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.
H model 969
1,000 x 650 x 990
1.918 x 1.900 x 1.360
H model 9612
1,000 x 650 x 1,340
1.918 x 1.900 x 1.710
H model 9618
1,000 x 650 x 1,940
1,918 x 1,900 x 2,310
Technical data subject to change without notice
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.
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