25 mm Acrylic Syring Disk Fluid Filter 0.2 Micron Pore Size With Supor membrane, clear/blue, FLL/MLL, sterile Superior flow rates and throughput offer faster filtration times and more filtration per device Biologically safe - all materials of construction pass USP Biological Reactivity Tests, In Vivo <88> Effective Filtration Area 2.8 cm2 Maximum Operating Pressure 5.2 bar (75 psi) 50 Units Per box
Product Design and Performance Advantages
Customer Qualified Applications
• Pharmacy Admixture
• Small Volume Sterilisation
• Low volume pain control
• Low volume injectables
Materials of Construction Filter Membrane: Supor Polyethersulfone, Versapor Acrylic Copolymer membrane and Polyester Screens Filter Housing: Modified Acrylic Biological Safety Materials of construction have been evaluated in accordance with United States Pharmacopeia (USP) Biological Reactivity Tests, In Vivo <88> (USP Class VI-121 oC Plastic tests) and/or relevant sections of the ISO 10993 series of standards. Material Content Declaration Materials of construction do not contain: - Natural latex or latex derivatives - PVC or hydroxyvinyl chloride - DEHP- Diethylhexylphthalate - BPA - Bisphenol A - TSE - Transmissible spongiform encephalopathy - BSE - Bovine spongiform encephalopathy Effective Filtration Area/ EFA Approx. 2.8 cm2
Pyrogenicity < 0.25 EU/mL using the LAL test method Inlet/Outlet Connectors FLL: Female Luer Lock MLL: Male Luer Lock MLS: Male Luer Slip Water Bubble Point Supor Membrane: 0.2 µm: ≥ 3.1 bar (46 psi) 5.0 µm: ≥ 0.2 bar (3 psi) Versapor: 5.0 µm: ≥ 0.034 bar (0.5 psi) (≥ 1.0” Hg) Retention properties 0.2 µm Supor membrane is retentive of B.diminuta and meets requirements for a sterilizing grade filter per modified ASTM F838-15a test methods Sterilization Compatibility Ethylene Oxide or Gamma irradiation Water Flow rate Supor Membrane: 0.2 µm: ≥ 180 mL/min at 3.1 bar (45 psi) 5.0 µm: ≥ 1500 mL/min at 3.1 bar (45 psi) Versapor: 5.0 µm: ≥ 970 mL/min at 3.1 bar (45 psi
Product Design and Performance Advantages
Customer Qualified Applications
• Pharmacy Admixture
• Small Volume Sterilisation
• Low volume pain control
• Low volume injectables
Materials of Construction
Filter Membrane: Supor Polyethersulfone, Versapor
Acrylic Copolymer membrane and Polyester Screens
Filter Housing: Modified Acrylic
Biological Safety
Materials of construction have been evaluated in
accordance with United States Pharmacopeia (USP)
Biological Reactivity Tests, In Vivo <88> (USP Class
VI-121 oC Plastic tests) and/or relevant sections of the
ISO 10993 series of standards.
Material Content Declaration
Materials of construction do not contain:
- Natural latex or latex derivatives
- PVC or hydroxyvinyl chloride
- DEHP- Diethylhexylphthalate
- BPA - Bisphenol A
- TSE - Transmissible spongiform encephalopathy
- BSE - Bovine spongiform encephalopathy
Effective Filtration Area/ EFA
Approx. 2.8 cm2
Pyrogenicity
< 0.25 EU/mL using the LAL test method
Inlet/Outlet Connectors
FLL: Female Luer Lock
MLL: Male Luer Lock
MLS: Male Luer Slip
Water Bubble Point
Supor Membrane: 0.2 µm: ≥ 3.1 bar (46 psi)
5.0 µm: ≥ 0.2 bar (3 psi)
Versapor: 5.0 µm: ≥ 0.034 bar (0.5 psi) (≥ 1.0” Hg)
Retention properties
0.2 µm Supor membrane is retentive of B.diminuta
and meets requirements for a sterilizing grade filter per
modified ASTM F838-15a test methods
Sterilization Compatibility
Ethylene Oxide or Gamma irradiation
Water Flow rate
Supor Membrane: 0.2 µm: ≥ 180 mL/min at 3.1 bar (45 psi)
5.0 µm: ≥ 1500 mL/min at 3.1 bar (45 psi)
Versapor: 5.0 µm: ≥ 970 mL/min at 3.1 bar (45 psi