EC FFU | Energy Star Certified Smart Air System | Pharma-Grade Real-Time Monitoring & Ultra-Low Noise

The EC FFU 1175X575X215 revolutionizes cleanroom efficiency with its industry-first Energy Star 4.0 certification, specifically engineered for sterile compounding pharmacies, gene therapy labs, and ISO Class 5-8 modular facilities. Combining a 1175×575×215mm ultra-slim chassis with edge computing capabilities, this FFU delivers 850m³/h airflow while maintaining <0.1% velocity deviation across critical zones.

Key Features

1. Robust Construction: Galvanized aluminum plate ensures durability and corrosion resistance.

2. Energy-Efficient Motor: Nidec DC motor with metal impeller delivers precise airflow control and ultra-low power consumption.

3. Adjustable Airflow: Wind speed adjustable between 0.45–0.75 m/s (±5%) for flexible cleanroom requirements.

4. H13 Filtration: Non-partitioned HEPA filter achieves 99.995% efficiency at 0.3μm particles with low initial resistance (≤125Pa).

5. Ultra-Low Power: Rated power of 36W–102W (±5W) ensures energy-efficient operation.

6. Quiet Performance: Engineered for 48–58 dB (±5 dB) noise levels at 1.5m below the filter.

7. Stable Operation: Vibration limited to <5μm for precision-sensitive environments.

Application Scenarios

Cleanroom air purification in pharmaceutical, electronics, and biotechnology facilities.
Manufacturing zones requiring ISO-certified H13 filtration with adjustable airflow.
Energy-sensitive facilities demanding ultra-low power consumption and quiet operation.

FAQ :
1. How does the Energy Star certification reduce operational costs for 24/7 cleanroom facilities?
The EC motor technology cuts energy consumption by 30–40% compared to traditional AC FFUs, achieving <0.8 kW/m³/h efficiency. Energy Star compliance ensures long-term savings while meeting ISO 14644-1 airflow stability requirements.
2. Can the real-time monitoring system integrate with pharmaceutical batch records for FDA audits?
Yes, the pharma-grade IoT sensors track HEPA filter ΔP, airflow velocity, and particle counts, with 21 CFR Part 11-compliant data logs for seamless audit trails. Alerts trigger via SMS/email at 80% resistance thresholds to prevent unplanned downtime.
3. How does ultra-low noise (<45 dB) benefit sensitive environments like cell therapy labs?
The aerodynamic impeller and vibration-damped housing maintain noise levels below WHO lab guidelines, eliminating disruptions to sterility workflows or precision instruments (e.g., PCR equipment).