jainsonsindia partners
 Enquiry Cart

Presterilized PES Membrane Syringe Filters

More Views

Presterilized PES Membrane Syringe Filters

Code:
Presterilized PES Membrane Syringe Filters
PES membrane type LSSYPL-S have Polyethersulfone (PES) membrane filter in a poly-propylene housing. These syringe filters are used for filtration and sterilization of protein solutions, culture media and serum. The low protein binding characteristics make these ideal for these applications, particularly where sample size is very small and recovery of protein of interest is sought.
  • Absolute Retention
  • Low protein binding
  • 16 Channels for minimum back pressure
  • High throughputs
Applications:
  • Sterilization of high value additives such as hormones, vitamins and antibiotics.
  • Sterilization of protein solutions, culture media and buffers
Specifications:
Catalogue No LSSYPL-S 
CONSTRUCTION
Pore size 0.2µm, 0.45µm
Media Polyethersulfone (PES) Membrane
Diameter
4mm 13mm 25mm
Inlet Female luer-lock
Outlet Male luer slip
Housing Polypropylene
OPERATIONAL
Max. Operating Temperature 55 °C
Max. Differential Pressure 75 psi @ 25° C
Burst Pressure >12kg/cm²
Hold-up Volume(with air purge)
<5µl <20µl <50µl
Sterilization Sterilizable by Ethylene Oxide
Effective Filtration Area
0.07 cm² 0.8 cm² 4.15 cm²
Bubble Point (0.2 µm) > 50 psi (> 3.52 Kg/cm²)
Bubble Point (0.45 µm) > 32 psi
Clean Water Flow Rate @ 20 psi (0.2µm)
> 0.8 ml/min > 12 ml/min > 80 ml/min
Clean Water Flow Rate @ 20 psi (0.45µm)
> 4 ml/min > 30 ml/min > 180 ml/min
Sample Volume
<1ml <10ml <100ml
Retention Efficiency (0.45µm) LRV >7 for Sr. marcescens (ATCC 14756) per cm² of filter area
Retention Efficiency (0.2µm) LRV >7 for Br. diminuta (ATCC 19146) per cm² of filter area
ASSURANCE
Fiber Release Complies with USFDA CFR Title 21, Part 210.3(b)(6) and do not requires any initial Flushing.
Particle Release
The filtrate Complies with USP <788> test for particulate matter in injectables.
Indirect Food Additive
The plastic housing material complies with the requirements of USFDA CFR Title 21 Part 177.1520.
Extractables with WFI
Passes test as per USP
Quality Management System
ISO-9001:2008 Certified
 
Description

Details

Presterilized PES Membrane Syringe Filters
PES membrane type LSSYPL-S have Polyethersulfone (PES) membrane filter in a poly-propylene housing. These syringe filters are used for filtration and sterilization of protein solutions, culture media and serum. The low protein binding characteristics make these ideal for these applications, particularly where sample size is very small and recovery of protein of interest is sought.
  • Absolute Retention
  • Low protein binding
  • 16 Channels for minimum back pressure
  • High throughputs
Applications:
  • Sterilization of high value additives such as hormones, vitamins and antibiotics.
  • Sterilization of protein solutions, culture media and buffers
Specifications:
Catalogue No LSSYPL-S 
CONSTRUCTION
Pore size 0.2µm, 0.45µm
Media Polyethersulfone (PES) Membrane
Diameter
4mm 13mm 25mm
Inlet Female luer-lock
Outlet Male luer slip
Housing Polypropylene
OPERATIONAL
Max. Operating Temperature 55 °C
Max. Differential Pressure 75 psi @ 25° C
Burst Pressure >12kg/cm²
Hold-up Volume(with air purge)
<5µl <20µl <50µl
Sterilization Sterilizable by Ethylene Oxide
Effective Filtration Area
0.07 cm² 0.8 cm² 4.15 cm²
Bubble Point (0.2 µm) > 50 psi (> 3.52 Kg/cm²)
Bubble Point (0.45 µm) > 32 psi
Clean Water Flow Rate @ 20 psi (0.2µm)
> 0.8 ml/min > 12 ml/min > 80 ml/min
Clean Water Flow Rate @ 20 psi (0.45µm)
> 4 ml/min > 30 ml/min > 180 ml/min
Sample Volume
<1ml <10ml <100ml
Retention Efficiency (0.45µm) LRV >7 for Sr. marcescens (ATCC 14756) per cm² of filter area
Retention Efficiency (0.2µm) LRV >7 for Br. diminuta (ATCC 19146) per cm² of filter area
ASSURANCE
Fiber Release Complies with USFDA CFR Title 21, Part 210.3(b)(6) and do not requires any initial Flushing.
Particle Release
The filtrate Complies with USP <788> test for particulate matter in injectables.
Indirect Food Additive
The plastic housing material complies with the requirements of USFDA CFR Title 21 Part 177.1520.
Extractables with WFI
Passes test as per USP
Quality Management System
ISO-9001:2008 Certified
 
Additional Information

Additional Information

Code No
Reviews