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EPM.FG membrane filter cartridges based on hydrophilic PVDF for clarifying, final and biological filtration of liquids

Description

EPM.FG membrane filter cartridges are produced on the basis of the hydrophilized fluoroplastic membrane with the micron rating of 0.2-0.8 μm. Filter сartridges have high throughput and wide chemical compatibility. 

Nominal Dimensions

Filter cartridges

Height (L), mm

Diameter (D), mm

Filter Area (S), m2

125 (5’’)

70

0.4

250 (10’’)

70

0.8

500 (20’’)

70

1.6

750 (30’’)

70

2.4

1000 (40’’)

70

3.2

Capsule filters

Height (L), mm

Diameter (D), mm

Filter Area (S), m2

250 (10’’)

94

0.8

125 (5’’)

94

0.4

60 (2.5’’)

94

0.2

 Operational parameters

Maximal differential pressure for cartridges, MPa

0.5 MPa at 20°C, 0.2 MPa at 80°C

Maximal differential pressure for capsules, MPa

0.4 MPa at 20°C, 0.2 MPa at 60°C

Maximal reverse differential pressure, MPa

0.1 MPa at 20°C, 0.05 MPa at 80°C (cartridges)

Maximal operational temperature, °C

80°C (for cartridges), 60°C (for capsules)

Direct flow wash out

Hot water (up to 95 °C) and chemical agents (pH 3-14)

Autoclaving

121°С, 0.12 MPa, 30 min., 50 cycles (cartridges)

121°С, 0.12 MPa, 30 min., 25 cycles (capsules)

132°С, 0.2 MPa, 30 min., 30 cycles (cartridges)

Steam sterilization

Up to 132°С, 0.2 MPa, 30 min., 20 cycles (cartridges)

* For detailed instructions on wash out and sterilization of cartridges and capsules please contact technical specialists of Technofilter. 

Quality and safety

EPM.FG membrane filter cartridges are produced in accordance with the regulatory technical documents on product quality and are certified for use in the filtration processes of biopharmaceutical solutions. All EPM.FG filter cartridges are subjected to wash out from organic and mechanical impurities with high-purity water and to 100% integrity control.  

Wash out, integrity control, drying, final assembly and packaging of membrane filter cartridges is carried out in special clean rooms (ISO class 5, 6 and 7) according to the classification of clean rooms in the pharmaceutical industry.  

EPM.FG membrane filter cartridges undergo tests for bacterial and toxicological safety, materials used in the construction of filters have a minimal amount of extractable components and are approved for contact with intravenous drugs and food. Safety of filter cartridges is determined by a series of sanitary and chemical tests, and toxicology tests in compliance with GOST R ISO 10993.1-99, GOST R ISO 10993.5-99, GOST R ISO 10993.10-00.

Integrity test 

In the course of testing each membrane filter cartridge is integrity tested by the non-destructive physical method of determination of rate of air passing through the water wetted membrane.

EPM.FG Filter Cartridges ordering information

EPM.FG

045

D1

250

M

Brand

Micron rating

Adapter code

Cartridge height

Application

 

020 = 0,2 μm

045 = 0,45 μm

065 = 0,65 μm

080 = 0,80 μm

 

A (A1), A4, D (D1), B, B (Sl)

100 mm (4”)

125 mm (5”)

250 mm (10”)

500 mm (20”)

750 mm (30”)

1000 mm (40”)

M – medical and biopharmaceutical industry

P – food industry

E – microelectronics industry

KFM.FG Capsules ordering information

KFM.FG

065

K

60

Brand

Micron rating

Connection type

Capsule height

 

020 = 0,2 μm

045 = 0,45 μm

065 = 0,65 μm

K – sanitary flange connection

P – thread tapered  connection

60 mm (4”)

125 mm (5”)

250 mm (10”)


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