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BIOLABO Diagnostics KENZA 240 TX User Manual

BIOLABO Diagnostics KENZA 240 TX
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Compliance
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Certification
ISO 9001:2008
ISO 13485:2004
KENZA 240 TX
Automatic Biochemistry Analyser
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User’s Guide
KENZA 240TX / ISE_EN.DOC V 2011/02
Device of In Vitro Diagnosis for analyses of Medical Biology (Clinical Chemistry)
Only for professional use - Respect the legislation in force
Conform to the Directive 98/79/CE
Code GMDN: 15165
BIOLABO SA (paid-up capital 119 700 €)
Les Hautes Rives
F-02160 MAIZY (FRANCE)
Tel: (33) 03 23 25 15 50
Fax: (33) 03 23 256 256
Headquarter: 02220 PAARS (FRANCE)
Email: info@biolabo.fr
WEB: http://www.biolabo.fr

Table of Contents

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BIOLABO Diagnostics KENZA 240 TX Specifications

General IconGeneral
BrandBIOLABO Diagnostics
ModelKENZA 240 TX
CategoryMeasuring Instruments
LanguageEnglish

Summary

General Information

Technical Specifications

Detailed specifications of the analyser's operation, performance, and components.

Installation

Unpacking the Kenza 240 TX / ISE

Instructions for inspecting and unpacking the instrument and accessories.

Installation of the Instrument

Procedure for safely placing and setting up the analyser.

Installation of the Software

Steps to install the analyser's management software on a computer.

Starting Operations

Initial procedures for priming the system and performing basic checks.

Preliminary Operations

Switching on the Instrument

Step-by-step guide to power on the external computer and the analyser.

Methods Programming

Method Menu

Accessing functions for managing, programming, and calibrating methods.

Program a New Method

Detailed steps for defining new analytical methods and parameters.

Modify a Method

Procedure for editing existing method parameters.

Calibrations and Controls

Calibrations and Control Menu

Accessing calibration and control functions and options.

Carry out Calibrations and Controls

Procedure for performing calibrations and running quality controls.

QC Values and Charts

Monitoring quality control data, statistics, and Westgard rules.

Prepare the Run

Registering Patients

Steps for entering patient data and selecting tests.

Prepare Samples

Guidelines for preparing serum cups and primary tubes for analysis.

Prepare Reagents

Checking reagent positions and identifying missing or insufficient reagents.

Start Routine

Procedures for initiating the analytical run, including checks and selections.

Select the Parameters to be Used

Choosing specific tests for the current run or future runs.

Manage Reagents

Checking reagent availability and volumes for selected tests.

Start the Run

Initiating calibrations, controls, and patient sample analyses.

During the Run...

Instrument Manipulation

Ensuring the instrument cover is closed for safe operation.

STAT Sample – Urgent Analysis

Prioritizing and running urgent samples immediately.

After the Run

Check Results

Accessing and reviewing patient results after the analysis is complete.

Repeat Analyses After the Run

Requesting re-analysis of tests after the run has finished.

Print Results

Generating reports and printing patient results.

MAINTENANCE

Daily Maintenance

Routine tasks for maintaining the analyser daily.

Preventive Maintenance Schedule and Report

Guidelines for scheduled preventive maintenance and record keeping.