The VentiLink® Series ESG Hydrophobic Filters from BioLink are gammairradiatable filtration units which can be integrated into single-use sterile assemblies.
The VentiLink® Series ESG Filters with 0.2 μm sterilizing-grade hydrophobic polyethylene (PE) membranes can be widely used in gas filtration applications, offering excellent throughput with low differential pressure and high flow rate.
The VentiLink® series offers disc capsules for R&D stage, large capsules for commercial production, supporting applications from drug development, pilot scale to commercial manufacturing.
| Product Series | Filtration Grade | Membrance Code | Membrance Pore Size (μm) | Min. Bubble Point (@22°C) |
| VentiLink® Series ESG Hydrophobic Filters | Sterilizing grade | ESG02 | 0.2 | 1.2 bar (in 60% isopropanol, 40% purified water) |
Single-use bioprocessing bag gas intake/vent
Bottles or Carboy aspirators
Compressed gas filtration
Excellent Performance
Validated high-quality hydrophobic polyethylene (PE) membrane
High throughput, low differential pressure, long shelf life
Easy wetting for rapid integrity testing
Full range of specifications for easy scale-up
Regulatory Compliance
Designed, developed and manufactured under an ISO 13485-certified quality management system
100% integrity test
Each filter is supplied with a quality certificate
Each filter and its packaging come with a conformity certificate, part number, batch number, and identification label for full traceability and easy identification
Comprehensive validation guide documentation available
Category | Test Item | Standard/Test Result |
Bacterial retention | Bacterial retention capability | Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta per ASTM methodology. Membrane bubble point test data is correlated to bacterial challenge test results |
Physiochemical | TOC | Meets current USP requirements for purified water |
Conductivity | Meets current USP requirements for purified water | |
Oxidizable substances | Meets current USP requirements for oxidizable substances | |
Cleanliness | Particulate matter | The microscopic count of the filtrate meets the current USP requirements for particulate matter in injections |
Bacterial endotoxin | <0.25 EU/mL, meets current USP requirements for bacterial endotoxin | |
Nonfiber-releasing | Meets 21 CFR 211.72 and 210.3 (b) (6) nonfiber-releasing requirements | |
Safety | ADCF | No animal-derived components were added or used |
REACH | Complies with REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) Article 57 and Regulation No. 1907/2006 | |
Material toxicity | Non-toxic, complies with Restriction of Hazardous Substances (RoHS 3) Directive 2015/863 | |
Biocompatibility | Passes current USP Class VI-121°C plastic testing; Tested per current USP MEM elution method, with no potential cytotoxicity | |
Indirect food additive | Meets FDA 21 CFR 177 requirements for Indirect food additives |
| oduct Series (Membrane Type) | Filter Type |
VentiLink® Series
| CapsHub® G Series Disc Capsules |
CapsHub® SG Series Capsules | |
CapsHub® MG Series Capsules | |
CapsHub® LG Series Large Capsules |
Specification | G13 | G25 | G40 | G50 | |
Size (mm) | Body diameter | 16 | 33 | 45.5 | 55 |
Body length without fittings | 3.7 | 5.45 | 8 | 8 | |
Effective Filtration Area (cm²) | 0.8 | 4.6 | 10.5 | 15.9 | |
Structure and Material | Filter membrane | Polyethylene (PE) | Polyethylene (PE) | Polyethylene (PE) | Polyethylene (PE) |
Support | NA | NA | NA | Polyethylene (PE) | |
Cage | Polyethylene (PE) | Polyethylene (PE) | Polyethylene (PE) | Polyethylene (PE) | |
Operating Parameters | Max. working temperature | 55℃ | 55℃ | 55℃ | 55℃ |
Max. inlet pressure (22°C) | 2.1bar | 2.1bar | 2.1bar | 4.1bar | |
Max. forward differential pressure (22°C) | 2.1bar | 2.1bar | 2.1bar | 2.1bar | |
Sterilization Conditions | Gamma irradiation: up to 50kGy | ||||
Link With Us Now!