Import Air Cleaner — Buy in Bulk from Supplier in Turkey

The Air Cleaner from DFL Pharma & Medical is a high-efficiency air purification system designed for professional environments, including dental clinics. Models such as SafeAir and SafeAir Maxi feature a three-layer microbial gel filter (F5 UGMA Class) that captures viruses, bacteria, yeast and mould particles smaller than 0.10 microns with 99.9 percent efficiency. The systems integrate cold plasma generators to neutralise airborne pathogens and activated carbon filters to remove odours, gases and ozone.

SafeAir operates at 75 Watts with dimensions of 120x45x35 cm and weighs 28 kg, delivering 400,000 litres of filtered air per hour across areas up to 50 square metres. The SafeAir Maxi variant scales up to 145 Watts, 150x50x40 cm, 40 kg, and 1,000,000 litres per hour, covering spaces up to 350 square metres. Both models maintain noise levels below 22 dB, making them suitable for quiet clinical settings.

These units are targeted at healthcare providers, particularly dentists, who require high standards of air quality to protect staff and patients. The systems are designed for easy integration into existing HVAC setups or as standalone units. Buyers should confirm electrical compatibility, as the units are rated for 220 V power, and request filter replacement schedules to maintain optimal performance.

DFL Pharma & Medical is based in Ankara, Turkey, with a registered address at Eskisehir Yolu, Fatih Sultan Mahallesi, Dumlupınar Bulvarı, 2700. Cadde, No:3/1, Arpakule Cayyolu. The company holds a harbor trust tier on the platform, though its response rate and average response time are currently recorded as zero, indicating limited recent activity or engagement.

The supplier specialises in air purification systems for medical and dental applications, with products like the AirBlend GermBuster line. The listing highlights the technical capabilities of its units but does not provide details on certifications, production capacity or export experience. Buyers should verify compliance with medical device regulations in their target markets and request documentation such as CE marking or ISO 13485 certification.