Esco Technologies - DFB-1.5S1-C
Manufactured by Esco Technologies
Pharmacon™ Downflow Booths
Downflow Booths provide containment by utilizing high velocity air to capture airborne dust particles. Downflow Booths are versatile devices that can:
• Be used to control exposure risk to hazardous materials for a wide variety of equipment and processes.
• When used correctly, provide Operator Exposure Levels (OEL's) =100 micrograms/meter3 over an 8 hour Time Weighted Average (TWA).
• Enhance cGMP practices.
• Be used to control exposure risk to hazardous materials for a wide variety of equipment and processes.
• When used correctly, provide Operator Exposure Levels (OEL's) =100 micrograms/meter3 over an 8 hour Time Weighted Average (TWA).
• Enhance cGMP practices.
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Features of DFB-1.5S1-C
- Modular, easy-to-clean rigid design with minimal joints. * Single, Two Stage or Three Stage HEPA/ULPA filtration can be accommodated. * Removable bulkhead panels enable access to fine dust filter for service from inside the booth. * Re-circulatory Airflow or Single Pass Airflow if solvent or hazardous fumes are present in the process (may also require ex-plosion proof electrics). * Cooling Coils can be fitted to offset heat gains in re-circulatory airflow systems. * HEPA/ULPA gel-seal downflow filters are replaceable from within the booth, gel-seal is more reliable than conventional gasketed seals. * Voltage-compensating blower(s) ensure stable airflow. * Magnehelic gauges provide convenient and reliable means for monitoring booth airflow. * Booths ship knocked-down for site assembly. * Compact ceiling and rear plenums maximize usable work area while minimizing floor space. * IQ/OQ protocols available. * Energy-efficient tear-drop light fittings minimize airflow disruption. * Comprehensive factory and site acceptance tests include: filter integrity, particle count (air cleanliness), downflowvelocity and uniformity, exhaust velocity/volume, containment zone verification, noise level, light intensity, temperature rise and electrical safety. * Containment performance verified according to the ISPE Good Practice Guide,Assessing the Particulate Containment Performance of Pharmaceutical Equipment.
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