• 0.1µm AseptiSure<sup>®</sup> HSR 5", 10", 20", 30"

0.1µm AseptiSure® HSR 5", 10", 20", 30"

mdi AseptiSure® HSR polyethersulfone (PES)membrane cartridge filters are high temperature resistant filtration devices. These are designed to withstand high pressure differential at high steam sterilization temperature upto 135°C. These filters exhibit high mechanical stability, and wide chemical compatibility even with alkaline process fluids.

These filters come with polyethersulfone membrane serial layers and Polypropylene support layers to offer 1-14 pH compatibility.

mdi AseptiSure® HSR 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
Membrane Polyethersulfone
Final Filter Pore Size 0.1µm
Prefilter Pore Size
0.2 µm 0.45 µm
Support Layers Polypropylene
Body and Core Polypropylene
5" 10" 20" 30"
Effective Filtration Area (Nominal)
3000cm² 6000cm² 12000cm² 18000cm²
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
Air Diffusion Flow (5") < 15ml/min @ 50 psi (3.51 Kg/cm²) with Water
Air Diffusion Flow (10") <  29ml/min @ 50 psi (3.51 Kg/cm²) with Water
Max. Operating Temperature 80 °C @ < 2 Kg/cm² (30 psi)
Max. Differential Pressure 3.5 Kg/cm² (50 psi) @ 25 °C
Reverse Pressure <  0.7 Kg/cm² (10 psi) @ 25 °C
Typical Water Flow Rates (10" Cartridge filters) 15 lpm @ 0.70 Kg/cm² @ 27 °C
Sterilization Autoclavable/In-line steam sterilizable at 135 °C for 30 minutes, 25 cycles @ ∆p=5 psi (0.3kg/cm²)
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
Bioburden Bioburden level is < 1000 cfu/filter device as per ISO 11737-1 : 2018
Non Fiber Releasing Passes test as per USP and comply with USFDA 21 CFR Part 210.3(b)(6) for fiber release
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
Particle Shedding The filtrate complies with USP <788> test for particulate matter in injectables.
TOC/Conductivity at 25 °C 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
Quality Management System ISO-9001 Certified
USFDA DMF No. 015554
AseptiSure® HSR (0.2μm Upstream)
AseptiSure® HSR (0.45μm Upstream)
Size Code
5"** 53
10" 54
20" 55
30" 56
Pore Size
Pore Size
0.1µm 36
7P A0
7P without fin A1
28 with fin C0
'O' D0
Silicone SS
Viton SV
FEP Encapsulated Viton FV*
Non Sterile 1
Pack Size
Pack Size Code
1 01

      * FV is available with Adapter code A0 (7P) and A1 (7P without fin) only

      ** Size 5" is available in Adapter Code A0 (7P) and A1 (7P without fin) only

      Example :

CHRX 55 36 A0 SS 1 01
Datasheet Download

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