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Air jet sieve e200LS Security

Air jet sieve e200LS Security
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An air jet sieve is an optimal solution for particle size analysis of fine powders, including cohesive products with bad flow properties.

The principle of an air jet sieve guarantees exact and reproducible results which made it possible to include the HOSOKAWA ALPINE e200LS air jet sieve into the State Pharmacopoeia of Germany as a standard method of particle size analysis.

Automatic mesh size detection via a RFID chip eliminates human errors. The results of the analysis are stored in the archive and can always be printed as a table/curve, copied to a USB stick or into a folder in the company’s internal network.  

Model Features

Upgradeable at any time. eControl software options

LITE

  • Fast analysis
  • Simple one-touch operation
  • Graphic user interface
  • Underpressure (in Pa), sieving time, date and time are displayed
  • Underpressure manually adjustable
  • Connection of different vacuum cleaners (LITE only)
  • (comparable to A 200 LS)

BASIC

  • LITE Features, plus:
  • Fast, simple analysis of results (in table form)
  • Central parameter management of all sieves
  • Choice of 12 different languages
  • Balance communication via RS 232 interface
  • (comparable to 200 LS-N)

ULTIMATE

  • BASIC Features, plus:
  • Analysis of results against set-point specification (table and graph form)
  • Automatic backup
  • Automatic saving and printing
  • Individual display accuracy
  • Different diagram types
  • Parameter management per test sieve
  • Sieve set management (SOP)

SECURITY

  • ULTIMATE Features, plus:
  • Requirements for the software validation divided into ISPE GAMP 5, FDA 21 Part 11, EC GMP Annex 11 compliant
  • User administration
  • Password management
  • Audit trail – user activity monitoring and event logging
  • e-signature
  • Network connection required

The eControl version e200LS Security was created in order to meet the latest requirements of the pharmaceutical industry and includes the following advantages:

• requirements for the software validation divided into ISPE GAMP 5, FDA 21 Part 11, EC GMP Annex 11 compliant

• user administration

• password management

• audit trail – user activity monitoring and event logging

• e-signature