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2026-07-08

II. Key Benefits of High Efficiency Top Seal Filters for Pharmaceutical Applications
Top fluid chamber seal design – easy installation and replacement where ceiling space is limited
The top of the equipment is equipped with a one-piece blue chamber for liquid sealing. When installed in place, liquid silicone is poured into the chamber, forming a seamless sealed layer that completely eliminates gaps for air leaks around the perimeter of the frame. Unlike traditional side fluid chamber filters, the top seal design is suitable for small service ceiling spaces. To replace the filter element, simply open the top service hatch without dismantling the suspended ceiling frame. This significantly reduces the time it takes to stop production to modernize a clean shop and reduces losses from interrupting the production of medicines.
Ultra-fine glass fiber filter material with low dust emission - prevents re-contamination of medications
Inside, a dense filter material made of ultra-fine glass fiber is used, which stably provides the required efficiency of retaining suspended particles of 0.3 microns in size, effectively retaining bacteria, spores, and dust aerosols in the air. Before leaving the plant, the filter material is cleaned from dust in a dust-free room, during operation it does not emit fibers and volatile organic compounds (VOCs), eliminates cross-contamination of raw materials and finished dosage forms, and complies with sterile pharmaceutical control standards.
Lightweight aluminum alloy frame, corrosion resistant - suitable for workshops with constant temperature and humidity
The one-piece aluminum alloy frame with anti-oxidation surface treatment does not rust or deform during long-term operation in workshops with temperatures of 18–26 °C and relative humidity of 45–65%. The frame is equipped with locking locks, allowing one technician to hang and position the filter, reducing labor costs for on-site installation.
Comprehensive PAO Leak Testing – Fully Compliant with Factory Testing Regulations
Each filter is leak tested with a PAO aerosol in a Class 10,000 dust-free environment, leak data for each product is recorded, and complete test reports are included with the filters. This simplifies inspections according to the GMP standard and archiving of documentation by pharmaceutical enterprises, eliminating risks during inspections by regulatory authorities.

The HEPA filter with gel seal has undergone a sealing process and is shipped directly to the pharmaceutical company's facility where they are renovating their sterile facility.