Autoclave for the pharmaceutical industry Fluipharm®
for researchhospitalhot water

Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water
Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water
Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water - image - 2
Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water - image - 3
Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water - image - 4
Autoclave for the pharmaceutical industry - Fluipharm® - MMM Group - for research / hospital / hot water - image - 5
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Characteristics

Applications
hospital, for the pharmaceutical industry, for research
Sterilization procedure
hot water
Configuration
horizontal
Function
automatic
Capacity

644 l, 871 l, 1,267 l
(170.13 gal, 230.09 gal, 334.71 gal)

Width

1,900 mm
(75 in)

Height

1,918 mm
(75.5 in)

Depth

1,360 mm, 1,710 mm, 2,310 mm
(54 in, 67 in, 91 in)

Description

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

Exhibitions

Meet this supplier at the following exhibition(s):

ArabHealth 2025
ArabHealth 2025

27-30 Jan 2025 Dubai (United Arab Emirates) Stand H3.C31

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    *Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.