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Air disinfection units

Air disinfection units are utilized in cleanrooms to maintain the required level of microbiological purity. They are essential for pharmaceutical and biotechnological manufacturing, medical institutions, laboratories, and other facilities with stringent sanitary safety requirements. These systems actively eliminate airborne pathogens, ensuring the environment remains compliant with sterile processing standards.

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Design and Key Features

The construction of air disinfection units is engineered to meet the rigors of sterile environments:

  • Durable Materials: The housing is made of materials resistant to aggressive disinfectants and repeated cleaning cycles, including high-grade AISI 304 stainless steel.

  • Advanced Filtration: Units can be equipped with high-efficiency filters (HEPA or ULPA) and/or integrated UV modules for supplementary germicidal irradiation.

  • Flexible Installation: Support for various mounting configurations, including wall-mounted, floor-standing, or fully integrated into existing HVAC (ventilation) systems.

  • Operational Efficiency: Designed for low noise levels and ease of maintenance, allowing for filter replacement and UV lamp servicing without compromising room integrity.

  • Scalable Performance: Various capacities are available to match the specific volume of the room and the targeted cleanliness class (ISO/GMP).

Validation and Compliance

To ensure the reliability of controlled environments, air disinfection units undergo rigorous testing and documentation:

  • GMP Annex 11: Systems are validated in accordance with Annex 11 of the Good Manufacturing Practice (GMP) guidelines, ensuring that automated systems function reliably and maintain data integrity.

  • GAMP 5 (Good Automated Manufacturing Practice): Compliance with GAMP 5 recommendations, developed by the International Society for Pharmaceutical Engineering (ISPE), guarantees a risk-based approach to the design and operation of automated manufacturing equipment.

These units are a critical component in the multi-stage defense against cross-contamination, protecting both the integrity of the product and the safety of the personnel.