 PATH CASTS /LPF 117
WBC /uL 103 CYSTALS 118
WBC /HPF 104 CYSTALS /HPF 119
WBC /LPF 105 CYSTALS /LPF 120
EC /uL 106 YEAST 121
EC /HPF 107 YEAST /HPF 122
EC /LPF 108 YEAST /LPF 123
BACT /uL 109 SPERM 124
BACT /HPF 110 SRC 125
BACT /LPF 111 OTHER 126
CASTS /uL 112 TOTAL COUNT 127
CASTS /HPF 113 Custom data 128
CASTS /LPF 114
3-18 Clinitek Advantus and Clinitek 500 Interface Specification: Formatting Test Records
086D0001-01, Rev. A
04826807 Rev. A
Appendix A: Safety Instructions

This information summarizes the established guidelines for handling laboratory biohazards.
This summary is based on the guidelines developed by the Centers for Disease Control, the
Clinical and Laboratory Standards Institute Document M29-A3, Protection of Laboratory
Workers from Occupationally Acquired Infections, and the Occupational Safety and Health
Administration’s Bloodborne Pathogens Standard.1–3
Protecting Yourself from Biohazards
Use this summary for general information only. It is not intended to replace or supplement your
laboratory or hospital biohazard control procedures.
By definition, a biohazardous condition is a situation involving infectious agents biological in
nature, such as the hepatitis B virus, the human immunodeficiency virus, and the tuberculosis
bacterium. These infectious agents may be present in human blood and blood products and in
other body fluids.
The following are the major sources of contamination when handling potentially infectious
agents:
•needlesticks
•hand-to-mouth contact
•hand-to-eye contact
•direct contact with superficial cuts, open wounds, and other skin conditions that may permit
absorption into subcutaneous skin layers
•splashes or aerosol contact with skin and eyes
A–2 CLINITEK Advantus and CLINITEK 500 Interface Specification: Safety Instructions
04826807 Rev. A
To prevent accidental contamination in a clinical laboratory, strictly adhere to the following
procedures:
•Wear gloves while servicing parts of the instrument that have contact with body fluids such as
serum, plasma, urine, or whole blood.
•Wash your hands before going from a contaminated area to a noncontaminated area, or when
you remove or change gloves.
•Perform procedures carefully to minimize aerosol formation.
•Wear facial protection when splatter or aerosol formation are possible.
•Wear personal protective equipment such as safety glasses, gloves, lab coats or aprons when
working with possible biohazard contaminants.
•Keep your hands away from your face.
•Cover all superficial cuts and wounds before starting any work.
•Dispose of contaminated materials according to your laboratory’s biohazard control
procedures.
•Keep your work area disinfected.
•Disinfect tools and other items that have been near any part of the instrument sample path or
waste area with 10% v/v bleach.
•Do not eat, drink, smoke, or apply cosmetics or contact lenses while in the laboratory.
•Do not mouth pipet any liquid, including water.
•Do not place tools or any other items in your mouth.
•Do not use the biohazard sink for personal cleaning such as rinsing coffee cups or washing
hands.
To prevent needlestick injuries, needles should not be recapped, purposely bent, cut, broken,
removed from disposable syringes, or otherwise manipulated by hand.
References
1. Centers for Disease Control. 1988. Update: Universal precautions for
prevention of transmission of human immunodeficiency virus, hepatitis B
virus and other bloodborne pathogens in healthcare settings. MMWR,
37:377–382, 387, 388.
2. Clinical and Laboratory Standards Institute (formerly NCCLS). Protection of
Laboratory Workers from Occupationally Acquired Infections; Approved
Guideline - Third Edition. CLSI Document M29-A3.[ISBN 1-56238-567-4].
Clinical and Laboratory Standards Institute, 940 West Valley Road, Suite
1400, Wayne, Pennsylvania 19087-1898 USA, 2005).
3. Federal Occupational Safety and Health Administration. Bloodborne
Pathogens Standard. 29 CFR 1910. 1030.
04826807 Rev. A
Appendix B: Service, Ordering, and

Warranty
This section provides the following information:
•address of the Siemens Medical Solutions Diagnostics authorized representative, which is the
Siemens contact within the European community
•addresses for obtaining service and technical information and for ordering supplies
•system warranty and service delivery policy information
Siemens Authorized Representative
Siemens Medical Solutions Diagnostics Europe Limited
Chapel Lane, Swords, Co. Dublin, Ireland
Limited Instrument Warranty and Service Delivery
Policy
Siemens and its authorized distributors may provide customers who acquire new Siemens
instruments with a limited warranty either in a specific agreement or in standard language on
their invoices. This limited warranty is designed to protect customers from the cost associated
with repairing instruments that exhibit malfunctions due to defects in materials and/or
workmanship during the warranty period.
Siemens, at its election, provides warranty service either by providing repair service of the
instrument on site, or by exchanging the defective instrument or component, subject to the
limitations and exclusions set forth in Replacement of Parts and Warranty and Service
Exclusions below. Repairs, replacements or exchanges of instruments or components provided
during the warranty or any additional service period, does not extend the warranty or service
period beyond the initially agreed upon period.
When the customer calls for service, the Siemens representative or authorized distributor
informs the customer of the type of service available for the customer’s instrument, and
instructs the customer as to how to obtain that service.
Warranty Period
The limited warranty period generally commences upon installation of the original instrument at
the customer’s location and extends for a period of 1 year thereafter, unless otherwise
specifically agreed to by and between Siemens (or its authorized distributors) and customer in a
writing signed by duly authorized representatives of both parties (sales representatives are
generally not authorized representatives of Siemens for these purposes).
B–2 Clinitek Advantus and Clinitek 500 Interface Specification: Service, Ordering, and Warranty
04826807 Rev. A
Additional Service Period
The customers, with some exceptions, may purchase additional service coverage beyond any
initial warranty period as part of the original instrument acquisition for second or subsequent
years beyond the original installation date. The customer’s original Purchase Invoice or
appropriate Agreement Addendum must indicate the term in months for additional service
coverage.
Service During Normal Hours
The customer may obtain service for instruments during normal business hours by contacting
the nearest Siemens location or authorized distributor. Refer to the list of Siemens locations in
this section.
Extent of a Service Call
Warranty or service calls generally include onsite repair or exchange of instruments or
components, travel to the location of the instrument, and onsite labor during normal business
hours. A warranty or service call is initiated by the customer by following the instructions on
how to obtain service for the customer’s instrument. The service call is considered complete
when any defects in material or workmanship have been corrected by repair or replacement and
the instrument conforms to the applicable specifications. When service is complete, the
customer receives a copy of the documentation detailing all work performed by the Siemens
representative or authorized distributor.
Service Outside Normal Hours
Customers, with some exceptions, may also request service to be delivered or an exchange to be
initiated outside normal business hours, including evenings, weekend days, or nationally
observed holidays, by contacting the nearest Siemens location or authorized distributor. Service
performed outside normal hours is subject to a surcharge unless the customer has in place a
service product option that provides service at the time requested.
Replacement of Parts
In performing service, Siemens or its authorized distributors provide appropriate parts to repair
the instrument, or arranges for the exchange of the instrument or affected parts, at no charge
with the exception of certain parts or subassemblies that are considered Customer Maintenance
Items. Customer Maintenance Items include, but are not limited to, the following items: lamps,
electrodes or sensors (which are covered by a separate warranty), reagents, calibrators, controls,
paper, and pens. Consult the appropriate system operator’s manuals for a complete list of
Customer Maintenance Items for any specific model of instrument.
Clinitek Advantus and Clinitek 500 Interface Specification: Service, Ordering, and Warranty B–3
04826807 Rev. A
Design Changes and Retrofitting of Instruments
Siemens reserves the right to change the design or construction of specific models of
instruments at any time without incurring any obligation to make such changes available to
individual customers or instruments. If Siemens notifies customers of a change that improves
the performance or reliability of their instrument, and requests to retrofit that instrument, the
customer must agree to allow Siemens or an authorized distributor, at Siemens’ expense, to
retrofit components or make design changes, which does not adversely affect the instrument’s
performance characteristics.
Key Operator Designation
Each customer designates a key operator who is available to Siemens representatives to describe
instrument malfunctions by telephone and/or to perform simple adjustments and corrections as
requested. If a key operator is not designated or is unavailable when the customer requests
service, the delivery of service may be delayed.
OSHA Requirements (US only)
When service is required at a customer location, the customer must provide the Siemens
representative with adequate facilities that comply with the regulations of the Secretary of Labor
under the Occupational Safety and Health Act (OSHA) of 1970, as amended.
Warranty and Service Exclusions
The following exclusions are in addition to any exclusions provided for in any written warranty
or service agreement.
IF ANY OF THE FOLLOWING EVENTS OCCUR, THE WARRANTY OR SERVICE
PROVISIONS DO NOT APPLY:
1. Repairs or modifications have been made to the instrument by someone other
than an authorized Siemens representative.
2. The instrument has been operated using accessories and supplies other than
Siemens brand accessories, or consumable supplies and/or reagents not
having the same grade, quality, and composition as defined in the system
operator’s manuals.
3. Siemens has notified customers of a change that improves the performance or
reliability of their instrument and customer has not agreed to retrofit or make
design changes to the instrument.
4. Customer did not purchase the instrument from Siemens or one of its
authorized distributors.
5. The instrument has not been installed within 90 days of shipment to the
customer’s facility unless otherwise specified.
04826807 Rev. A
6. The customer has not performed appropriate customer maintenance
procedures, as outlined in the system operator’s manuals.
7. The instrument has been misused or used for a purpose for which it was not
intended.
8. The instrument has been damaged in transit to the customer or damaged by
the customer while moving or relocating it without supervision by a Siemens
representative.
9. Damage was caused by floods, earthquakes, tornados, hurricanes, or other
natural or man-made disasters.
10. Damage was caused by Acts of War, vandalism, sabotage, arson, or civil
commotion.
11. Damage was caused by electrical surges or voltages exceeding the tolerances
outlined in the system operator’s manuals.
12. Damage was caused by water from any source external to the instrument.
13. The customer has purchased an alternative agreement whose terms of
warranty or service supersede these provisions.
Siemens or its authorized distributors can invoice customers, at current standard labor and parts
rates, for instruments repaired to correct damage or malfunctions due to any of the reasons listed
above.
OTHER THAN AS STATED ABOVE, THERE ARE NO OTHER WARRANTIES, EXPRESS
OR IMPLIED, WITH RESPECT TO THE INSTRUMENT, ITS SALE TO THE CUSTOMER,
ITS LEASE TO THE CUSTOMER, OR THE SALE OF THE INSTRUMENT TO THE
CUSTOMER AT THE EXPIRATION OR TERMINATION OF THE LEASE AGREEMENT.
SIEMENS SPECIFICALLY DISCLAIMS ANY AND ALL IMPLIED WARRANTIES OF
MERCHANTABILITY OR FITNESS FOR A PARTICULAR USE OR PURPOSE.
SIEMENSS LIABILITY FOR BREACH OF ANY WARRANTY OR SERVICE
AGREEMENT SHALL BE LIMITED ONLY TO THE REPAIR OR REPLACEMENT OF
DEFECTIVE EQUIPMENT AND SHALL NOT INCLUDE ANY DAMAGES OF ANY
KIND, WHETHER DIRECT, INDIRECT, INCIDENTAL, CONTINGENT, OR
CONSEQUENTIAL. SIEMENS SHALL NOT BE LIABLE FOR DELAY FROM ANY
CAUSE IN PROVIDING REPAIR OR EXCHANGE SERVICE.
ANY LIMITATIONS OR OTHER PROVISIONS NOT CONSISTENT WITH APPLICABLE
LAW IN PARTICULAR JURISDICTIONS OR A SPECIFIC WRITTEN AGREEMENT DO
NOT APPLY TO CUSTOMERS IN THOSE JURISDICTIONS OR SUBJECT TO THOSE
AGREEMENTS.
Clinitek Advantus and Clinitek 500 Interface Specification: Service, Ordering, and Warranty B–5
04826807 Rev. A
Information for Technical Assistance

Refer to the procedures in this appendix to provide system information that you may need when
you call for technical assistance.
Locating the System Serial Number
Remove the test table. The serial number is located on the base plate assembly.
Addresses
For technical assistance contact your local technical support provider. For customer service or
additional information contact your local technical support distributor.
Siemens Medical Solutions Diagnostics
511 Benedict Avenue
Tarrytown, NY 10591
Siemens Medical Solutions Diagnostics Pty Ltd
ABN 65 007 436 651
885 Mountain Highway
Bayswater Victoria 3153
Australia
Clinitek AdvantusClinitek 500
04826807 Rev. A
04826807 Rev. A
Appendix C: Result Unit Tables

English and Chinese Conventional Units
Table C-1 English and Chinese – Conventional
Test Abbreviation Normal Plus System
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIVE NEGATIVE
Multistix Family of Test
Strips
TRACE
30 mg/dL
100 mg/dL
>=300 mg/dL
TRACE
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
Clinitek Microalbumin 9
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
LOW
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
NIT NEGATIVE No change
POSITIVE
GLU NEGATIVE NEGATIVE
Multistix and Multistix
PRO Families of Test
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
TRACE
1+
2+
3+
C–2 Clinitek Advantus and Clinitek 500 Interface Specification: Result Unit Tables
04826807 Rev. A
Clinitek Microalbumin 9 100 mg/dL
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
TRACE
1+
2+
3+
4+
KET NEGATIVE NEGATIVE
TRACE
15 mg/dL
40 mg/dL
>=80 mg/dL
TRACE
1+
2+
3+
BIL NEGATIVE NEGATIVE
SMALL
MODERATE
LARGE
1+
2+
3+
BLO NEGATIVE NEGATIVE
TRACE-LYSED
TRACE-INTACT
SMALL
MODERATE
LARGE
TRACE-LYSED
TRACE-INTACT
1+
2+
3+
URO 0.2 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
LEU NEGATIVE NEGATIVE
TRACE
SMALL
MODERATE
LARGE
TRACE
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
Clinitek Advantus and Clinitek 500 Interface Specification: Result Unit Tables C–3
04826807 Rev. A
A:C
Strips
.
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
A:C
NORMAL DILUTE
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL DILUTE No change
NORMAL
150 mg/g
ABNORMAL
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
NORMAL
300 mg/g
ABNORMAL
1500 mg/g
ABNORMAL
3000 mg/g
ABNORMAL
>=5000 mg/g
ABNORMAL
04826807 Rev. A
COL
If color is “determined by
the Tech”, an additional
option of OTHER is
available.
LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
No change
CLA CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
No change
04826807 Rev. A
English and Chinese S.I. Units
Table C-2 English and Chinese – S.I. Units
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO
Strips
NEGATIVE
TRACE
0.3 g/L
1.0 g/L
>=3.0 g/L
NEGATIVE
TRACE
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
LOW
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIVE
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
TRACE
1+
2+
3+
04826807 Rev. A
Clinitek Microalbumin 9 5.5 mmol/L
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
TRACE
1+
2+
3+
4+
TRACE
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
TRACE
1+
2+
3+
BIL NEGATIVE NEGATIVE
SMALL
MODERATE
LARGE
1+
2+
3+
BLD NEGATIVE NEGATIVE
TRACE-LYSED
TRACE-INTACT
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
TRACE-LYSED
TRACE-INTACT
1+
2+
3+
UBG 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
TRACE
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
HIGH ABNORMAL
A:C
NORMAL DILUTE
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
HIGH ABNORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ABNORMAL
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:C
NORMAL
33.9 mg/mmol
ABNORMAL
170 mg/mmol
ABNORMAL
339 mg/mmol
ABNORMAL
>=566 mg/mmol
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
No change
CLA CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
No change
04826807 Rev. A
English Nordic Units
Table C-3 English Nordic – Nordic Plus System
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Multistix Family of Test Strips +/-
1+
2+
3+
TRACE
1+
2+
3+
PRO NEGATIVE No change
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
LOW
1+
2+
3+
PRO NEGATIVE No change
Multistix PRO 6B
Multistix PRO 6K
1+
2+
3+
POSITIVE
Strips
1+
2+
3+
4+
TRACE
1+
2+
3+
04826807 Rev. A
Clinitek Microalbumin 9 1+
2+
3+
4+
5+
TRACE
1+
2+
3+
4+
1+
2+
3+
4+
TRACE
1+
2+
3+
BIL NEGATIVE No change
1+
2+
3+
BLD NEGATIVE No change
+/-
+/-INTACT
1+
2+
3+
UBG 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
1+
2+
3+
4+
TRACE
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
HIGH ABNORMAL
A:C
NORMAL DILUTE
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
HIGH ABNORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ABNORMAL
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:C
NORMAL
33.9 mg/mmol
ABNORMAL
170 mg/mmol
ABNORMAL
339 mg/mmol
ABNORMAL
>=566 mg/mmol
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
No change
CLA CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
No change
04826807 Rev. A
French Conventional Units
Table C-4 Français, unités conventionnelles
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIF NEGATIF
Strips
TRACES
0.3 g/L
1.0 g/L
>=3.0 g/L
TRACES
1+
2+
3+
PRO NEGATIF NEGATIF
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
FAIBLE
1+
2+
3+
PRO NEGATIF NEGATIF
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
NIT NEGATIF No change
POSITIF
GLU NEGATIF NEGATIF
Strips
TRACES
2.5 g/L
5.0 g/L
>=10.0 g/L
TRACES
1+
2+
3+
04826807 Rev. A
GLU NEGATIF NEGATIF
Clinitek Microalbumin 9 TRACES
2.5 g/L
5.0 g/L
10 g/L
>=20 g/L
TRACES
1+
2+
3+
4+
CET NEGATIF NEGATIF
TRACES
0.15 g/L
0.4 g/L
>=0.8 g/L
TRACES
1+
2+
3+
BIL NEGATIF NEGATIF
FAIBLE
MOYEN
FORT
1+
2+
3+
SNG NEGATIF NEGATIF
TRACES-LYSE
TRACES-INTACT
env. 25 GR/uL
env. 80 GR/uL
env. 200 GR/uL
TRACES-LYSE
TRACES-INTACT
1+
2+
3+
URO 0.2 mg/dL
1.0 mg/dL
No change
2.0 mg/dL
4.0 mg/dL
>=8.0 mg/dL
LEU NEGATIF NEGATIF
env. 15 GB/uL
env. 70 GB/uL
env. 125 GB/uL
env. 500 GB/uL
TRACES
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Clinitek Microalbumin
and Multistix PRO
Families of Test Strips
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ANORMAL ELEVE
A:C
NORMAL, DILUEE
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ANORMAL ELEVE
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL, DILUEE No change
NORMAL
150 mg/g
ANORMAL
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
NORMAL DILUEE No change
NORMAL
300 mg/g
ANORMAL
1500 mg/g
ANORMAL
3000 mg/g
ANORMAL
>=5000 mg/g
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CLR. JAUNE
JAUNE
FONC. JAUNE
CLR. ORANGE
ORANGE
FONC. ORANGE
CLR. ROUGE
ROUGE
FONC. ROUGE
CLR. VERT
VERT
FONC. VERT
CLR. BLEU
BLEU
FONC. BLEU
CLR. MARRON
MARRON
FONC. MARRON
No change
ASP LIMPIDE
LEG. TROUBLE
TROUBLE
OPAQUE
AUTRE
No change
04826807 Rev. A
French S. I. Units
Table C-5 Français, unités internationales (SI)
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIF NEGATIF
Strips
TRACES
0.3 g/L
1.0 g/L
>=3.0 g/L
TRACES
1+
2+
3+
PRO NEGATIF NEGATIF
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
FAIBLE
1+
2+
3+
PRO NEGATIF NEGATIF
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
NIT NEGATIF No change
POSITIF
GLU NEGATIF NEGATIF
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
TRACES
1+
2+
3+
04826807 Rev. A
GLU NEGATIF NEGATIF
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
TRACES
1+
2+
3+
4+
CET NEGATIF NEGATIF
TRACES
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
TRACES
1+
2+
3+
BIL NEGATIF NEGATIF
FAIBLE
MOYEN
FORT
1+
2+
3+
SNG NEGATIF NEGATIF
TRACES-LYSE
TRACES-INTACT
FAIBLE
MOYEN
FORT
TRACES-LYSE
TRACES-INTACT
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU NEGATIF NEGATIF
TRACES
FAIBLE
MOYEN
FORT
TRACES
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ANORMAL ELEVE
A:C
.
NORMAL, DILUEE
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ANORMAL ELEVE
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL, DILUEE No change
NORMAL
17.0 mg/mmol
ANORMAL
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
NORMAL DILUEE No change
NORMAL
33.9 mg/mmol
ANORMAL
170 mg/mmol
ANORMAL
339 mg/mmol
ANORMAL
>=566 mg/mmol
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CLR.JAUNE
JAUNE
FONC.JAUNE
CLR.ORANGE
ORANGE
FONC.ORANGE
CLR.ROUGE
ROUGE
FONC.ROUGE
CLR.VERT
VERT
FONC.VERT
CLR.BLEU
BLEU
FONC.BLEU
CLR.MARRON
MARRON
FONC.MARRON
No change
ASP LIMPIDE
LEG. TROUBLE
TROUBLE
OPAQUE
AUTRE
No change
04826807 Rev. A
German Conventional Units
Table C-6 Deutsch, Einheiten: Konventionell
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIV NEGATIV
Strips
SPUR
30 mg/dL
100 mg/dL
>=300 mg/dL
SPUR
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
WENIG
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
NIT NEGATIV No change
POSITIV
GLU NEGATIV NEGATIV
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
SPUR
1+
2+
3+
04826807 Rev. A
GLU NEGATIV NEGATIV
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
SPUR
1+
2+
3+
4+
KET NEGATIV NEGATIV
SPUR
15 mg/dL
40 mg/dL
>=80 mg/dL
SPUR
1+
2+
3+
BIL NEGATIV NEGATIV
SCHWACH
MAESSIG
STARK
1+
2+
3+
OBL 0 Ery/uL NEGATIV
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
SPUR-LYSE
SPUR-ZELLEN
1+
2+
3+
UBG 0.2 mg/dL
1.0 mg/dL
No change
2.0 mg/dL
4.0 mg/dL
>=8.0 mg/dL
LEU 0 Leu/uL NEGATIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
SPUR
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
KRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:K
Strips
<30 mg/g
NORMAL
No change
30-300 mg/g
ABNORMAL
>300 mg/g
STARK ABNORMAL
A:K
A OK / K GERING
<30 mg/g
NORMAL
No change
30-300 mg/g
ABNORMAL
>300 mg/g
STARK ABNORMAL
P:K
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
P OK / K GERING No change
NORMAL
150 mg/g
ABNORMAL
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:K
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:K
NORMAL
300 mg/g
ABNORMAL
1500 mg/g
ABNORMAL
3000 mg/g
ABNORMAL
>=5000 mg/g
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
HELL GELB
GELB
DUNK.GELB
HELL ORANGE
ORANGE
DUNK.ORANGE
HELL ROT
ROT
DUNK.ROT
HELL GRUEN
GRUEN
DUNK.GRUEN
HELL BLAU
BLAU
DUNK.BLAU
HELL BRAUN
BRAUN
DUNK.BRAUN
No change
CLA KLAR
FLOCKIG
S.♦FLOCKIG
TRUEB
ANDERS
No change
04826807 Rev. A
German S. I. Units
Table C-7 Deutsch, Einheiten: Internationales Einheitensystem (SI)
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIV NEGATIV
Multistix Family of Tests SPUR
0.3 g/L
1.0 g/L
>=3.0 g/L
SPUR
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
WENIG
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIV
GLU NEGATIV NEGATIV
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
SPUR
1+
2+
3+
04826807 Rev. A
GLU NEGATIV NEGATIV
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
SPUR
1+
2+
3+
4+
KET NEGATIV NEGATIV
SPUR
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
SPUR
1+
2+
3+
BIL NEGATIV NEGATIV
SCHWACH
MAESSIG
STARK
1+
2+
3+
OBL 0 Ery/uL NEGATIV
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
SPUR-LYSE
SPUR-ZELLEN
1+
2+
3+
UBG 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU 0 Leu/uL NEGATIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
SPUR
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
KRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:K
Strips
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
STARK ABNORMAL
A:K
A OK / K GERING
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ABNORMAL
>33.9 mg/mmol
STARK ABNORMAL
P:K
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ABNORMAL
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:K
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ABNORMAL
>56.6 mg/mmol
ABNORMAL
P:K
NORMAL
33.9 mg/mmol
ABNORMAL
170 mg/mmol
ABNORMAL
339 mg/mmol
ABNORMAL
>=566 mg/mmol
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
HELL GELB
GELB
DUNK.GELB
HELL ORANGE
ORANGE
DUNK.ORANGE
HELL ROT
ROT
DUNK.ROT
HELL GRUEN
GRUEN
DUNK.GRUEN
HELL BLAU
BLAU
DUNK.BLAU
HELLBRAUN
BRAUN
DUNK.BRAUN
No change
CLA KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
No change
04826807 Rev. A
Italian Conventional Units
Table C-8 Italiano, Unità - Convenzionali
PS <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIVO NEGATIVO
Multistix Family of Tests TRACCE
30 mg/dL
100 mg/dL
>=300 mg/dL
TRACCE
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
BASSO
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
NIT NEGATIVO No change
POSITIVO
GLU NEGATIVO NEGATIVO
Strips
1.0 g/L
2.5 g/L
5.0 g/L
>=10.0 g/L
TRACCE
1+
2+
3+
04826807 Rev. A
Clinitek Microalbumin 9 1.0 g/L
2.5 g/L
5.0 g/L
10.0 g/L
>=20.0 g/L
TRACCE
1+
2+
3+
4+
KET NEGATIVO NEGATIVO
TRACCE
15 mg/dL
40 mg/dL
>=80 mg/dL
TRACCE
1+
2+
3+
BIL NEGATIVO NEGATIVO
LEGGERO
MEDIO
FORTE
1+
2+
3+
SAN NEGATIVO NEGATIVO
TRACCE(LIS.)
TRACCE(INT.)
LEGGERO
MEDIO
FORTE
TRACCE(LIS.)
TRACCE(INT.)
1+
2+
3+
URO 0.2 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
LEU NEGATIVO NEGATIVO
Ca 15 Cel/uL
Ca 70 Cel/uL
Ca 125 Cel/uL
Ca500 Cel/uL
TRACCE
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Strips
<30 mg/g
NORMALE
No change
30-300 mg/g
ANORMALE
>300 mg/g
MOLTO ANORMALE
A:C
URINA DILUITA
<30 mg/g
NORMALE
No change
30-300 mg/g
ANORMALE
>300 mg/g
MOLTO ANORMALE
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
URINA DILUITA No change
NORMALE
150 mg/g
ANORMALE
300 mg/g
ANORMALE
>500 mg/g
ANORMALE
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMALE No change
300 mg/g
ANORMALE
>500 mg/g
ANORMALE
P:C
NORMALE
300 mg/g
ANORMALE
1500 mg/g
ANORMALE
3000 mg/g
ANORMALE
>=5000 mg/
ANORMALE
04826807 Rev. A
COL
option of OTHER is
available.
CHIA.GIALLO
GIALLO
SCUR.GIALLO
CHIA.ARANCIONE
ARANCIONE
SCUR.ARANCIONE
CHIA.ROSSO
ROSSO
SCUR.ROSSO
CHIA.VERDE
VERDE
SCUR.VERDE
CHIA.AZZURRO
AZZURRO
SCUR.AZZURRO
CHIA.MARRONE
MARRONE
SCUR.MARRONE
No change
ASP LIMPIDA
LEG. TORBIDA
TORBIDA
MOL. TORBIDA
ALTRO
04826807 Rev. A
Italian S.I. Units
Table C-9 Italiano, Unità - Internazionali (SI)
PS <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Multistix Family of Tests TRACCE
0.3 g/L
1.0 g/L
>=3.0 g/L
TRACCE
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
BASSO
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIVO
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
TRACCE
1+
2+
3+
04826807 Rev. A
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
TRACCE
1+
2+
3+
4+
KET NEGATIVO NEGATIVO
TRACCE
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
TRACCE
1+
2+
3+
LEGGERO
MEDIO
FORTE
1+
2+
3+
SAN 0 eri/uL NEGATIVO
Ca 10 eri/uL
Ca 10 eri/uL
Ca 25 eri/uL
Ca 80 eri/uL
Ca 200 eri/uL
TRACCE(LIS.)
TRACCE(INT.)
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU 0 Cel/uL NEGATIVO
Ca 15 Cel/uL
Ca 70 Cel/uL
Ca 125 Cel/uL
Ca 500 Cel/uL
TRACCE
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMALE
No change
3.4-33.9 mg/mmol
ANORMALE
>33.9 mg/mmol
MOLTO ANORMALE
A:C
URINA DILUITA
<3.4 mg/mmol
NORMALE
No change
3.4-33.9 mg/mmol
ANORMALE
>33.9 mg/mmol
MOLTO ANORMALE
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMALE
17.0 mg/mmol
ANORMALE
33.9 mg/mmol
ANORMALE
>56.6 mg/mmol
ANORMALE
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMALE No change
33.9 mg/mmol
ANORMALE
>56.6 mg/mmol
ANORMALE
P:C
NORMALE
33.9 mg/mmol
ANORMALE
170 mg/mmol
ANORMALE
339 mg/mmol
ANORMALE
>=566 mg/mmol
ANORMALE
04826807 Rev. A
COL
option of OTHER is
available.
CHIA.GIALLO
GIALLO
SCUR.GIALLO
CHIA.ARANCIONE
ARANCIONE
SCUR.ARANCIONE
CHIA.ROSSO
ROSSO
SCUR.ROSSO
CHIA.VERDE
VERDE
SCUR.VERDE
CHIA.AZZURRO
AZZURRO
SCUR.AZZURRO
CHIA.MARRONE
MARRONE
SCUR.MARRONE
No change
ASP LIMPIDA
LEG. TORBIDA
TORBIDA
MOL. TORBIDA
ALTRO
04826807 Rev. A
Japanese Conventional Units
Table C-17 日本語、単位 - 慣用単位(Japanese)
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO - -
Strips
+/-
30 mg/dL
100 mg/dL
>=300 mg/dL
+/-
1+
2+
3+
PRO - -
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
LOW
1+
2+
3+
PRO - -
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
NIT - No change
+
GLU - -
Strips
0.1 g/dL
0.25 g/dL
0.5 g/dL
>=1.0 g/dL
+/-
1+
2+
3+
04826807 Rev. A
GLU - -
Clinitek Microalbumin 9 0.1 g/dL
0.25 g/dL
0.5 g/dL
1.0 g/dL
>=2.0 g/dL
+/-
1+
2+
3+
4+
KET - No change
+/-
1+
2+
3+
BIL - No change
1+
2+
3+
OB - No change
+/-LYSED
+/-INTACT
1+
2+
3+
URO 0.1 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
WBC - No change
+/-
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Strips
.
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
A:C
NORMAL DILUTE
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
150 mg/g
ABNORMAL
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
NORMAL
300 mg/g
ABNORMAL
1500 mg/g
ABNORMAL
3000 mg/g
ABNORMAL
>=5000 mg/g
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
No change
CLA -
+/-
1+
2+
OTHER
No change
04826807 Rev. A
Japanese JCCLS Units
Table C-18日本語、単位 - JCCLS (Japanese)
SG <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO - -
Strips
+/-
30 mg/dL
100 mg/dL
>=300 mg/dL
+/-
1+
2+
3+
PRO - -
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
LOW
1+
2+
3+
PRO - -
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
NIT - No change
+
GLU - -
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
1+
2+
3+
4+
04826807 Rev. A
GLU - -
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
1+
2+
3+
4+
5+
KET - No change
+/-
1+
2+
3+
BIL - No change
1+
2+
3+
OB - No change
+/-LYSED
+/-INTACT
1+
2+
3+
URO 0.1 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
WBC - No change
+/-
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Strips
.
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
A:C
NORMAL DILUTE
<30 mg/g
NORMAL
No change
30–300 mg/g
ABNORMAL
>300 mg/g
HIGH ABNORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
150 mg/g
ABNORMAL
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ABNORMAL
>500 mg/g
ABNORMAL
P:C
NORMAL
300 mg/g
ABNORMAL
1500 mg/g
ABNORMAL
3000 mg/g
ABNORMAL
>=5000 mg/g
ABNORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
No change
Clarity -
+/-
1+
2+
OTHER
No change
04826807 Rev. A
Portuguese Conventional Units
Table C-10 Português, Unidades — Convencionais
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Strips
INDICIO
30 mg/dL
100 mg/dL
>=300 mg/dL
INDICIO
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
BIAXO
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
POSITIVO
GLI NEGATIVO NEGATIVO
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
INDICIO
1+
2+
3+
04826807 Rev. A
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
INDICIO
1+
2+
3+
4+
CET NEGATIVO NEGATIVO
INDICIO
15 mg/dL
40 mg/dL
>=80 mg/dL
INDICIO
1+
2+
3+
PEQUENO
MODERADO
GRANDE
1+
2+
3+
INDICIO-LISADO
INDICIO-INTACTO
PEQUENO
MODERADO
GRANDE
INDICIO-LISADO
INDICIO-INTACTO
1+
2+
3+
URO 0.2 mg/dL
1.0 mg/dL
No change
2.0 mg/dL
4.0 mg/dL
>=8.0 mg/dL
INDICIO
PEQUENO
MODERADO
GRANDE
INDICIO
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Strips
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ANORMAL ALTO
A:C
DILUIDO NORMAL
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ANORMAL ALTO
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
DILUIDO NORMAL No change
NORMAL
150 mg/g
ANORMAL
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
NORMAL
300 mg/g
ANORMAL
1500 mg/g
ANORMAL
3000 mg/g
ANORMAL
>=5000 mg/g
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CL.AMARELO
AMARELO
OSC.AMARELO
CL.LARANJA
LARANJA
OSC.LARANJA
CL.VERMELHO
VERMELHO
OSC.VERMELH
CL.VERDE
VERDE
OSC.VERDE
CL.AZUL
AZUL
OSC.AZUL
CL.MARRON
MARROM
OSC.MARROM
No change
ASP CLARO
POUCO NEBULOSO
NEBULOSO
TURVO
OUTROS
No change
04826807 Rev. A
Portuguese S.I. Units
Table C-11 Português, Unidades — Internacionais (SI)
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Multistix Family of Tests INDICIO
0.3 g/L
1.0 g/L
>=3.0 g/L
INDICIO
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
BIAXO
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIVO
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
INDICIO
1+
2+
3+
04826807 Rev. A
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
INDICIO
1+
2+
3+
4+
INDICIO
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
INDICIO
1+
2+
3+
PEQUENO
MODERADO
GRANDE
1+
2+
3+
INDICIO-LISADO
INDICIO-INTACTO
PEQUENO
MODERADO
GRANDE
INDICIO-LISADO
INDICIO-INTACTO
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
INDICIO
PEQUENO
MODERADO
GRANDE
INDICIO
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ANORMAL ALTO
A:C
DILUIDO NORMAL
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ANORMAL ALTO
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ANORMAL
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
NORMAL
33.9 mg/mmol
ANORMAL
170 mg/mmol
ANORMAL
339 mg/mmol
ANORMAL
>=566 mg/mmol
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CL.AMARELO
AMARELO
OSC.AMARELO
CL.LARANJA
LARANJA
OSC.LARANJA
CL.VERMELHO
VERMELHO
OSC.VERMELH
CL.VERDE
VERDE
OSC.VERDE
CL.AZUL
AZUL
OSC.AZUL
CL.MARRON
MARROM
OSC.MARROM
No change
ASP CLARO
POUCO NEBULOSO
NEBULOSO
TURVO
OUTROS
No change
04826807 Rev. A
Spanish Conventional Units
Table C-12 Español, Unidades: convencionales
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Multistix Family of Tests INDICIOS
30 mg/dL
100 mg/dL
>=300 mg/dL
INDICIOS
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
BAJO
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
POSITIVO
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
INDICIOS
1+
2+
3+
04826807 Rev. A
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
INDICIOS
1+
2+
3+
4+
INDICIOS
15 mg/dL
40 mg/dL
>=80 mg/dL
INDICIOS
1+
2+
3+
BAJO
MODERADO
ALTO
1+
2+
3+
IND.HEMOLIZ.
IND.INTACTOS
Apr 25 Hem/uL
Apr 80 Hem/uL
Apr 200 Hem/uL
IND.HEMOLIZ.
IND.INTACTOS
1+
2+
3+
URO 0.2 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
Apr 15 Leu/uL
Apr 70 Leu/uL
Apr 125 Leu/uL
Apr 500 Leu/uL
INDICIOS
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:C
Strips
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ALTAMENTE ANORMAL
A:C
DILUIDO NORMAL
<30 mg/g
NORMAL
No change
30-300 mg/g
ANORMAL
>300 mg/g
ALTAMENTE ANORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
150 mg/g
ANORMAL
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ANORMAL
>500 mg/g
ANORMAL
P:C
NORMAL
300 mg/g
ANORMAL
1500 mg/g
ANORMAL
3000 mg/g
ANORMAL
>=5000 mg/g
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CL.AMARILLO
AMARILLO
OSC.AMARILLO
CL.ANARANJAD
ANARANJAD
OSC.ANARANJAD
CL.ROJO
ROJO
OSC.ROJO
CL.VERDE
VERDE
OSC.VERDE
CL.AZUL
AZUL
OSC.AZUL
CL.MARRON
MARRON
OSC.MARRON
No change
ASP CLARO
LIG.TURBIO
TURBIO
MUY TURBIO
OTROS
04826807 Rev. A
Spanish S.I. Units
Table C-13 Español, Unidades: Internacional (SI)
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
Multistix Family of Tests INDICIOS
0.3 g/L
1.0 g/L
>=3.0 g/L
INDICIOS
1+
2+
3+
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
Bajo
1+
2+
3+
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIVO
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
INDICIOS
1+
2+
3+
04826807 Rev. A
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
INDICIOS
1+
2+
3+
4+
INDICIOS
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
INDICIOS
1+
2+
3+
BAJO
MODERADO
ALTO
1+
2+
3+
SAN 0 Eri/uL NEGATIVO
Apr 10 Eri/uL
Apr 10 Eri/uL
Apr 25 Eri/uL
Apr 80 Eri/uL
Apr 200 Eri/uL
IND.HEMOLIZ.
IND.INTACTOS
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU 0 Leu/uL NEGATIVO
Apr 15 Leu/uL
Apr 70 Leu/uL
Apr 125 Leu/uL
Apr 500 Leu/uL
INDICIOS
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
CRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:C
Strips
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ALTAMENTE ANORMAL
A:C
DILUIDO NORMAL
<3.4 mg/mmol
NORMAL
No change
3.4-33.9 mg/mmol
ANORMAL
>33.9 mg/mmol
ALTAMENTE ANORMAL
P:C
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ANORMAL
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ANORMAL
>56.6 mg/mmol
ANORMAL
P:C
NORMAL
33.9 mg/mmol
ANORMAL
170 mg/mmol
ANORMAL
339 mg/mmol
ANORMAL
>=566 mg/mmol
ANORMAL
04826807 Rev. A
COL
option of OTHER is
available.
CL.AMARILLO
AMARILLO
OSC.AMARILLO
CL.NARANJA
NARANJA
OSC.NARANJA
CL.ROJO
ROJO
OSC.ROJO
CL.VERDE
VERDE
OSC.VERDE
CL.AZUL
AZUL
OSC.AZUL
CL.MARRON
MARRON
OSC.MARRON
No change
ASP CLARO
LIG.TURBIO
TURBIO
MUY TURBIO
OTROS
No change
04826807 Rev. A
Swedish Conventional Units
Table C-14 Engelsk og kinesisk, enheder - konventionelle
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIV NEGATIV
Strips
SPAAR
30 mg/dL
100 mg/dL
>=300 mg/dL
SPAAR
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
LAAG
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 6B
Multistix PRO 6K
30 mg/dL
100 mg/dL
300 mg/dL
1+
2+
3+
POSITIV
GLU NEGATIV NEGATIV
Strips
100 mg/dL
250 mg/dL
500 mg/dL
>=1000 mg/dL
SPAAR
1+
2+
3+
04826807 Rev. A
GLU NEGATIV NEGATIV
250 mg/dL
500 mg/dL
1000 mg/dL
>=2000 mg/dL
SPAAR
1+
2+
3+
4+
KET NEGATIV NEGATIV
SPAAR
15 mg/dL
40 mg/dL
>=80 mg/dL
SPAAR
1+
2+
3+
BIL NEGATIV NEGATIV
LITEN
LAGOM
STOR
1+
2+
3+
BLO NEGATIV NEGATIV
SPAAR-LYSERAD
SPAAR-INTAKT
LITEN
LAGOM
STOR
SPAAR-LYSERAD
SPAAR-INTAKT
1+
2+
3+
URO 0.2 E.U./dL
1.0 E.U./dL
No change
2.0 E.U./dL
4.0 E.U./dL
>=8.0 E.U./dL
LEU NEGATIV NEGATIV
SPAAR
LITEN
LAGOM
STOR
SPAAR
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
KRE 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
No change
04826807 Rev. A
A:K
Strips
.
<30 mg/g
NORMAL
No change
30–300 mg/g
ONORMAL
>300 mg/g
HOEG ONORMAL
A:K
NORMAL SPAEDNING
<30 mg/g
NORMAL
No change
30–300 mg/g
ONORMAL
>300 mg/g
HOEG ONORMAL
P:K
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL SPAEDNING No change
NORMAL
150 mg/g
ONORMAL
300 mg/g
ONORMAL
>500 mg/g
ONORMAL
P:K
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
300 mg/g
ONORMAL
>500 mg/g
ONORMAL
P:K
NORMAL
300 mg/g
ONORMAL
1500 mg/g
ONORMAL
3000 mg/g
ONORMAL
>=5000 mg/g
ONORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT.GUL
GUL
DK.GUL
LT.ORANGE
ORANGE
DK.ORANGE
LT.ROED
ROED
DK.ROED
LT.GROEN
GROEN
DK.GROEN
LT.BLAA
BLAA
DK.BLAA
LT.BRUN
BRUN
DK.BRUN
No change
CLA KLAR
ANINGEN OKLAR
OKLAR
GRUMLIG
ANNAT
No change
04826807 Rev. A
Swedish S.I. Units Table C-15 Engelsk og kinesisk, Enheder - Internationale (SI)
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO
Strips
NEGATIV
SPAAR
0.3 g/L
1.0 g/L
>=3.0 g/L
NEGATIV
SPAAR
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
LAAG
1+
2+
3+
PRO NEGATIV NEGATIV
Multistix PRO 6B
Multistix PRO 6K
0.3 g/L
1.0 g/L
3.0 g/L
1+
2+
3+
POSITIV
GLU NEGATIV NEGATIV
Strips
5.5 mmol/L
14 mmol/L
28 mmol/L
>=55 mmol/L
SPAAR
1+
2+
3+
04826807 Rev. A
GLU NEGATIV NEGATIV
14 mmol/L
28 mmol/L
55 mmol/L
>=110 mmol/L
SPAAR
1+
2+
3+
4+
KET NEGATIV NEGATIV
SPAAR
1.5 mmol/L
3.9 mmol/L
>=7.8 mmol/L
SPAAR
1+
2+
3+
BIL NEGATIV NEGATIV
LITEN
LAGOM
STOR
1+
2+
3+
BLD NEGATIV NEGATIV
SPAAR-LYSERAD
SPAAR-INTAKT
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
SPAAR-LYSERAD
SPAAR-INTAKT
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU NEGATIV NEGATIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
SPAAR
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
KRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:K
Strips
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ONORMAL
>33.9 mg/mmol
HOEG ONORMAL
A:K
NORMAL SPAEDNING
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ONORMAL
>33.9 mg/mmol
HOEG ONORMAL
P:K
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ONORMAL
33.9 mg/mmol
ONORMAL
>56.6 mg/mmol
ONORMAL
P:K
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ONORMAL
>56.6 mg/mmol
ONORMAL
P:K
NORMAL
33.9 mg/mmol
ONORMAL
170 mg/mmol
ONORMAL
339 mg/mmol
ONORMAL
>=566 mg/mmol
ONORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT.GUL
GUL
DK.GUL
LT.ORANGE
ORANGE
DK.ORANGE
LT.ROED
ROED
DK.ROED
LT.GROEN
GROEN
DK.GROEN
LT.BLAA
BLAA
DK.BLAA
LT.BRUN
BRUN
DK.BRUN
No change
CLA KLAR
ANINGEN OKLAR
OKLAR
GRUMLIG
ANNAT
No change
04826807 Rev. A
Swedish Nordic Units
Table C-16 Engelsk nordisk, enheder - Nordisk Plus systemenheder
DEN <=1.005
1.010
1.015
1.020
1.025
>=1.030
No change
pH 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
>=9.0
No change
PRO NEGATIV NEGATIV
Multistix Family of Test Strips +/-
1+
2+
3+
SPAAR
1+
2+
3+
PRO NEGATIV No change
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
LAAG
1+
2+
3+
PRO NEGATIV No change
Multistix PRO 6B
Multistix PRO 6K
1+
2+
3+
POSITIV
GLU NEGATIV NEGATIV
Strips
1+
2+
3+
4+
SPAAR
1+
2+
3+
04826807 Rev. A
GLU NEGATIV NEGATIV
Clinitek Microalbumin 9 1+
2+
3+
4+
5+
SPAAR
1+
2+
3+
4+
KET NEGATIV NEGATIV
1+
2+
3+
4+
SPAAR
1+
2+
3+
BIL NEGATIV No change
1+
2+
3+
BLD NEGATIV No change
+/-
+/-INTAKT
1+
2+
3+
URO 3.2 umol/L
16 umol/L
No change
33 umol/L
66 umol/L
>=131 umol/L
LEU NEGATIV NEGATIV
1+
2+
3+
4+
SPAAR
1+
2+
3+
ALB 10 mg/L
30 mg/L
80 mg/L
150 mg/L
No change
KRE 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
No change
04826807 Rev. A
A:K
Strips
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ONORMAL
>33.9 mg/mmol
HOEG ONORMAL
A:K
NORMAL SPAEDNING
<3.4 mg/mmol
NORMAL
No change
3.4–33.9 mg/mmol
ONORMAL
>33.9 mg/mmol
HOEG ONORMAL
P:K
Multistix PRO 10LS
Multistix PRO 10LB
Multistix PRO 10SB
Multistix PRO 7G
NORMAL
17.0 mg/mmol
ONORMAL
33.9 mg/mmol
ONORMAL
>56.6 mg/mmol
ONORMAL
P:K
Multistix PRO 6B
Multistix PRO 6K
NORMAL No change
33.9 mg/mmol
ONORMAL
>56.6 mg/mmol
ONORMAL
P:K
NORMAL
33.9 mg/mmol
ONORMAL
170 mg/mmol
ONORMAL
339 mg/mmol
ONORMAL
>=566 mg/mmol
ONORMAL
04826807 Rev. A
COL
option of OTHER is
available.
LT.GUL
GUL
DK.GUL
LT.ORANGE
ORANGE
DK.ORANGE
LT.ROED
ROED
DK.ROED
LT.GROEN
GROEN
DK.GROEN
LT.BLAA
BLAA
DK.BLAA
LT.BRUN
BRUN
DK.BRUN
No change
CLA KLAR
ANINGEN OKLAR
OKLAR
GRUMLIG
ANNAT
No change
04826807 Rev. A
Appendix D: Clinitek 200/200+ Emulation

Mode
This appendix provides the software communication protocol for the Clinitek® 200 and 200+
emulation mode for Clinitek Advantus and Clinitek 500 analyzers.
Data Transfer Characteristics
The operator selectable data parameters for the Clinitek 200+ are shown in Table D-1. The
Clinitek 200+ instrument uses two Stop Bits. Shaded values are the default option settings.
Table D-1 Data Parameters
Output Data
The transmission of test results data from the Clinitek 200+ instrument can be controlled by
either the instrument or by the interfaced laboratory information system (LIS). If the Handshake
option is set to ON, the communication protocol uses software handshaking and the LIS
controls the transmission of data. If the Handshake option is set to OFF, the communication
protocol does not use software handshaking and the instrument controls the transmission of
data.
Data transmission from the instrument can be suspended by a connected LIS in one of two
ways:
•The Handshake option can be set to ON and the hardware handshake line can be used to stop
data flow.
•An XOFF character (<DC3>) can be sent to the instrument to stop data flow. Data flow does
not resume until an XON character (<DC1> or <DC2>) is sent.
Parameter Setting Options (Shaded options are default options)
Computer On Off
Handshake On Off
Checksum On Off
Baud Rate 110 300 600 1200 2400 4800 9600 19200
Character Bits 7 8
Parity Even Odd None
D–2 Clinitek Advantus and Clinitek 500 Interface Specification: Clinitek 200/200+ Emulation Mode
04826807 Rev. A
The Clinitek 200+ always supports the receipt of the control characters shown in Table D-2
regardless of the setting for the Handshake option.
Table D-2 Data Control Characters
When the Handshake option is set to ON, the Clinitek 200+ supports the output control
characters shown in Table D-3.
Table D-3 Data Output Control Characters
Output Data Types
Data output from the Clinitek 200+ consists of two different data types:
•Instrument ID message.
•CLINICAL Results Format data sets.
Control Character Control Function
<CAN> Resets the RS-232 port to its default condition.
<DC1>, <DC2>
(XON)
Enables data transmission.
<DC3> (XOFF) Stops data output, instrument responds to no further input until
an XON is received.
<DC4 > Redirects all instrument internal printer (Clinitek 200+ printer)
messages to the RS-232 port.
Control Character Control Function
<DC1>, <DC2> Prompt character. Send one set of test result data. If an <ENQ>
control character was the last control character received, send
the Instrument ID message instead of a test result data set.
NOTE: If transmission was disabled during a previous data
transmission, the <DC1> or <DC2> serves only as an XON
control character and re-enables data transmission but sends no
data. If transmission had been disabled but no data was being
transmitted at the time, the <DC1> or <DC2> acts as both an
XON and as the prompt character and data is sent.
<ACK> The last test result data set was received and accepted by the
LIS; address the next data set.
<NAK> The last test result data set was not accepted by the LIS; when
the next prompt character (<DC1> or <DC2>) is received,
resend the same data set.
<ENQ> Set a flag to send the Instrument ID Message when the next
prompt character is received is received.
NOTE: This control character is only active when the
instrument is not in RUN mode.
Clinitek Advantus and Clinitek 500 Interface Specification: Clinitek 200/200+ Emulation Mode D–3
04826807 Rev. A
Table D-4 Control Characters Used in Data Sets
Global Formatting for all Data Sets Output to Serial Port
An <STX> is always output as the first character of a data set.
A checksum of all bytes sent between the <STX> and <ETX> is obtained and truncated to 8
bits. The checksum is sent as the ASCII representation of two hexadecimal digits 0 through F,
the most significant four bits first. These two ASCII characters are sent preceding the <ETX>.
An <ETX> is always output as the last character of a data set.
Calculation of Checksum
Example Instrument ID Message with used to represent the SPACE character:
Steps:
1. Determine the ASCII decimal value of each character (including the SPACE
character) between but not including the <STX> and <ETX> control
character.
2. Sum the ASCII values. (3725)
Control Character Definition
<STX> START OF TEXT character (02H, <^B>).
<CR> Represents the carriage return character (0DH, <^M>).
<LF> Represents the line feed character (0AH, <^J>).
Ck1 Upper 4 bits of an 8-bit checksum converted to an ASCII
character "0-9 or A-F".
Ck2 Lower 4 bits of an 8-bit checksum converted to an ASCII
character "0-9 or A-F".
<ETX> END OF TEXT character (03H, <^C>).
Message ASCII Value of Characters
ASCII Sum
of Line
<STX><CR><LF> 13+10 (<STX> is not included) 23
ID14:3709-11-0
0<CR><LF>
73+68+32+49+52+58+51+55+32+48+57+45+49+49+45 +48+48+13+10 882
CT200+3.00A<CR
><LF>
67+84+50+48+48+43+32+32+32+51+4
6+48+48+65+13+10
717
ENGLISH-CONV.<
CR><LF>
69+78+71+76+73+83+72+32+45+32+3
2+67+79+78+86+46+13+10
1042
Multistix10SG<
CR><LF>
77+85+76+84+73+83+84+73+88+32+4
9+48+32+83+71+13+10
1061
FF<ETX> (checksum and ETX are not
included)
3725
04826807 Rev. A
3. Divide the sum of the ASCII values by 256. Discard the quotient. (3725 / 256
= 14 with remainder of 141)
4. Convert the remainder to a hexadecimal value. (141 / 16 = 8 with a remainder
of 13). Hexadecimal equivalent is 8D.
5. That value is the checksum. Insert it into the message packet prior to sending
the <ETX>.
ASCII Decimal Value Equivalent Hexadecimal Value
00
11
22
33
44
55
66
77
88
99
10 A
11 B
12 C
13 D
14 E
15 F
04826807 Rev. A
Instrument ID Message (Serial Output Only)
The instrument ID message is output to the serial port when an <ENQ> (05H) control character
is received followed by a <DC1> or <DC2>. Even though the instrument ID message packet
contains a checksum, the LIS does not have to acknowledge receipt of the packet.
Table D-5 Variable Field Definition
Table D-6 Instrument ID Packet
Table D-7 Format for Language/Units
Table D-8 Format for Test Strip Names for Multistix® Family
Variable Variable Field Definition
Represents the space character
A Represents the time in 24-hour format.
B Represents the date in the active date format. The formats are
MM-DD-YY, DD-MM-YY, and YYMM-DD.
C Represents the software version.
D Represents the active language/unit option
E Represents the active test strip option
Line Line Content
1 <STX><CR><LF>
2 IDAA:AABB-BB-BB<CR><LF>
3 CT200+C.CCC<CR><LF>
4 DDDDDDDDDDDDDDDD<CR><LF>
5 EEEEEEEEEEEEEEEEEEEEEEE<CR><LF>
6 Ck1Ck2<ETX>
ENGLISH-CONV. FRENCH-CONV. ITALIAN
ENGLISH-+/- FRENCH-S.I. SPANISH
ENGLISH-S.I. GERMAN
Multistix10SG HEMACOMBISTIX MultistixPRO7G
Multistix9 URO-HEMACOMBISGL MultistixPRO7PH
Multistix8SG MultistixPRO10LB MultistixPRO6B
Multistix5 MultistixPRO10LS MultistixPRO6K
MultistixSGL MultistixPRO10SB
N-MultistixSGL MultistixPRO10
04826807 Rev. A
Table D-9 Test Strips Supported by the Clinitek 200+
Table D-10 Test Strips Available for Selection on the Clinitek Advantus, but
not supported by the Clinitek 200+
Clinitek Advantus Full Test Name Clinitek 200+ Name as Transmitted
MULTISTIX 10 SG MULTISTIX♦10♦SG
MULTISTIX 5 MULTISTIX♦5
URO-HEMA COMBISTIX SG L URO-HEMACOMBI♦SG♦L
HEMA-COMBISTIX – LONG HEMA-COMBISTIX-LONG
MULTISTIX PRO 10LB MULTISTIX♦PRO♦10LB
MULTISTIX PRO 10LS MULTISTIX♦PRO♦10LS
MULTISTIX PRO 10SB MULTISTIX♦PRO♦10SB
MULTISTIX PRO 10 MULTISTIX♦PRO♦10
MULTISTIX PRO 7G MULTISTIX♦PRO♦7G
MULTISTIX PRO 7PH MULTISTIX♦PRO♦7PH
MULTISTIX PRO 6B MULTISTIX♦PRO♦6B
MULTISTIX PRO 6K MULTISTIX♦PRO♦6K
Clinitek Advantus Full Test Name Clinitek 200+ Name as Transmitted
MULTISTIX SG MULTISTIX♦SG
MULTISTIX SG L MULTISTIX♦SG L
MULTISTIX MULTISTIX
N-MULTISTIX SG N-MULTISTIX♦SG
NEPHROSTIX L NEPHROSTIX♦L
URO-LABSTIX SG URO-LABSTIX♦SG
URO-LABSTIX SG L URO-LABSTIX♦SG♦L
MULTISTIX 9 MULTISTIX♦9
URO-HEMACOMBISTIX URO-HEMACOMBISTIX
URO-LABSTIX URO-LABSTIX
COMBISTIX SG - LONG COMBISTIX♦SG
URISTIX - LONG URISTIX♦-♦LONG
LIFESTIX LIFESTIX
MULTISTIX PRO 11 MULTISTIX♦PRO♦11
04826807 Rev. A
Variable Field Definitions for Test Result Output
The following table lists each variable and its respective definition as used in the format
descriptions for all test result output. For consistency, the same variables are used in the
definitions for both Result Formats, CLINICAL and TEST. The same variables are also used for
serial, internal printer, and all supported external printer outputs.
Table D-11 Variable Field Definitions
Variable Definition
Represents the space character
* Represents the position used for marking a test result as abnormal for serial
output, 80-column printer output, and form printer output. If Identify
Abnormals is set to ON and the test result can be marked abnormal, an
asterisk (*) is placed in this field. If this position is not used for the
abnormal flag, it is filled with the space character.
Represents the position used for marking a test result as abnormal for
internal printer output. If Identify Abnormals is set to ON and the test result
can be marked abnormal, a block character () is placed in this field. If
this position is not used for the abnormal flag, it is filled with the space
character.
Ck1Ck2 Represents the checksum digits of the test results packet.
<CR> Carriage Return control character
<LF> Line Feed control character
<ETX> End of Text control character
<STX> Start of Text control character
A Represents the Sequence Number assigned to the test result.
B Represents the date in the user-selected format. Valid formats are
MM-DD-YY, DD-MM-YY, and YY-MM-DD.
C Represents the Specimen ID. The Specimen ID field can contain a
maximum of 13 characters. Character positions not used are filled with the
space character. The field is left justified.
D Represents the color of the specimen. The translation for the word Color
plus a colon and a space character plus the actual color value always equals
20 characters. Character positions not used are filled with the space
character. The field is left justified.
E Represents the clarity of the specimen. The translation for the word Clarity
plus a colon and a space character plus the actual clarity value always
equals 20 characters. Character positions not used are filled with the space
character. The field is left justified.
F Represents the clinical result for the test pad. The test result contains 12
characters. Character positions not used are filled with the space character.
The field is left justified.
04826807 Rev. A
CLINICAL Results Format Output
Global Formatting Requirements for all CLINICAL Mode Results
While the order of presentation of test pad results is user-selectable, general sample information
is always presented before the actual test results. That is, the Sequence Number assigned to the
test result, the date of the test, the Specimen ID, and the Color and Clarity of the sample are
always reported before the individual test results are reported.
The number of lines of general information reported is dependent upon whether the Specimen
ID option is set to ON or OFF.
For those tests that can be marked as abnormal (positive), an asterisk (*) is used to designate the
clinical result as being outside of the normal range for serial output, 80-column printer output,
and form printer output. For output to the internal printer, the block character () designates the
clinical result as being outside of the normal range of results. For serial output data, the asterisk
is always placed directly to the right of the reagent tag of the abnormal test result. For printed
output data, the asterisk or block character is always placed directly to the left of the reagent tag
of the abnormal test result.
Table D-12 Serial Data Results Formats for General Information
Variable Definition
G Represents the quantitative result for the A:C Ratio. This field is variable in
length and contains only the test result.
H Represents the qualitative result for the A:C Ratio. This field is variable in
length and contains only the test result.
I If the P:C ratio is Normal Dilute or Normal this field displays that value. If
the P:C ratio is Abnormal, this field contains the quantitative result for the
P:C Ratio. This field is variable in length and contains only the test result.
J If the P:C ratio is Abnormal contains the translation for Abnormal;
otherwise this line is not printed (sent).
Line #
Line Content
Specimen ID Set to NO
Line Content
Specimen ID Set to YES
1 <STX><CR><LF> <STX><CR><LF>
2 #A-AAABB-BB-BB<CR><LF> #A-AAABB-BB-BB<CR><LF>
3 ID=CCCCCCCCCCCCC<CR><LF>
4 Color:DDDDDDDDDD<CR><LF>
5 Clarity:EEEEEEEEEE<CR><LF>
04826807 Rev. A
Multistix Family of Test Strips
Test result lines are present only for the test pads on the test strip. If a particular test pad is not
present on the test strip, that test result line is eliminated.
The default order of data output is the order of the reagent test pads on the test strip beginning
with Channel 1. The output order can be rearranged by the operator. The format example uses a
Multistix 10 SG test strip because that test strip supports all the reagent test pads in the Multistix
family of test strips.
The reagent tags used in the data are the tags supported by the language/unit selection.
Serial Output Format
Each line contains 20 characters plus the <CR><LF> control characters.
Table D-13 Multistix Family of Test Strips
NOTE:Lines 3, 4, and 5 are eliminated if the Specimen ID option is set to NO. When the Specimen ID
option is set to YES, but the Color and/or Clarity options are set to NO, the Color value field and/or the
Clarity value field are filled with the space character.
Line # Line Content
1 <STX><CR><LF>
2 #A-AAABB-BB-BB<CR><LF>
6 GLU*FFFFFFFFFFFFFF<CR><LF>
7 BIL*FFFFFFFFFFFFFF<CR><LF>
8 KET*FFFFFFFFFFFFFF<CR><LF>
9 SGFFFFFFFFFFFFFF<CR><LF>
10 BLO*FFFFFFFFFFFFFF<CR><LF>
11 pHFFFFFFFFFFFFFF<CR><LF>
PRO*FFFFFFFFFFFFFF<CR><LF>
12 URO*FFFFFFFFFFFFFF<CR><LF>
13 NIT*FFFFFFFFFFFFFF<CR><LF>
15 LEU*FFFFFFFFFFFFFF<CR><LF>
16 Ck1Ck2<ETX>
04826807 Rev. A
Multistix PRO® Family of Test Strips
Test result lines are present only for the test pads on the test strip. If a particular test pad is not
present on the test strip, that test result line is eliminated.
The default order of data output is the order of the reagent test pads on the test strip beginning
with Channel 1, with the exception of PRO, ALB, CRE and the ratios. PRO, ALB, CRE, A:C,
and P:C are reported in that order after all other test pad results have been reported. The output
order for any of the test pad results can be rearranged by the operator, but the ratio results are
always output last and their order cannot be altered. The format examples do not represent valid
test strips because there is no test strip in this family that supports all the test pads. The
examples use all the possible test pads to illustrate the default order in which the results are
reported.
Test results for the ALB test pad are only reported for Multistix PRO 6B and Multistix PRO 6K
test strips. For the other test strips in the Multistix PRO family, the ALB test pad is used in
determining the clinical result reported for PRO. Likewise, the A:C ratio is only reported for the
Multistix PRO 6B and Multistix PRO 6K test strips.
04826807 Rev. A
Serial Output Format
With the exception of the lines used for reporting ratio results, each line contains 20 characters
plus the <CR><LF> control characters. The lines used for reporting ratio results are variable in
length.
Table D-14 Multistix PRO 10LB, 10LS, 10SB, 10, 7G, 7PH
NOTE:Lines 3, 4, and 5 are eliminated if the Specimen ID option is set to NO. When the
Specimen ID option is set to YES, but the Color and/or Clarity options are set to NO, the Color
value field and/or the Clarity value field are filled with the space character.
NOTE:If the P:C result is Normal or Normal Dilute, there is no quantitative (I) result reported.
The qualitative result (J) is reported in its place.
Line # Line Content
1 <STX><CR><LF>
7 BIL*FFFFFFFFFFFFFF<CR><LF>
9 SGFFFFFFFFFFFFFF<CR><LF>
12 URO*FFFFFFFFFFFFFF<CR><LF>
13 NIT*FFFFFFFFFFFFFF<CR><LF>
14 LEU*FFFFFFFFFFFFFF<CR><LF>
15 PRO*FFFFFFFFFFFFFF<CR><LF>
16 CREFFFFFFFFFFFFFF<CR><LF>
17 P:C*IIIIIIIIIIIII,JJJJJJJJJJJJJJ<CR><LF>
18 Ck1Ck2<ETX>
04826807 Rev. A
Table D-15 Multistix PRO 6B, 6K
NOTE:Lines 3, 4, and 5 are eliminated if the Specimen ID option is set to NO. When the
Specimen ID option is set to YES, but the Color and/or Clarity options are set to NO, the Color
value field and/or the Clarity value field are filled with the space character.
NOTE:If the P:C result is Normal or Normal Dilute, there is no quantitative (I) result
Line # Line Content
1 <STX><CR><LF>
10 PRO*FFFFFFFFFFFFFF<CR><LF>
11 ALBFFFFFFFFFFFFFF<CR><LF>
12 CREFFFFFFFFFFFFFF<CR><LF>
13 A:C*GGGGGGGGGGGGGGGG,HHHHHHHHHHHHHHHHH<CR><LF>
14 P:C*IIIIIIIIIIIII,JJJJJJJJJJJJJJ<CR><LF>
15 Ck1Ck2<ETX>
04826807 Rev. A
Result Value Conversions from Clinitek Advantus and

Clinitek 500 to Clinitek 200
English Conventional with PLUS System set to OFF
Supports Clinitek 200 Program Card A40100
Test
Clinitek Advantus or
500 Clinitek 200
Glucose (GLU) NEGATIVE
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIVE
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
Bilirubin (BIL) NEGATIVE
SMALL
MODERATE
LARGE
NEGATIVE
SMALL
MODERATE
LARGE
Ketone (KET) NEGATIVE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
Specific Gravity (SG) ≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (BLO) NEGATIVE
TRACE-INTACT
TRACE-LYSED
SMALL
MODERATE
LARGE
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) NEGATIVE
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVE
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
Urobilinogen (URO) 0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) NEGATIVE
POSITIVE
NEGATIVE
POSITIVE
Leukocytes (LEU) NEGATIVE
TRACE
SMALL
MODERATE
LARGE
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
04826807 Rev. A
English Conventional with PLUS System set to ON
Test
500 Clinitek 200
TRACE
1+
2+
3+
NEGATIVE
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
1+
2+
3+
NEGATIVE
SMALL
MODERATE
LARGE
TRACE
1+
2+
3+
NEGATIVE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-INTACT
TRACE-LYSED
1+
2+
3+
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACE
1+
2+
3+
NEGATIVE
NEGATIVE
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVE
NEGATIVE
POSITIVE
TRACE
1+
2+
3+
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
04826807 Rev. A
English Nordic with PLUS System set to OFF
Test
500 Clinitek 200
1+
2+
3+
4+
NEGATIVE
TRACE
+
++
+++
1+
2+
3+
NEGATIVE
+
++
+++
1+
2+
3+
4+
NEGATIVE
TRACE
+
++
+++
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
+/- INTACT
+/-
1+
2+
3+
NEGATIVE
TRACE
TRACE
+
++
+++
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
+/-
1+
2+
3+
NEGATIVE
TRACE
+
++
+++
Urobilinogen (UBG) 3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
NORMAL
NORMAL
+
++
+++
POSITIVE
NEGATIVE
POSITIVE
1+
2+
3+
4+
NEGATIVE
TRACE
+
++
+++
04826807 Rev. A
English Nordic with PLUS System set to ON
Supports Clinitek 200 Program Card C40103
Test
500 Clinitek 200
TRACE
1+
2+
3+
NEGATIVE
TRACE
+
++
+++
1+
2+
3+
NEGATIVE
+
++
+++
TRACE
1+
2+
3+
NEGATIVE
TRACE
+
++
+++
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
+/- INTACT
+/-
1+
2+
3+
NEGATIVE
TRACE
TRACE
+
++
+++
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACE
1+
2+
3+
NEGATIVE
TRACE
+
++
+++
Urobilinogen (URO) 3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
NORMAL
NORMAL
+
++
+++
POSITIVE
NEGATIVE
+
TRACE
1+
2+
3+
NEGATIVE
TRACE
+
++
+++
04826807 Rev. A
English S.I. with PLUS System set to OFF
Test
500 Clinitek 200
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIVE
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
SMALL
MODERATE
LARGE
NEGATIVE
SMALL
MODERATE
LARGE
TRACE
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIVE
TRACE
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-INTACT
TRACE-LYSED
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACE
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIVE
TRACE
0.3 g/L
1.0 g/L
≥3.0 g/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
POSITIVE
NEGATIVE
POSITIVE
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
04826807 Rev. A
English S.I. with PLUS System set to ON
Test
500 Clinitek 200
TRACE
1+
2+
3+
NEGATIVE
+
++
++
+++
1+
2+
3+
NEGATIVE
SMALL
MODERATE
LARGE
TRACE
1+
2+
3+
NEGATIVE
++
++
+++
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-INTACT
TRACE-LYSED
1+
2+
3+
NEGATIVE
+++
++
+++
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACE
1+
2+
3+
NEGATIVE
NEGATIVE
+
++
+++
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
POSITIVE
NEGATIVE
+
TRACE
1+
2+
3+
NEGATIVE
++
++
+++
04826807 Rev. A
French Conventional with PLUS System set to OFF
Supports Clinitek 200 Program Card G40100
Test
500 Clinitek 200
Glucose (GLU) NEGATIF
TRACES
2.5 g/L
5.0 g/L
≥10.0 g/L
NEGATIF
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
Bilirubin (BIL) NEGATIF
FAIBLE
MOYEN
FORT
NEGATIF
FAIBLE
MOYEN
FORT
Ketone (CET) NEGATIF
TRACES
0.15 g/L
0.4 g/L
≥0.8 g/L
NEGATIF
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
Specific Gravity (DEN) ≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-INTACT
TRACES-LYSE
env. 25 GR/uL
env. 80 GR/uL
env. 200 GR/uL
NEGATIF
TRACE
TRACE
FAIBLE
MOYEN
FORT
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIF
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
Urobilinogen (URO) 0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) NEGATIF
POSITIF
NEGATIF
POSITIF
Leukocytes (LEU) NEGATIF
env. 15 GB/uL
env. 70 GB/uL
env. 125 GB/uL
env. 500 GB/uL
NEGATIF
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
French Conventional with PLUS System set to ON
Supports Clinitek 200 Program Card G40100
Test
500 Clinitek 200
TRACES
1+
2+
3+
NEGATIF
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
1+
2+
3+
NEGATIF
FAIBLE
MOYEN
FORT
TRACES
1+
2+
3+
NEGATIF
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-INTACT
TRACES-LYSE
1+
2+
3+
NEGATIF
TRACE
TRACE
FAIBLE
MOYEN
FORT
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACES
1+
2+
3+
NEGATIF
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIF
NEGATIF
POSITIF
TRACES
1+
2+
3+
NEGATIF
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
French S.I. with PLUS System set to OFF
Supports Clinitek 200 Program Card H40100
Test
500 Clinitek 200
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIF
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
FAIBLE
MOYEN
FORT
NEGATIF
FAIBLE
MOYEN
FORT
TRACES
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIF
TRACES
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) TRACES-INTACT
TRACES-LYSE
FAIBLE
MOYEN
FORT
NEGATIF
ENV. 10 GR/uL
ENV. 10 GR/uL
ENV. 25 GR/uL
ENV. 80 GR/uL
ENV. 200 GR/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
POSITIF
NEGATIF
POSITIF
TRACES
FAIBLE
MOYEN
FORT
NEGATIF
ENV. 15 LEU/uL
ENV. 70 LEU/uL
ENV. 125 LEU/uL
ENV. 500 LEU/uL
04826807 Rev. A
French S.I. with PLUS System set to ON
Supports Clinitek 200 Program Card H40100
Test
500 Clinitek 200
TRACES
1+
2+
3+
NEGATIF
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
1+
2+
3+
NEGATIF
FAIBLE
MOYEN
FORT
TRACES
1+
2+
3+
NEGATIF
TRACES
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-INTACT
TRACES-LYSE
1+
2+
3+
NEGATIF
ENV. 10 GR/uL
ENV. 10 GR/uL
ENV. 25 GR/uL
ENV. 80 GR/uL
ENV. 200 GR/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACES
1+
2+
3+
NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
POSITIF
NEGATIF
POSITIF
TRACES
1+
2+
3+
NEGATIF
ENV. 15 LEU/uL
ENV. 70 LEU/uL
ENV. 125 LEU/uL
ENV. 500 LEU/uL
04826807 Rev. A
German Conventional with PLUS System set to OFF
Supports Clinitek 200 Program Card F40100
Test
500 Clinitek 200
Glucose (GLU) NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
Bilirubin (BIL) NEGATIV
SCHWACH
MAESSIG
STARK
NEGATIV
SCHWACH
MAESSIG
STARK
Ketone (KET) NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OBL) 0 Ery/uL
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
0 rbc/uL
Ca 10 rbc/uL
Ca 10 rbc/uL
Ca 25 rbc/uL
Ca 80 rbc/uL
Ca 200 rbc/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
Urobilinogen (UBG) 0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
Nitrite (NIT) NEGATIV
POSITIV
NEGATIV
POSITIV
Leukocytes (LEU) 0 Leu/uL
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
0 cells/uL
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
German Conventional with PLUS System set to ON
Supports Clinitek 200 Program Card F40100
Test
500 Clinitek 200
SPUR
1+
2+
3+
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
1+
2+
3+
NEGATIV
SCHWACH
MAESSIG
STARK
SPUR
1+
2+
3+
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OBL) NEGATIV
SPUR-ZELLEN
SPURLYSE
1+
2+
3+
0 rbc/uL
Ca 10 rbc/uL
Ca 10 rbc/uL
Ca 25 rbc/uL
Ca 80 rbc/uL
Ca 200 rbc/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
SPUR
1+
2+
3+
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
POSITIV
NEGATIV
POSITIV
Leukocytes (LEU) NEGATIV
SPUR
1+
2+
3+
0 cells/uL
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
German S.I. with PLUS System set to OFF
Test
500 Clinitek 200
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
SCHWACH
MAESSIG
STARK
NEGATIV
SCHWACH
MAESSIG
STARK
SPUR
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
0 rbc/uL
Ca 10 rbc/uL
Ca 10 rbc/uL
Ca 25 rbc/uL
Ca 80 rbc/uL
Ca 200 rbc/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
SPUR
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
POSITIV
NEGATIV
POSITIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
0 cells/uL
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
German S.I. with PLUS System set to ON
Supports Clinitek 200 Program Card c40104
Test
500 Clinitek 200
SPUR
1+
2+
3+
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
1+
2+
3+
NEGATIV
SCHWACH
MAESSIG
STARK
SPUR
1+
2+
3+
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OBL) NEGATIV
SPUR-ZELLEN
SPUR-LYSE
1+
2+
3+
0 rbc/uL
Ca 10 rbc/uL
Ca 10 rbc/uL
Ca 25 rbc/uL
Ca 80 rbc/uL
Ca 200 rbc/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
SPUR
1+
2+
3+
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
POSITIV
NEGATIV
POSITIV
SPUR
1+
2+
3+
0 cells/uL
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
Italian with PLUS System set to OFF
Supports Clinitek 200 Program Card E40100
Test
500 Clinitek 200
Glucose (GLU) NEGATIVO
1.0 g/L
2.5 g/L
5.0 g/L
≥10.0 g/L
NEGATIVO
0.1 g/dL
0.25 g/dL
0.50 g/dL
≥1.0 g/dL
Bilirubin (BIL) NEGATIVO
LEGGERO
MEDIO
FORTE
NEGATIVO
LEGGERO
MEDIO
FORTE
Ketone (KET) NEGATIVO
TRACCE
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVO
TRACCE
15 mg/dL
40 mg/dL
≥80 mg/dL
Specific Gravity (PS) ≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SAN) NEGATIVO
TRACCE(INT.)
TRACCE(LIS.)
LEGGERO
MEDIO
FORTE
NEGATIVO
TRACCE
TRACCE
LEGGERO
MEDIO
FORTE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) NEGATIVO
TRACCE
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVO
TRACCE
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) NEGATIVO
POSITIVO
NEGATIVO
POSITIVO
Leukocytes (LEU) NEGATIVO
Ca 15 Cel/uL
Ca 70 Cel/uL
Ca 125 Cel/uL
Ca 500 Cel/uL
NEGATIVO
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
Italian with PLUS System set to ON
Supports Clinitek 200 Program Card E40100
Test
500 Clinitek 200
TRACCE
1+
2+
3+
NEGATIVO
0.1 g/dL
0.25 g/dL
0.50 g/dL
≥1.0 g/dL
1+
2+
3+
NEGATIVO
LEGGERO
MEDIO
FORTE
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACCE(INT.)
TRACCE(LIS.)
1+
2+
3+
NEGATIVO
TRACCE
TRACCE
LEGGERO
MEDIO
FORTE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
TRACCE
1+
2+
3+
NEGATIVO
Ca 15 cells/uL
Ca 70 cells/uL
Ca 125 cells/uL
Ca 500 cells/uL
04826807 Rev. A
Japanese Conventional with PLUS System set to OFF
Supports Clinitek 200 Program Card B40101
Test
500 Clinitek 200
Glucose (GLU) -
0.1 g/dL
0.25 g/dL
0.5 g/dL
≥1.0 g/dL
-
0.1 g/dL
0.25 g/dL
0.5 g/dL
≥1.0 g/dL
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-INTACT
+/-LYSED
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) -
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese Conventional with PLUS System set to ON
Test
500 Clinitek 200
Glucose (GLU) -
+/-
1+
2+
3+
-
0.1 g/dL
0.25 g/dL
0.5 g/dL
≥1.0 g/dL
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
Specific Gravity (SG) ≤1.005
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-INTACT
+/-LYSED
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) -
+/-
1+
2+
3+
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese JCCLS with PLUS System set to OFF
Test
500 Clinitek 200
Glucose (GLU) -
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
-
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-LYSED
+/-INTACT
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) -
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese JCCLS with PLUS System set to ON
Test
500 Clinitek 200
Glucose (GLU) -
1+
2+
3+
4+
-
1+
2+
3+
4+
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-LYSED
+/-INTACT
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO) -
+/-
1+
2+
3+
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Spanish with PLUS System set to OFF
Supports Clinitek 200 Program Card D40100
Test
500 Clinitek 200
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
BAJO
MODERADO
ALTO
NEGATIVO
BAJO
MODERADO
ALTO
Ketone (CET) NEGATIVO
INDICIOS
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVO
INDICIOS
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
IND.INTACTOS
IND.HEMOLIZ.
Apr 25 Hem/uL
Apr 80 Hem/uL
Apr 200 Hem/uL
NEGATIVO
Apro 10 ERI/uL
Apro 10 ERI/uL
Apro 25 ERI/uL
Apro 80 ERI/uL
Apro 200 ERI/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
INDICIOS
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVO
INDICIOS
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
Apr 15 Leu/uL
Apr 70 Leu/uL
Apr 125 Leu/uL
Apr 500 Leu/uL
NEGATIVO
Apro 15 cel/uL
Apro 70 cel/uL
Apro 125 cel/uL
Apro 500 cel/uL
04826807 Rev. A
Spanish with PLUS System set to ON
Supports Clinitek 200 Program Card D40100
Test
500 Clinitek 200
INDICIOS
1+
2+
3+
NEGATIVO
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
1+
2+
3+
NEGATIVO
BAJO
MODERADO
ALTO
INDICIOS
1+
2+
3+
NEGATIVO
INDICIOS
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
IND.INTACTOS
IND.HEMOLIZ.
1+
2+
3+
NEGATIVO
Apro 10 ERI/uL
Apro 10 ERI/uL
Apro 25 ERI/uL
Apro 80 ERI/uL
Apro 200 ERI/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
INDICIOS
1+
2+
3+
NEGATIVO
INDICIOS
30 mg/dL
100 mg/dL
≥300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
INDICIOS
1+
2+
3+
NEGATIVO
Apro 15 cel/uL
Apro 70 cel/uL
Apro 125 cel/uL
Apro 500 cel/uL
04826807 Rev. A
Result Value Conversions from Clinitek Advantus and

Clinitek 500 to Clinitek 200+
English Conventional with PLUS System set to OFF
Supports Clinitek 200+ Program A4
Test
500 Clinitek 200+
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIVE
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
SMALL
MODERATE
LARGE
NEGATIVE
SMALL
MODERATE
LARGE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-LYSED
TRACE-INTACT
SMALL
MODERATE
LARGE
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
MULTISTIX Family of Test
Strips
NEGATIVE
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVE
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVE
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVE
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
Urobilinogen (URO)
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT)
NEGATIVE
POSITIVE
NEGATIVE
POSITIVE
Leukocytes (LEU)
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
Albumin (ALB) 10 mg/L
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
Creatinine (CRE) 10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
A:C Ratio (A:C) <30 mg/g NORMAL
30-300 mg/g ABNORMAL
>300 mg/g HIGH
ABNORMAL
<30 mg/g NORMAL
>300 mg/g HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMA
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
Invalid Result Value ERROR ERROR
Color (COL) LT. YELLOW
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
English Conventional with PLUS System set to ON
Supports Clinitek 200+ Program A4
Test
500 Clinitek 200+
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1+
2+
3+
NEGATIVE
1+
2+
3+
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-LYSED
TRACE-INTACT
1+
2+
3+
NEGATIVE
TRACE
TRACE
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
MULTISTIX Family of Test
Strips
NEGATIVE
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
LOW
1+
2+
3+
NEGATIVE
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
1+
2+
3+
NEGATIVE
1+
2+
3+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
04826807 Rev. A
Test
500 Clinitek 200+
POSITIVE
NEGATIVE
POSITIVE
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g NORMAL
>300 mg/g HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
English Nordic with PLUS System set to OFF
Supports Clinitek 200+ “For Finland” Option
Test
500 Clinitek 200+
1+
2+
3+
4+
NEGATIVE
1+
2+
2+
3+
1+
2+
3+
NEGATIVE
1+
2+
3+
1+
2+
3+
4+
NEGATIVE
1+
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (BLD) NEGATIVE
+/-
+/- INTACT
1+
2+
3+
NEGATIVE
1+
1+
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
MULTISTIX Group of Test
Strips
NEGATIVE
+/-
1+
2+
3+
NEGATIVE
NEGATIVE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIVE
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIVE
1+
2+
3+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
NORMAL
NORMAL
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
POSITIVE
NEGATIVE
POSITIVE
1+
2+
3+
4+
NEGATIVE
1+
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
Creatinine (CRE) 0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
A:C Ratio (A:C) < 3.4 mg/mmol NORMAL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
< 3.4 mg/mmol NORMAL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
17.0 mg/mmol ABNORMAL
>56.6 mg/mmol ABNORMAL
NORMAL DILUTE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
English Nordic with PLUS System set to ON
Supports Clinitek 200+ “For Finland” Option
Test
500 Clinitek 200+
TRACE
1+
2+
3+
NEGATIVE
1+
2+
2+
3+
1+
2+
3+
NEGATIVE
1+
2+
3+
TRACE
1+
2+
3+
NEGATIVE
1+
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
+/-
+/- INTACT
1+
2+
3+
NEGATIVE
1+
1+
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVE
TRACE
1+
2+
3+
NEGATIVE
NEGATIVE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
LOW
1+
2+
3+
NEGATIVE
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
1+
2+
3+
NEGATIVE
1+
2+
3+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
NORMAL
NORMAL
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
POSITIVE
NEGATIVE
POSITIVE
TRACE
1+
2+
3+
NEGATIVE
1+
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
NORMAL DILUTE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
English S.I. with PLUS System set to OFF
Supports Clinitek 200+ Program C4
Test
500 Clinitek 200+
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIVE
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
SMALL
MODERATE
LARGE
NEGATIVE
SMALL
MODERATE
LARGE
TRACE
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIVE
TRACE
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-LYSED
TRACE-INTACT
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVE
TRACE
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIVE
TRACE
0.3 g/L
1.0 g/L
≥3.0 g/L
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIVE
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIVE
0.3 g/L
1.0 g/L
3.0 g/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
04826807 Rev. A
Test
500 Clinitek 200+
POSITIVE
NEGATIVE
POSITIVE
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
NEGATIVE
Ca 15 Cells/uL
Ca 70 Cells/uL
Ca 125 Cells/uL
Ca 500 Cells/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
NORMAL DILUTE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
English S.I. with PLUS System set to ON
Supports Clinitek 200+ Program C4
Test
500 Clinitek 200+
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1+
2+
3+
NEGATIVE
1+
2+
3+
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACE-LYSED
TRACE-INTACT
1+
2+
3+
NEGATIVE
TRACE
TRACE
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVE
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
LOW
1+
2+
3+
NEGATIVE
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
1+
2+
3+
NEGATIVE
1+
2+
3+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
04826807 Rev. A
Test
500 Clinitek 200+
POSITIVE
NEGATIVE
POSITIVE
TRACE
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
3.4-33.9 mg/mmol ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
NORMAL DILUTE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
French Conventional with PLUS System set to OFF
Supports Clinitek 200+ Program G4
Test
500 Clinitek 200+
TRACES
2.5 g/L
5.0 g/L
≥10.0 g/L
NEGATIF
1.0 g/L
2.5 g/L
5.0 g/L
≥10.0 g/L
FAIBLE
MOYEN
FORT
NEGATIF
FAIBLE
MOYEN
FORT
TRACES
0.15 g/L
0.4 g/L
≥0.8 g/L
NEGATIF
TRACE
0.15 g/L
0.4 g/L
≥0.8 g/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-LYSE
TRACES-INTACT
env. 25 GR/uL
env. 80 GR/uL
env. 200 GR/uL
NEGATIF
env. 10 GR/uL
env. 10 GR/uL
env. 25 GR/uL
env. 80 GR/uL
env. 200 GR/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIF
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVE
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIF
0.3 g/L
1.0 g/L
3.0 g/L
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
POSITIF
NEGATIF
POSITIF
env. 15 GB/uL
env. 70 GB/uL
env. 125 GB/uL
env. 500 GB/uL
NEGATIF
env. 15 GB/uL
env. 70 GB/uL
env. 125 GB/uL
env. 500 GB/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
30-300 mg/g ANORMAL
>300 mg/g ANORMAL
ELEVE
<30 mg/g NORMAL
30-300 mg/g ANORMAL
>300 mg/g ANORMAL
ELEVE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL, DILUEE
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL, DILUEE
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
Invalid Result Value ERREUR ERREUR
Color (COL) JAUNE CLR.
JAUNE
JAUNE FONC.
ORANGE CLR.
ORANGE
ORANGE FONC.
ROUGE CLR.
ROUGE
ROUGE FONC.
VERT CLR.
VERT
VERT FONC.
BLEU CLR.
BLEU
BLEU FONC.
MARRON CLR.
MARRON
MARRON FONC.
PAILLE
JAUNE
JAUN FONCE
AMBRE
ORANGE
ORANGE
ROUGE
ROUGE
ROUGE
VERT
VERT
VERT
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
Clarity (ASP) LIMPIDE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
LIMPIDE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
04826807 Rev. A
French Conventional with PLUS System set to ON
Supports Clinitek 200+ Program G40100
Test
500 Clinitek 200+
TRACES
1+
2+
3+
NEGATIF
TRACES
1+
2+
3+
1+
2+
3+
NEGATIF
1+
2+
3+
TRACES
1+
2+
3+
NEGATIF
TRACES
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-LYSE
TRACES-INTACT
1+
2+
3+
NEGATIF
TRACES
TRACES
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIF
TRACES
1+
2+
3+
NEGATIF
TRACES
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIF
FAIBLE
1+
2+
3+
NEGATIF
FAIBLE
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIF
1+
2+
3+
NEGATIF
1+
2+
3+
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
POSITIF
NEGATIF
POSITIF
TRACES
1+
2+
3+
NEGATIF
TRACES
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g ABNORMAL
ELEVE
<30 mg/g, NORMAL
30-300 mg/g, ANORMAL
>300 mg/g, HIGH
ANORMAL ELEVE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL, DILUEE
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL, DILUEE
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL
300 mg/g, ANORMAL
>500 mg/g, ANORMAL
Color (COL) JAUNE CLR.
JAUNE
JAUNE FONC.
ORANGE CLR.
ORANGE
ORANGE FONC.
ROUGE CLR.
ROUGE
ROUGE FONC.
VERT CLR.
VERT
VERT FONC.
BLEU CLR.
BLEU
BLEU FONC.
MARRON CLR.
MARRON
MARRON FONC.
PAILLE
JAUNE
JAUN FONCE
AMBRE
ORANGE
ORANGE
ROUGE
ROUGE
ROUGE
VERT
VERT
VERT
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
LIMPIDE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
04826807 Rev. A
French S.I. with PLUS System set to OFF
Supports Clinitek 200+ Program H4
Test
500 Clinitek 200+
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIF
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
FAIBLE
MOYEN
FORT
NEGATIF
FAIBLE
MOYEN
FORT
TRACES
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIF
TRACES
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-INTACT
TRACES-LYSE
FAIBLE
MOYEN
FORT
NEGATIF
TRACE
TRACE
FAIBLE
MOYEN
FORT
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIF
TRACES
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIF
TRACE
0.3 g/L
1.0 g/L
≥3.0 g/L
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIF
TRACES
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIF
TRACE
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
Protein (PRO)
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIF
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIF
0.3 g/L
1.0 g/L
3.0 g/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
04826807 Rev. A
Test
500 Clinitek 200+
POSITIF
NEGATIF
POSITIF
TRACES
FAIBLE
MOYEN
FORT
NEGATIF
TRACE
FAIBLE
MOYEN
FORT
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
3.4-33.9 mg/mmol
ANORMAL
> 33.9 mg/mmol ANORMAL
ELEVE
3.4-33.9 mg/mmol
ANORMAL
ELEVE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL, DILUEE
NORMAL
17.0 mg/mmol ANORMAL
>56.6 mg/mmol ANORMAL
NORMAL, DILUEE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
Color (COL) CLR. JAUNE
JAUNE
FONC. JAUNE
CLR. ORANGE
ORANGE
FONC. ORANGE
CLR. ROUGE
ROUGE
FONC. ROUGE
CLR. VERT
VERT
FONC. VERT
CLR. BLEU
BLEU
FONC. BLEU
CLR. MARRON
MARRON
FONC. MARRON
PAILLE
JAUNE
JAUN FONCE
AMBRE
ORANGE
ORANGE
ROUGE
ROUGE
ROUGE
VERT
VERT
VERT
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
LIMPIDE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
04826807 Rev. A
French S.I. with PLUS System set to ON
Supports Clinitek 200+ Program H4
Test
500 Clinitek 200+
TRACES
1+
2+
3+
NEGATIF
TRACE
1+
2+
3+
1+
2+
3+
NEGATIF
1+
2+
3+
TRACES
1+
2+
3+
NEGATIF
TRACE
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (SNG) NEGATIF
TRACES-LYSE
TRACES-INTACT
1+
2+
3+
NEGATIF
TRACES
TRACES
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIF
TRACES
1+
2+
3+
NEGATIF
TRACE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVE
FAIBLE
1+
2+
3+
NEGATIF
FAIBLE
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIF
1+
2+
3+
NEGATIF
1+
2+
3+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
3.2 umol/L
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
04826807 Rev. A
Test
500 Clinitek 200+
POSITIF
NEGATIF
POSITIF
TRACES
1+
2+
3+
NEGATIF
TRACE
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
0.9 mmol/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
3.4-33.9 mg/mmol ANORMAL
ELEVE
3.4-33.9 mg/mmol ANORMAL
ELEVE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL, DILUEE
NORMAL
NORMAL, DILUEE
NORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
Color (COL) CLR. JAUNE
JAUNE
FONC. JAUNE
CLR. ORANGE
ORANGE
FONC. ORANGE
CLR. ROUGE
ROUGE
FONC. ROUGE
CLR. VERT
VERT
FONC. VERT
CLR. BLEU
BLEU
FONC. BLEU
CLR. MARRON
MARRON
FONC. MARRON
PAILLE
JAUNE
JAUN FONCE
AMBRE
ORANGE
ORANGE
ROUGE
ROUGE
ROUGE
VERT
VERT
VERT
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
AUTRE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
LIMPIDE
LEG TROUB
TROUBLE
OPAQUE
AUTRE
04826807 Rev. A
German Conventional with PLUS System set to OFF
Supports Clinitek 200+ Program F4
Test
500 Clinitek 200+
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
SCHWACH
MAESSIG
STARK
NEGATIV
SCHWACH
MAESSIG
STARK
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
0 Ery/uL
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIV
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIV
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIV
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIV
30 mg/dL
100 mg/dL
300 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
POSITIV
NEGATIV
POSITIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
0 Leu/uL
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g STARK
ABNORMAL
<30 mg/g NORMAL
>300 mg/g STARK
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
P OK/ K GERING
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
P OK/ K GERING
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
Invalid Result Value FEHLER FEHLER
Color (COL) HELL GELB
GELB
DUNK. GELB
HELL ORANGE
ORANGE
DUNK. ORANGE
HELL ROT
ROT
DUNK. ROT
HELL GRUEN
GRUEN
DUNK. GRUEN
HELL BLAU
BLAU
DUNK. BLAU
HELL BRAUN
BRAUN
DUNK. BRAUN
HELL
GELB
DUNKEL
BRAEUNL.
ORANGE
ORANGE
ROT
ROT
ROT
GRUEN
GRUEN
GRUEN
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
Clarity (ASP) KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
04826807 Rev. A
German Conventional with PLUS System set to ON
Test
500 Clinitek 200+
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
1+
2+
3+
NEGATIV
1+
2+
3+
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OBL) NEGATIV
SPUR-LYSE
SPUR-ZELLEN
1+
2+
3+
NEGATIV
SPUR
SPUR
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIV
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIV
WENIG
1+
2+
3+
NEGATIV
WENIG
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIV
1+
2+
3+
NEGATIV
1+
2+
3+
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
POSITIV
NEGATIV
POSITIV
SPUR
1+
2+
3+
0 Leu/uL
SPUR
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g STARK
ABNORMAL
<30 mg/g NORMAL
>300 mg/g STARK
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
P OK/ K GERING
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
P OK/ K GERING
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
GELB
DUNK. GELB
HELL ORANGE
ORANGE
DUNK. ORANGE
HELL ROT
ROT
DUNK. ROT
HELL GRUEN
GRUEN
DUNK. GRUEN
HELL BLAU
BLAU
DUNK. BLAU
HELL BRAUN
BRAUN
DUNK. BRAUN
HELL
GELB
DUNKEL
BRAEUNL.
ORANGE
ORANGE
ROT
ROT
ROT
GRUEN
GRUEN
GRUEN
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
Clarity (ASP) KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
04826807 Rev. A
German S.I. with PLUS System set to OFF
Test
500 Clinitek 200+
5.5 mmol/L
14 mmol/L
28 mmol/L
≥55 mmol/L
NEGATIV
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
SCHWACH
MAESSIG
STARK
NEGATIV
SCHWACH
MAESSIG
STARK
SPUR
1.5 mmol/L
3.9 mmol/L
≥7.8 mmol/L
NEGATIV
SPUR
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
0 Ery/uL
Ca 10 Ery/uL
Ca 10 Ery/uL
Ca 25 Ery/uL
Ca 80 Ery/uL
Ca 200 Ery/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIV
SPUR
0.3 g/L
1.0 g/L
≥3.0 g/L
NEGATIV
SPUR
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIV
0.15 g/L
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIV
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIV
0.3 g/L
1.0 g/L
3.0 g/L
NEGATIV
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
POSITIV
NEGATIV
POSITIV
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
0 Leu/uL
Ca 15 Leu/uL
Ca 70 Leu/uL
Ca 125 Leu/uL
Ca 500 Leu/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol STARK
ABNORMAL
<30 mg/g NORMAL
>300 mg/g STARK
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
P OK/ K GERING
NORMAL
P OK/ K GERING
NORMAL
150 mg/mmol ABNORMAL
300 mg/mmol ABNORMAL
>500 mg/mmol ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
GELB
DUNK. GELB
HELL ORANGE
ORANGE
DUNK. ORANGE
HELL ROT
ROT
DUNK. ROT
HELL GRUEN
GRUEN
DUNK. GRUEN
HELL BLAU
BLAU
DUNK. BLAU
HELL BRAUN
BRAUN
DUNK. BRAUN
HELL
GELB
DUNKEL
BRAEUNL.
ORANGE
ORANGE
ROT
ROT
ROT
GRUEN
GRUEN
GRUEN
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
Clarity (CLA) KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
04826807 Rev. A
German S.I. with PLUS System set to ON
Test
500 Clinitek 200+
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
1+
2+
3+
NEGATIV
1+
2+
3+
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OBL) NEGATIV
SPUR-LYSE
SPUR-ZELLEN
1+
2+
3+
NEGATIV
SPUR
SPUR
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIV
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIV
WENIG
1+
2+
3+
NEGATIV
WENIG
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIV
1+
2+
3+
NEGATIV
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
16 umol/L
33 umol/L
66 umol/L
≥131 umol/L
0.2 mg/dL
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
POSITIV
NEGATIV
POSITIV
SPUR
1+
2+
3+
NEGATIV
SPUR
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
4.4 mmol/L
8.8 mmol/L
17.7 mmol/L
26.5 mmol/L
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
3.4-33.9 mg/mmol
ABNORMAL
> 33.9 mg/mmol STARK
ABNORMAL
<30 mg/g, NORMAL
30-300 mg/g, ABNORMAL
>300 mg/g, STARK
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
P OK/ K GERING
NORMAL
P OK/ K GERING
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
GELB
DUNK. GELB
HELL ORANGE
ORANGE
DUNK. ORANGE
HELL ROT
ROT
DUNK. ROT
HELL GRUEN
GRUEN
DUNK. GRUEN
HELL BRAUN
BRAUN
DUNK. BRAUN
HELL BLAU
BLAU
DUNK. BLAU
HELL
GELB
DUNKEL
BRAEUNL.
ORANGE
ORANGE
ROT
ROT
ROT
GRUEN
GRUEN
GRUEN
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
ANDERS
Clarity (ASP) KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
KLAR
FLOCKIG
S. FLOCKIG
TRUEB
ANDERS
04826807 Rev. A
Italian Conventional with PLUS System set to OFF
Supports Clinitek 200+ Program E4
Test
500 Clinitek 200+
1.0 g/L
2.5 g/L
5.0 g/L
≥10.0 g/L
NEGATIVO
0.1 g/dL
0.25 g/dL
0.50 g/dL
≥1.0 g/dL
LEGGERO
MEDIO
FORTE
NEGATIVO
LEGGERO
MEDIO
FORTE
TRACCE
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVO
TRACCE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACCE (LIS.)
TRACCE (INT.)
LEGGERO
MEDIO
FORTE
NEGATIVO
TRACCE
TRACCE
LEGGERO
MEDIO
FORTE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVO
TRACCE
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVO
TRACCE
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVO
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVO
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
Ca 15 Cel/uL
Ca 70 Cel/uL
Ca 125 Cel/uL
Ca 500 Cel/uL
NEGATIVO
Ca 15 Cells/uL
Ca 70 Cells/uL
Ca 125 Cells/uL
Ca 500 Cells/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
A:C Ratio (A:C) <30 mg/g NORMALE
30-300 mg/g
ABNORMALE
>300 mg/g MOLTO
ABNORMALE
<30 mg/g NORMALE
30-300 mg/g
ABNORMALE
>300 mg/g MOLTO
ABNORMALE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
URINA DILUITA
NORMALE
150 mg/g ABNORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
URINA DILUITA
NORMALE
150 mg/g ABNORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
NORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
Invalid Result Value ERRORE ERRORE
Color (COL) CHIA. GIALLO
GIALLO
SCUR. GIALLO
CHIA. ARANCIONE
ARANCIONE
SCUR. ARANCIONE
CHIA. ROSSO
ROSSO
SCUR. ROSSO
CHIA. VERDE
VERDE
SCUR. VERDE
CHIA. AZZURO
AZZURO
SCUR. AZZURO
CHIA. MARRONE
MARRONE
SCUR. MARONE
PAGLIER.
GIALLO
GIALLO SC.
AMBRA
ARANCIO
ARANCIO
ROSSO
ROSSO
ROSSO
VERDE
VERDE
VERDE
ALTRO
ALTRO
ALTRO
ALTRO
ALTRO
ALTRO
Clarity (ASP) LIMPIDA
LEG. TORB
TORBIDA
MOL.TORB
ALTRO
LIMPIDA
LEG. TORB
TORBIDA
MOL.TORB
ALTRO
04826807 Rev. A
Italian Conventional with PLUS System set to ON
Supports Clinitek 200+ Program E40100
Test
500 Clinitek 200+
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
1+
2+
3+
1+
2+
3+
NEGATIVO
1+
2+
3+
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
TRACCE (LIS.)
TRACCE (INT.)
1+
2+
3+
NEGATIVO
TRACCE
TRACCE
LEGGERO
MEDIO
FORTE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVO
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
BASSO
1+
2+
3+
NEGATIVO
BASSO
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
1+
2+
3+
NEGATIVO
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
TRACCE
1+
2+
3+
NEGATIVO
TRACCE
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
A:C Ratio (A:C) <30 mg/g NORMALE
30-300 mg/g
ABNORMALE
>300 mg/g MOLTO
ABNORMALE
<30 mg/g NORMALE
30-300 mg/g
ABNORMALE
>300 mg/g MOLTO
ABNORMALE
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
URINA DILUITA
NORMALE
150 mg/g ABNORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
URINA DILUITA
NORMALE
150 mg/g ABNORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMALE
300 mg/g ABNORMALE
>500 mg/g ABNORMALE
NORMALE
300 mg/g, ABNORMALE
>500 mg/g, ABNORMALE
Invalid Result Value ERRORE ERRORE
Color (COL) CHIA. GIALLO
GIALLO
SCUR. GIALLO
CHIA. ARANCIONE
ARANCIONE
SCUR. ARANCIONE
CHIA. ROSSO
ROSSO
SCUR. ROSSO
CHIA. VERDE
VERDE
SCUR. VERDE
CHIA. AZZURO
AZZURO
SCUR. AZZURO
CHIA. MARRONE
MARRONE
SCUR. MARONE
PAGLIER.
GIALLO
GIALLO SC.
AMBRA
ARANCIO
ARANCIO
ROSSO
ROSSO
ROSSO
VERDE
VERDE
VERDE
ALTRO
ALTRO
ALTRO
ALTRO
ALTRO
ALTRO
Clarity (ASP) LIMPIDA
LEG. TORB
TORBIDA
MOL.TORB
ALTRO
LIMPIDA
LEG. TORB
TORBIDA
MOL.TORB
ALTRO
04826807 Rev. A
Japanese Conventional with PLUS System set to OFF
Supports Clinitek 200+ Program B40101
Test
500 Clinitek 200+
Glucose (GLU) -
0.1 g/dL
0.25 g/dL
0.5 g/dL
≥1.0 g/dL
-
0.1 g/dL
0.25 g/dL
0.5 g/dL
≥1.0 g/dL
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-LYSED
+/-INTACT
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO®11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
-
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
-
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
-
30 mg/dL
100 mg/dL
300 mg/dL
-
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g, NORMAL
>300 mg/g, HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese Conventional with PLUS System set to ON
Test
Clinitek Advantus or 500 Clinitek 200+
Glucose (GLU) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-LYSED
+/-INTACT
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
-
+/-
1+
2+
3+
-
+/-
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
-
LOW
1+
2+
3+
-
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
-
1+
2+
3+
-
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g, NORMAL
>300 mg/g, HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese JCCLS with PLUS System set to OFF
Test
500 Clinitek 200+
Glucose (GLU) -
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
-
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-INTACT
+/-LYSED
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
-
+/-
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
-
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
-
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
-
30 mg/dL
100 mg/dL
300 mg/dL
-
30 mg/dL
100 mg/dL
300 mg/dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-
+
Leukocytes (WBC) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g, NORMAL
>300 mg/g, HIGH
ABNORMAL
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
04826807 Rev. A
Japanese JCCLS with PLUS System set to ON
Test
500 Clinitek 200+
Glucose (GLU) -
1+
2+
3+
4+
-
1+
2+
3+
4+
Bilirubin (BIL) -
1+
2+
3+
-
1+
2+
3+
Ketone (KET) -
+/-
1+
2+
3+
-
+/-
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (OB) -
+/-LYSED
+/-INTACT
1+
2+
3+
-
+/-
+/-
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
MULTISTIXÒ Group of
Test Strips
-
+/-
1+
2+
3+
-
+/-
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
-
LOW
1+
2+
3+
-
LOW
1+
2+
3+
MULTISTIX PRO‘ 6B
MULTISTIX PRO‘ 6K
-
1+
2+
3+
-
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
Urobilinogen (URO)
0.1 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
Nitrite (NIT) -+
-+
Leukocytes (WBC)
-
+/-
1+
2+
3+
-
+/-
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g, NORMAL
>300 mg/g, HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g, ABNORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g, ABNORMAL
>500 mg/g, ABNORMAL
YELLOW
DK. YELLOW
LT. ORANGE
ORANGE
DK. ORANGE
LT. RED
RED
DK. RED
LT. GREEN
GREEN
DK. GREEN
LT. BLUE
BLUE
DK. BLUE
LT. BROWN
BROWN
DK. BROWN
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) -
+/-
1+
2+
OTHER
-
+/-
1+
2+
3+
04826807 Rev. A
Portuguese Conventional with PLUS System set to OFF
Test
500 Clinitek 200+
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIVE
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
PEQUENO
MODERADO
GRANDE
NEGATIVE
SMALL
MODERATE
LARGE
INDICIO
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVE
TRACE
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (BLO) NEGATIVO
INDICIO-LISADO
INDICIO-INTACTO
PEQUENO
MODERADO
GRANDE
NEGATIVE
TRACE
TRACE
SMALL
MODERATE
LARGE
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strip
NEGATIVO
INDICIO
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVE
TRACE
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVE
15 mg/dL
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVE
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVE
POSITIVE
INDICIO
PEQUENO
MODERADO
GRANDE
NEGATIVE
TRACE
SMALL
MODERATE
LARGE
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
>300 mg/g HIGH
ABNORMAL
<30 mg/g NORMAL
>300 mg/g HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL DILUTE
NORMAL
150 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
Color (COL) CL. AMERELO
AMERELO
ES. AMERELO
CL. LARANJA
LARANJA
ES. LARANJA
CL. VERMELHO
VERMELHO
ES. VERMELHO
CL. VERDE
VERDE
ES. VERDE
CL. AZUL
AZUL
ES. AZUL
CL. MARROM
MARROM
ES. MARROM
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLARO
POUCO NEBULOSO
NEBULOSO
TURVO
OUTROS
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
Portuguese Conventional with PLUS System set to ON
Test
500 Clinitek 200+
INDICIO
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1+
2+
3+
NEGATIVE
1+
2+
3+
INDICIO
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
Blood (BLO) NEGATIVO
INDICIO-LISADO
INDICIO-INTACTO
1+
2+
3+
NEGATIVE
TRACE
TRACE
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVO
INDICIO
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
BAIXO
1+
2+
3+
NEGATIVE
LOW
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
1+
2+
3+
NEGATIVE
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
1.0 mg/dL
2.0 mg/dL
4.0 mg/dL
≥8.0 mg/dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVE
POSITIVE
INDICIO
1+
2+
3+
NEGATIVE
TRACE
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
30-300 mg/g ANORMAL
>300 mg/g ANORMAL
ALTO
<30 mg/g NORMAL
>300 mg/g HIGH
ABNORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
DILUIDO NORMAL
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL DILUTE
NORMAL
50 mg/g ABNORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL
300 mg/g ABNORMAL
>500 mg/g ABNORMAL
Color (COL) CL. AMERELO
AMERELO
ES. AMERELO
CL. LARANJA
LARANJA
ES. LARANJA
CL. VERMELHO
VERMELHO
ES. VERMELHO
CL. VERDE
VERDE
ES. VERDE
CL. AZUL
AZUL
ES. AZUL
CL. MARROM
MARROM
ES. MARROM
STRAW
YELLOW
DK YELLOW
AMBER
ORANGE
ORANGE
RED
RED
RED
GREEN
GREEN
GREEN
OTHER
OTHER
OTHER
OTHER
OTHER
OTHER
Clarity (CLA) CLARO
POUCO NEBULOSO
NEBULOSO
TURVO
OUTROS
CLEAR
SL CLOUDY
CLOUDY
TURBID
OTHER
04826807 Rev. A
Spanish with PLUS System set to OFF
Supports Clinitek 200+ Program D4
Test
500 Clinitek 200+
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
NEGATIVO
100 mg/dL
250 mg/dL
500 mg/dL
≥1000 mg/dL
BAJO
MODERADO
ALTO
NEGATIVO
BAJO
MODERADO
ALTO
INDICIOS
15 mg/dL
40 mg/dL
≥80 mg/dL
NEGATIVO
INDICIO
15 mg/dL
40 mg/dL
≥80 mg/dL
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
IND.HEMOLIZ.
IND.INTACTOS
Apr 25 Hem/uL
Apr 80 Hem/uL
Apr 200 Hem/uL
NEGATIVO
Apr 10 eri/uL
Apr 10 eri/uL
Apr 25 eri/uL
Apr 80 eri/uL
Apr 200 eri/uL
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strip
NEGATIVO
INDICIOS
30 mg/dL
100 mg/dL
≥300 mg/dL
NEGATIVO
INDICIO
30 mg/dL
100 mg/dL
≥300 mg/dL
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVO
15 mg/dL
30 mg/dL
100 mg/dL
300 mg/dL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
30 mg/dL
100 mg/dL
300 mg/dL
NEGATIVO
30 mg/dL
100 mg/dL
300 mg/dL
04826807 Rev. A
Test
500 Clinitek 200+
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
Apr 15 Leu/uL
Apr 70 Leu/uL
Apr 125 Leu/uL
Apr 500 Leu/uL
NEGATIVO
Apr 15 cel/uL
Apr 70 cel/uL
Apr 125 cel/uL
Apr 500 cel/uL
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
30-300 mg/g ANORMAL
>300 mg/g ALTAMENTE
ANORMAL
<30 mg/g, NORMAL
30-300 mg/g, ANORMAL
>300 mg/g, ALTAMENTE
ANORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
DILUIDO NORMAL
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
DILUIDO NORMAL
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
Color (COL) CL. AMARILLO
AMARILLO
OSC. AMARILLO
CL. NARANJA
NARANJA
OSC. NARANJA
CL. ROJO
ROJO
OSC. ROJO
CL. VERDE
VERDE
OSC. VERDE
CL. AZUL
AZUL
OSC. AZUL
CL. MARRON
MARRON
OSC. MARRON
COLURICA
AMARILLO
AM. OSCURO
AMBAR
ANARANJ
ANARANJ
ROJIZO
ROJIZO
ROJIZO
VERDOSO
VERDOSO
VERDOSO
OTROS
OTROS
OTROS
OTROS
OTROS
OTROS
Clarity (ASP) CLARO
LIG. TURB
TURBIA
MUY TURB
OTROS
CLARO
LIG. TURB
TURBIA
MUY TURB
OTROS
04826807 Rev. A
Spanish with PLUS System set to ON
Supports Clinitek 200+ Program D40100
Test
500 Clinitek 200+
INDICIOS
1+
2+
3+
NEGATIVO
INDICIO
1+
2+
3+
1+
2+
3+
NEGATIVO
1+
2+
3+
INDICIOS
1+
2+
3+
NEGATIVO
INDICIO
1+
2+
3+
1.010
1.015
1.020
1.025
≥1.030
≤ 1.005
1.010
1.015
1.020
1.025
≥1.030
IND.INTACTOS
IND.HEMOLIZ.
1+
2+
3+
NEGATIVO
INDICIO
INDICIO
1+
2+
3+
pH (pH) 5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
≥9.0
Protein (PRO)
Strips
NEGATIVO
INDICIOS
1+
2+
3+
NEGATIVO
INDICIO
1+
2+
3+
MULTISTIX PRO® 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
NEGATIVO
BAJO
1+
2+
3+
NEGATIVO
BAJO
1+
2+
3+
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NEGATIVO
1+
2+
3+
NEGATIVO
1+
2+
3+
04826807 Rev. A
Test
500 Clinitek 200+
Urobilinogen (URO) 0.2 U.E./dL
1.0 U.E./dL
2.0 U.E./dL
4.0 U.E./dL
≥8.0 U.E./dL
0.2 E.U./dL
1.0 E.U./dL
2.0 E.U./dL
4.0 E.U./dL
≥8.0 E.U./dL
POSITIVO
NEGATIVO
POSITIVO
INDICIOS
1+
2+
3+
NEGATIVO
INDICIO
1+
2+
3+
30 mg/L
80 mg/L
150 mg/L
10 mg/L
30 mg/L
80 mg/L
150 mg/L
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
10 mg/dL
50 mg/dL
100 mg/dL
200 mg/dL
300 mg/dL
30-300 mg/g ANORMAL
>300 mg/g ALTAMENTE
ANORMAL
<30 mg/g NORMAL
30-300 mg/g ANORMAL
>300 mg/g ALTAMENTE
ANORMAL
P:C Ratio (P:C)
MULTISTIX PRO 11
MULTISTIX PRO 10LS
MULTISTIX PRO 10LB
MULTISTIX PRO 10SB
MULTISTIX PRO 7G
DILUIDO NORMAL
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
DILUIDO NORMAL
NORMAL
150 mg/g ANORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
MULTISTIX PRO 6B
MULTISTIX PRO 6K
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
NORMAL
300 mg/g ANORMAL
>500 mg/g ANORMAL
Color (COL) CL. AMARILLO
AMARILLO
OSC. AMARILLO
CL. NARANJA
NARANJA
OSC. NARANJA
CL. ROJO
ROJO
OSC. ROJO
CL. VERDE
VERDE
OSC. VERDE
CL. AZUL
AZUL
OSC. AZUL
CL. MARRON
MARRON
OSC. MARRON
COLURICA
AMARILLO
AM. OSCURO
AMBAR
ANARANJ
ANARANJ
ROJIZO
ROJIZO
ROJIZO
VERDOSO
VERDOSO
VERDOSO
OTROS
OTROS
OTROS
OTROS
OTROS
OTROS
Clarity (CLA) CLARO
LIG. TURB
TURBIA
MUY TURB
OTROS
CLARO
LIG. TURB
TURBIA
MUY TURB
OTROS
04826807 Rev. A
Appendix E: Glossary
A:C albumin to creatinine ratio
<ACK> Computer acknowledges that it received the data correctly,
analyzer to address the next data set.
ALB albumin
<BEL> single character request for identification message
BIL bilirubin
BLO blood
CAN Resets the analyzer data transfer functions to the default
values:
XON, output buffer clear, input buffer clear
Checksum Two hexidecimal digit checksum for verification of the data.
<CR> control code for the carriage return character
CRE creatinine
DC1 Enables data transmission from the Clinitek 50
XON is in effect.
DC2 Data prompt to transmit one data set.
The Ready screen must be displayed.
DC3 Stops data transmission within one character. Analyzer
recognizes no input except DC1 (XON).
XOFF
<ENQ> Send instrument ID message.
XOFF is in effect.
<ETX> control code for the end of text character
GLU glucose
KET ketone
LEU leukocyte
<LF> control code for the line feed character
Marking Transmit signal is at negative levels.
Mpbs Megabytes bits per second
<NAK> Computer did not receive the data correctly, analyzer not to
address the next data set.
NIT nitrate
pH pH
P:C protein to creatinine ratio
PRO protein
2 CLINITEK Advantus and CLINITEK 500 Interface Specification: Glossary
04826807 Rev. A
SG Specific Gravity
Spacing Transmit signal is at positive levels.
<STX> control code for the tart of text character
URO Urobilinogen

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Clinitek AdvantusTM and Clinitek® 500 Analyzers

Using this Manual

Conventions Used in this Manual

Analyzer Flow Computer or LIS

Table continues on the next page.

3 Formatting Test Records

Appendix A: Safety Instructions

Appendix B: Service, Ordering, and

Information for Technical Assistance

Appendix C: Result Unit Tables

Appendix D: Clinitek 200/200+ Emulation

Result Value Conversions from Clinitek Advantus and

Result Value Conversions from Clinitek Advantus and

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