Perfected for the use of the hot water cascading method, the Fluipharm® offers everything necessary for research and development, the production of sterile materials and, last but not least, the treatment of parenteral solutions in hospital pharmacies. After all, fast sterile reprocessing is a key ingredient to the success of any business in the pharmaceutical or biotech industry.
Sterilization of liquids in closed containers.
MMM developed the Fluipharm® in response to the stringent requirements of the pharmaceutical industry on design and process reliability. The machine uses the water cascading method and is ideally suited for sterilizing solid and porous materials as well as liquids in tightly sealed containers.
The Fluipharm® complies with the Pressure Equipment Directive (PED) 2014/68/EU and the Machinery Directive 2006/42/EC, CE marking according to PED 2014/68/EU. The standards applied are: DIN 58950-2 Sterilization, AD 2000 Design of Pressure Vessels and DIN EN 62304 Medical device software.
Siemens controller
12” or 15” display, or customer-specific size
Clamp or aseptic threaded connections
FDA-compliant sealing materials and lubricants (21 CFR)
F0 value controlled process sequence
Sterile filtration of compressed air
Air-tight separation
“Vacuum programs” equipment package
Additional programs: “Vacuum drying, ampule check, rinse cycle”
Heat exchanger with heating steam
Connection to cooling circuit
Heat exchanger fully drainable on product side, hygienic process connections
Barcode reader for identifying the material being loaded
Remote diagnostics, central control room