To Next PageTo Next PageWhat to do if unable to pipette suspension on target plate with BD Laboratory Equipment?
If you are unable to pipette suspension on a target plate, select 'Error Resolved', then select 'Start'.
What to do if there is an unexpected pipette tip attached to the pipettor of BD Laboratory Equipment?
If you encounter an unexpected pipette tip attached to the pipettor, remove the pipette tip from the pipettor.
What to do if unable to pick up a cuvette array in BD Kiestra IdentifA?
If you're unable to pick up a cuvette array, check the status in the cuvette drawer and restart.
What to do if the pipette tip straightness check failed in BD Laboratory Equipment?
If the pipette tip straightness check failed, replace the pipette tip rack with a new one.
General| Brand | BD |
|---|---|
| Model | Kiestra IdentifA |
| Category | Laboratory Equipment |
| Language | English |
Defines text formatting like bold and italics used in the manual for clarity.
Explains how safety messages (NOTE, CAUTION, WARNING) are presented and their meanings.
Lists and explains symbols used for safety, compliance, and device identification within the manual.
Clarifies that patient data shown is illustrative and not actual clinical information.
Describes the BD Kiestra™ IdentifA module's purpose for specimen preparation and organism identification.
Details the IdentifA module, user interface, and functional areas of the system.
Explains the IdentifA module's touchscreen interface for workflow actions and data entry.
Identifies the main areas of the IdentifA module for colony picking and suspension preparation.
Outlines crucial safety guidelines, operational limitations, and potential hazards of using the device.
Guides users on how to modify system settings for audible alerts, checks, and wait times.
Details how to configure the audible buzzer for system notifications and errors.
Specifies the time for the daily nephelometer check after module startup.
Specifies the time the system waits for cuvette arrays before proceeding with target spotting.
Defines the time the system waits before finishing target spotting if no new specimens arrive.
Details the steps for powering on the IdentifA module and initial system checks.
Explains how to log in to access basic and advanced functions of the IdentifA module.
Guides users on how to begin routine specimen processing after startup.
Describes how the system alerts users to events and the meaning of different notification indicators.
Explains how to temporarily halt module operations for maintenance or other tasks.
Covers tracking and replenishing essential reagents and consumables like pipette tips.
Instructions for loading new pipette tips into the module's drawers.
Provides instructions for replacing cuvette arrays, including indicator light meanings.
Guides users on how to replace reagent vials, including checking cap tightness.
Lists compatible MALDI targets and notes for their use.
Step-by-step guide for loading MALDI targets into the module, including barcode scanning.
How to safely stop the module's operation for maintenance or calibration.
Procedure for properly shutting down the IdentifA module after specimen processing is complete.
Procedures for handling and disposing of liquid and solid waste generated by the module.
Explains the importance and methods for cleaning and disinfecting the module components.
Lists recommended and compatible cleaning agents and disinfectants for the module.
Outlines different cleaning approaches: dry, wet, and combined cleaning techniques.
Details specific cleaning procedures for individual module components.
Procedures for cleaning up spills in specific areas of the module.
Guidelines for decontaminating the module after spills or contamination.
Outlines essential routine maintenance tasks for the module.
Describes the monthly and daily calibration procedures for the nephelometer.
Guides users on how to react to system alerts and errors promptly.
Lists common error codes, messages, and their corresponding resolution descriptions.
Evaluates the accuracy of the IdentifA module in picking designated colonies from culture plates.
Assesses the accuracy of organism identification using samples prepared by IdentifA.
Examines the consistency of organism identification results across modules, operators, and days.
Evaluates the module's ability to achieve expected identification at specified microbial suspension levels.
Assesses the potential for cross-contamination between samples within the IdentifA module.
Lists physical dimensions, weight, and environmental requirements for installing the module.
