Please enter keywords to search.
Download Sell Sheet - English
Adaptable aseptic containment solution with user defined pressure and airflow regimes.
Premium handling of biopharmaceutical germ seed cells and aseptic cell processing. Premium solution for large volume sterility testing.
Uni-directional airflow – 0.45m/s ± 20% measured 150mm from the distribution screen face during normal operation provides ISO 5 / Grade A aseptic environment.
Knife edge gel sealed U15 supply and optional U15 return filters.
Gasket sealed F8 room inlet and outlet filters.
System automatically compensates for containment breach in +ve or -ve mode via an egress or inward rush respectively.
Optional VHP Ports for automated aseptic processing allowing chamber or system decontamination.
Optional humidity/temperature sensors for environmental monitoring.
Biodecon loop for decontamination of viable or non viable monitoring systems.
External sensors protected by instrument filters.
Optional distribution manifold allows more accurate sampling of upstream filter PAO concentration (since this manifold draws in PAO it is advice that this be cleaned before every filter change).
Filter scanning ports for downstream filter integrity testing.
Automated raise/lower carriage system via user ID input allows isolator to be raised to operator defined ergonomic height.
Safe change gloveport assembly allows for either single piece or split cuff gloves to be change without any breach in isolator condition.
Enhanced uniformity and entrainment of powders via our PLF screens.
Smooth flushed interior of isolator glazing means less crevices to improve clean ability / decontamination.
Glazing is made of toughened laminated safety glass.
PLF diffuser screens provides uniform airflow throughout the interior workzone.
Single piece chamber fabricated of ss316L hand polished to less than 0.4Microns with 19mm coved corners.
Stainless steel is passivated post-fabrication with citric acid.
Clean sanitary finishing and perforated multi-piece worktray enhances uni-directional airflow for ultimate entrainment of contaminants and of potent powders.
International brand safe change filters means lower replacement costs and quicker turnaround time.
HMI/PLC control architecture with 4 defined levels of hierarchy.
Access for common replaceable items such as lights and ballasts are done all from the front of the unit.
Integrated automated pressure testing.
Filters can be upgraded to safe change with additional bags and BIBO rings.
Bypass option can be retrofitted with additional safe change housing.
System runs in any of the following airflow regimes in both positive and negative and can be configured in-situ by administrator access.
Volt free contacts provided for client connection to HVAC and optional 21 CFR Part 11 chart recorder for storing of process data.
Carboys for draining of fluid waste.
Additional factory integrated transfer ports.
Custom sanitary shelving or IV bars.
Sterility test pumps.
Esco Pharma has been awarded to be the ...
“The 9th International Exhibition on COMPLETE Pharma Manufacturing”
Venue: International ...
Venue: Javits Center, 655 W 34th St. New York, ...
Venue: Swissôtel Congress Centrum Düsseldorf / Neuss Rheinallee ...
Venue: Cairo International Convention Center, Cairo, Egypt ...
“25th ProPak Asia - International Processing, Filling & ...
Venue: Las Vegas Convention Center, Las Vegas, Nevada ...
“Trade Fair for Processing, Analysis, and handling of ...
Venue: Orange County Convention Center 9400 Universal Boulevard, ...
Esco Pharma Pte Ltd
21 Changi South Street 1 Singapore 486777
Tel: +65 65420833
Fax: +65 65426920
Esco Technologies, Inc.
2512 Metroprolitan Dr, Suite 120-B
Feasterville-Trevose, PA 19053-6738
Tel: 1 215-322-2155
Esco Gb Ltd
Unit 9, Century Park Networkcentre,
Dearne Lane, Manvers, Rotherham,
South Yorkshire, S63 5DE.
Tel: +44 (0) 1709 761 669