FAF Products
Top Gel Seal Mini-pleat HEPA filter
Product Overview
• Minimum 99.99% at 0.3μm, H13, and 99.995% at MPPS, H14.
• Polyalphaolefin (PAO) compatible.
• Lowest pressure drop mini-pleat HEPA filter available for pharma, life sciences.
• Lightweight galvanized or aluminum or stainless steel’s frame available.
• Gel, gasket, or knife-edge seal available.
• Thermoplastic hot-melt separators.
Typical Applications
• Pharmaceutical
• Life Sciences
• Biosafety
• Healthcare
• Pill Encapsulation
FAF’S HEPA Filters
Designed specifically for the unique requirements and challenges of the pharmaceutical industry, the mini-pleat HEPA filter has the proven durability, polyalphaolefin (PAO) compatibility, high particulate filtration efficiency, and lowest pressure drop to meet the demands of pharmaceutical manufacturing. It is the best choice for the most demanding applications, saving both time and money, while reducing contamination risk and invasive unscheduled downtime. With the lowest Total Cost of Ownership of all mini-pleat HEPA filters, it will help protect your environment, reduce your business risk, and optimize your clean air related spending.
Proven Reliability with Exceptional Performance
Designed to increase cleanroom uptime and reduce the risks associated with pharmaceutical manufacturing.
Pharmaceutical grade microglass, delivering superior performance.
Extremely low off-gassing of chemical components, resulting in the highest quality clean air available.
Lowest pressure drop mini-pleat HEPA filter available, reducing energy consumption for significant savings.
Manufactured, tested, and packaged in ISO 7 clean facilities to ensure the highest purity, quality, and consistency.
Reduce Operational Risk
The pharmaceutical industry estimates that 77% of production downtime can be attributed to failures of equipment and environmental problems. This downtime can be caused by HEPA filters failing. Effectively managing the risk and costs associated with successful operation requires utilizing HEPA filters with dramatically higher tensile strength that is highly resistant, thereby eliminating premature leaking and failure.
Increase Uptime
While FDA Testing Guidance requires critical room leak-testing certification twice a year, non-critical rooms require testing only once a year. ncreasing time between certifications results in less PAO exposure to the gel seal (gel degradation), lower labor costs, and increased production time.
The purpose of installed HEPA filter integrity testing, also called in-situ testing, is to confirm a flawless performance during normal operation. FAF’S filters can be scan tested with the industry standard photometer at the standard aerosol concentrations, as well as the low-aerosol concentration Discrete Particle Counter (DPC) method.
Negligible Off-Gassing
Extremely low off-gassing of chemical components, resulting in the highest quality clean air available.
