ClariCap® GS Inline
MDI ClariCap® GS Microglassfiber Capsule Filters are multilayered, high throughput filters, specially designed for turbid and difficult to filter solutions. The microglassfiber medium is designed to retain colloidal particles and for removal of deformable and nondeformable particles and microorganisms from liquids.
The polypropylene layer downstream of microglassfiber layers prevents media migration. The high dirt holding capacity, biochemical inertness, adsorption and high wet strength of the filtration medium makes it suitable for clarification and prefiltration of wide range of aqueous, non-aqueous and biologicals solutions.
- Very high particulate retention efficiency
- High throughput
- High heat resistance
- Wide chemical compatibility
- No media migrating
- Biologically inert
- Easy installation
- Endotoxin level certified to be <0.25 EU/ml
- Widest range of end connections
- Products available for total scalability from a few ml to thousands of liters
- Sterilizable by Autoclaving or Ethylene Oxide
- Pre-filtration of high value difficult to filter drug solutions
- Precipitate removal in protein processing and plasma fractions
- Removal of un-dissolved buffer salts and cell culture media
- Prefiltration of serum and other viscous biologicals
- Polishing of turbid solution
- Chemical Processing
- Beverage clarification
| Construction | |||
| Pore size | 0.7µm, 1µm, 1.5µm,2µm | ||
| Filter Media | Multilayered Microglassfiber | ||
| Body and Core | Polypropylene | ||
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| Operational | |||
| Max. Operating Temperature | 60 °C | ||
| Max. Differential Pressure | 3Kg/cm² (42 psi) @ 30 °C | ||
| Sterilization By Gas | Sterilizable by Ethylene Oxide | ||
| Sterilization By Autoclave | Autoclavable at 125°C for 30minutes, 30 cycles and it cannot be in-line steam sterilized | ||
| Shelf Life | 3 years after EO sterilization | ||
| Assurance | |||
| Toxicity | Passes Bioreactivity test, In Vivo, as per USP <88> for Class VI plastics | ||
| Bacterial Endotoxin | Aqueous extracts exhibit < 0.25 EU/ml as established by Limulus Amebocyte Lysate (LAL) Test as per USP <85> | ||
| 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 | ||
| 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 | ||
| Good Manufacturing Practice | These products are manufactured in a facility which adheres to Good Manufacturing Practices | ||
| Oxidizable Substances | Within limits as specified in USP <1231> | ||
| Particle Shedding | Passes USP test for particulates in injections | ||
| Quality Management System | ISO-9001 Certified | ||
| USFDA | DMF No. 015554 | ||
ClariCap® GS- 25mm
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*Female Luer Lock is available as Inlet only
**Male Luer Slip is available as Outlet only
Example :
| IGKX | 06 | 05 | MN | X | X | 1 | 04 |
Example for Non Sterile: IGSX0605MNXX104 Example for EO Sterile: IGSX0605MNXX204
ClariCap® GS- 50mm
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*¼” Stepped Hose Barb and ¾” Sanitary Flange are available in filters with vent only
**¼” Single Step Hose Barb and Female luer lock is available in filters without vent only
Example :
| VGSX | 10 | 05 | BB | X | X | 1 | 02 |
Example for Non Sterile: VGSX1005BBXX102 Example for EO Sterile: VGSX1005BBXX202
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