0.1µm AseptiSure® HSR Mini
MDI AseptiSure® HSR polyethersulfone (PES) membrane mini cartridge filters are designed to withstand high pressure differential upto 0.3 Kg/cm² (5 psi) at high steam sterilization temperatures of up to135 °C.
These filters with polyethersulfone membrane and polypropylene support layers offer pH compatibility from 1 to14, and are thus ideal for use with acidic as well as alkaline solutions.
MDI AseptiSure® HSR mini cartridge filters are validated for key performance parameters such as retention efficiency, chemical compatibility, extractables, heat stability and flow rates.
- Low protein binding
- High throughputs
- Long service life
- Pre-flushed to minimize particulate release after installation
- Non-toxic material of construction
- Multiple autoclavable/SIP
- Absolute retention
- 100% integrity tested
- High flow rates
- Bioburden maintained below 1000 cfu/device
- Endotoxin level certified to be <0.25 EU/ml
- Unique identification number is laser etched on each filter
- Individual certificate of quality for each device
- Sterilizable by Autoclaving/Steaming in place (SIP)
- Sterile Filtration of Culture media for mammalian cell culture
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| Membrane | Polyethersulfone | ||
| Final Filter Pore Size | 0.1µm | ||
| Prefilter Pore Size |
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| Support Layers | Polypropylene | ||
| Body and Core | Polypropylene | ||
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| Effective Filtration Area (Nominal) |
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| Bubble Point | > 26 psi (1.82 Kg/cm²) with 50% IPA
> 65 psi (4.56 Kg/cm²) with Water |
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| Microbial Retention | LRV >7 for Acholeplasma laidlawii (ATCC 23206) per cm² | ||
| Max. Operating Temperature | 80 °C @ < 2 Kg/cm² (30 psi) | ||
| Max. Differential Pressure | 3.5 Kg/cm² (50 psi) @ 25 °C | ||
| Reverse Pressure | < 10 psi (0.7Kg/cm²) @ 25°C | ||
| Sterilization | Autoclavable/In-line steam sterilizable at 135 °C for 30 minutes, 25 cycles | ||
| Toxicity | Passes Bioreactivity test, In Vivo, as per USP <88> for Class VI plastics | ||
| Cytotoxicity | Passes Biological Reactivity Tests, In Vitro, USP <87> for cytotoxicity | ||
| Bacterial Endotoxin | Aqueous extracts exhibit < 0.25 EU/ml as established by Limulus Amebocyte Lysate (LAL) Test | ||
| Non Fiber Releasing | Passes test as per USP and comply with USFDA 21 CFR Part 210.3(b)(6) for fiber release | ||
| TOC and Conductivity | Meets the WFI requirements of USP <643> for Total Organic Carbon and USP <645> for Water Conductivity after a specified volume of purified water flush | ||
| Particle Release | The filtrate complies with USP <788> test for particulate matter in injections | ||
| Indirect Food Additive | All Polypropylene components meet the FDA Indirect Food Additive requirements cited in 21 CFR 177.1520 | ||
| Extractables with WFI | Passes test as per USP | ||
| Good Manufacturing Practice | These products are manufactured in a facility which adheres to Good Manufacturing Practices. | ||
| Oxidizable Substances | Within limits as specified in USP | ||
| Quality Management System | ISO-9001 Certified | ||
| USFDA | DMF No. 015554 | ||
| Typical Water Flow Rates (10″ Cartridge filters) |
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*G0 adapter code is not available with any elastomer. Please mention XX in place of elastomer code while ordering
**Adapter code F0 is available only in 5” cartridge filters
Example :
| CHRX | 50 | 36 | E0 | SS | 1 | 01 |
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