The Cytiva™ drug product filtration system operates using configurable recipe-controlled phases to automatically perform terminal sterilization prior to filling with maximum product recovery using standard flow kits. It has been designed to support EU GMP Annex 1: Manufacture of sterile medicinal products requirements for contamination control strategies with automated in situ pre-use post-sterilisation integrity testing (PUPSIT) and post-use integrity testing of sterile filters.
Fully automated sterile filtration with configurable recipe-controlled phases
Automated PUPSIT and post- use integrity testing
Enhanced product recovery method for reduced product loss
Compatible with a wide range of filter sizes
Single-use flow kits for rapid turnaround between batches
One system for both single and redundant filtration
Integrated human machine interface (HMI)
Product specifications
Dimensions (W × D × H)
118 × 105 × 72 cm
IP (Ingress Protection) Rating
IP54
Materials of construction
Stainless steel 1.4301 (304)
Surface Finish
Cold rolled steel with minimal work marks (typically Ra < 1.2 µm)
Weight (kg)
135