0.1µm AseptiSure HSR Mini 2.5", 5"
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
- Non-toxic material of construction
- Multiple Autoclave
- Heat sealed, no glues or adhesives
- Each filter comes with an individual certificate of quality
- Total Traceability: Unique identification number is laser etched on each filter
- Sterile Filtration of Culture media for mammalian cell culture
Construction | |||
Membrane | Polyethersulfone | ||
Final Filter Pore Size | 0.1µm | ||
Prefilter Pore Size |
|
||
Support Layers | Polypropylene | ||
Body and Core | Polypropylene | ||
Integrity Testing / Retention | |||
Bubble Point | > 31psi (2.18Kg/cm²) with 50% IPA/Water Solution | ||
Microbial Retention | LRV >7 for Acholeplasma laidlawii (ATCC 23206) per cm² | ||
Size | |||
Size |
|
||
Effective Filtration Area (Nominal) |
|
||
Operational | |||
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 | ||
Typical Water Flow Rates (10" Cartridge filters) |
|
||
Sterilization | Autoclavable/In-line steam sterilizable at 135 °C for 30 minutes, 25 cycles @ Δp= 5psi (0.3kg/cm²) | ||
Assurance | |||
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 |
|
|
|
|
|
|
|
*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 |
Datasheet | Download |