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8.1 Changing the settings
The Settings menu is populated with various settings, some of which have default options which can
be changed to suit your individual preferences and geographical location. To change a setting, touch
to select a setting. A pop-up screen will appear. Select the required option from the pop-up screen
then touch the main screen behind or back key to exit.
Device settings
Language:
Device storage:
Camera gain:
Error reporting:
Notifications:
Select either ‘English’ or ‘French’.
Displays the total amount of internal memory used and the amount of
memory remaining.
Select either ‘Low’ (default) or ‘High’.
The ‘High’ setting will increase the brightness of the image compared to the
‘Low’ setting. The ‘Low’ setting should be suitable for most melting point
determinations.
Displays details of any errors in QR code format which can be sent to
Antylia Scientific Ltd
for diagnostic purposes.
Can be set such that the unit sends a notification for the following:
❖
Measurement completed.
❖
Calibration reminder – can be set to Never (default), Weekly,
Monthly, Bi-annually or Annually.
Date & time:
Check USB for
an update:
Protect settings:
About:
Display formats
Temperature units:
Time format:
Can be set for regional time zones. Set the date and local time before first
use.
Allows you to perform software updates from a USB flash drive. Updates
can be downloaded from www.
coleparmer
.com or contact
[email protected] See section 18 for how to perform a
software update.
Allows settings to be password-protected to stop any unauthorised changes.
Displays information about the currently installed version of software.
Select either ‘°Celsius’ or ‘°Fahrenheit’.
Select either ‘12 Hour’ or ‘24 Hour’.
Results
Save the melt video
Select ‘ON’ to save the melting video for future reference. Use the slider
with the report:
button to turn on or off.
Encrypt all results
Select ‘ON’ to encrypt the results files to prevent post-run editing. Use the
files:
slider button to turn on or off.
Note:
The
MP-800D
can serve as part of a US FDA 21 CFR part 11 compliant system relating to its
use to generated results in an electronic format. Results generated on the instrument can be copied
to a