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FSsmPharmaElements_EN.doc Sep-13
Thin film membrane (TFM*)
Average
permeate flow
gpd (m3/day)
Maximum Operating Pressure
Continuous operation: 122°F (50°C)
Clean-In-Place (CIP): 122°F (50°C)
Continuous operation: 3.0-10.0,
Clean-In-Place (CIP): 2.0-10.5
Over an element: 15psi (103kPa)
Per housing: 60 psi (414 kPa)
500+ ppm-hours,
Dechlorination recommended
Pharma Elements
Concentration and Purification of Pharmaceutical Ingredients
The Pharma elements enable the purification and
concentration of high value organic molecules used
in the synthesis of pharmaceutical ingredients.
These elements are used in applications requiring
stringent sanitary procedures.
The Pharma elements feature a patented Durasan*
cage outer wrap, a selection of feed spacers and
polysulfone parts.
The Pharma elements comply with:
• FDA Regulations relevant sections of 21CFR
• EU Framework 1935/2004/EC
Figure 1: Element Dimensions Diagram (Female)
Table 2: Dimensions and Weight
Table 1: Element Specification
1
Average salt rejection after 24h operation. Individual flow rate may vary ±25%.
2
Testing conditions: 2,000ppm NaCl solution at 425psi (2,930kPa) operating pres-
sure, 77°F (25°C), pH6.5 and 15% recovery.
3
Testing conditions: 2,000ppm MgSO4 solution at 110psi (760kPa) operating
pressure, 77 °F (25°C), 15 % recovery.
1
Internal diameter.
² These elements are bagged dry before shipping.
Table 3: Operating and CIP parameter