Safesure AFB Sterilizing-Grade Bricap C Series Capsule Filters 0.2μm, Gas Filtration
Regular price
$69.00 USD
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*Not for medical use
Specifications
Materials | Membrane | Hydrophobic Polytetrafluoroethylene(PTFE) |
Support | Polypropylene(PP) | |
Core/Cage/End Cap | Polypropylene(PP) | |
Capsule Housing | Polypropylene(PP) | |
Capsule Vent O-rings | Silicone | |
Filtration Area | C01-180cm² C02-420cm² C03-970cm² |
|
Operating Conditions | Max. Operating Temperature | 80°C |
Max. Differential Pressure (Forward) | 0.55 MPa @25°C 0.10 MPa @80°C |
|
Max. Differential Pressure (Reverse) | 0.21 MPa @25°C |
|
Quality Standards | Integrity | 100% Integrity testing |
Traceability | Each filter with a unique serial number | |
QMS | ISO 9001:2015 | |
Sterility | Delivery Condition | Non-sterile |
Sterilization Method | Can be autoclaved 50 cycles for 30 minutes at 130°C (Can not be steam sterilized in-line) | |
Package | Pack Size | 1/pk |
Packaging | Double PE bag |
*Note: Cobetter also provides filters with different sterilization methods:
Sterile Breathable Bag Package: Pre-sterilized filters by autoclaved for 30 minutes at 121°C.
Features
- PTFE is inherently hydrophobic and further processed for even more hydrophobic, maintaining sterilizing capacity in both unwet and wet condition
- Oleo-phobic
- High retention rates, low-pressure differential
- Use of heat-resistant thickened PP as core, better heat resistance and pressure resistance
- Heat resistance, can be steamed in line and autoclaved repeatedly
Applications
- Vent filter for fermentation, storage tanks
- Sterile filtration for compressed air, oxygen, nitrogen
- Single-use system application
Regulatory Compliance
- Effluent meets the USP<788> requirement of particulate matter in large volume injection.
- Component materials meet the criteria for a “Non-fiber-releasing filter”as defined in 21 CFR 210.3(b)(6).
- Retention of 10⁷ cfu/cm² Brevundimonas diminuta(ATCC 19146) according to ASTM F838.
- Typical Log Reduction Value (LRV) >7 of Acholeplasma laidlawii (ATCC 23206) according to ASTM F838
- Aqueous extraction from a cartridge contains less than 0.25EU/ml as determined by Limulus Amebocyte Lysate (LAL), meeting requirements of USP<85>.
- Components meet the requirement of USP <87> In Vitro Biological Reactivity Test.
- Components meet the criteria of the USP <88> Biological Reactivity Test for Class V-121 °C plastics.
- Components meet the FDA indirect Food Additive requirements cited in 21 CFR177-182.
- Based on the current information from our suppliers, all components used in the manufacture of this product are animal-free.
*Contact us for more specification details.