Lasair III0 pages

Lasair III®

Without measurement there is no control.

Aerosol Particle Counter Models 310B, 310C, 350L, 5100

BENEFITS
•t ISO 21501-4 compliant with a built-in
Pulse Height Analyzer (PHA)

•t 100 LPM, 50 LPM, or 1 CFM flow rates

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The Lasair III Particle Counter sets the standard for portable aerosol
particle counters and meets the requirements of ISO 21501-4.
The Lasair III Particle Counter is available in three different flow rate
configurations (1 CFM, 50 LPM and 100 LPM) to meet a variety of
cleanroom applications. It can be used for routine remote and mobile
cleanroom monitoring. Interactive software steps the user through the
ISO 14644-1, EC GMP Annex 1, China GMP, and FS 209E room certification
process.
Cleanroom certification results are available through a local printout,
downloadable via USB in a secure format, or through the use of external
software packages such as DataAnalyst, Facility Net or Pharmaceutical Net
software.
The large easy-to-read IR touchscreen works with gloves – no stylus
needed.
The rugged chemical-resistant enclosure is lightweight for portability and
has a streamlined design to minimize particle traps, making the unit easy
to clean. Power is provided to the unit through the use of the on-board
hot-swappable batteries. Power can also be provided through the use of
an external AC power source, which can simultaneously power the unit
and charge the on-board batteries.
The Lasair III Particle Counter accepts inputs from a wide range of
environmental sensors through the four built-in 4-20 mA inputs. Wireless
network communications are made easy with an externally-mounted
wireless adapter, simplifying communications with network systems.
The unit can be remotely managed via the built-in web browser function
or through Ethernet to Pharmaceutical Net , Facility Net, or FacilityPro®
software.

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– 100 LPM flow samples 1 m3 in 10
minutes
Large IR touchscreen for simplified use
Quiet pump improves work environment
Calculates and creates reports for ISO
14644-1, EC GMP Annex 1, China GMP, and
FS 209E
21 CFR Part 11 compliant download
Comprehensive validation manual makes
it easy to meet pharmaceutical regulatory
requirements
Operates in cleanrooms via a web
browser: Set up, sample, display, print,
download data
Choose from 11 languages for display and
printout
Removable batteries with optional
external charger for continuous mobile
use
Stores sampling recipes to reduce
operator errors
Long-term data archiving with
DataAnalyst software
Local printout for immediate hardcopy
results
USB electronic printouts for long term
storage
CSV file download for easy data
integration
Web browser for simplified remote
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APPLICATIONS
•t Cleanroom monitoring
•t Facility certification for ISO, EC GMP, China
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GMP, FS 209E
Trend analysis
Statistical process control
Troubleshooting particle excursions
Manifold compatible
Portable or dedicated use