The complete sterility test system includes the sterility test pump and sterility testing canisters, which is a closed system to minimize the risk of false positive and negative results, increasing reliability and improving workflow for sterility testing. It has been certified under the ISO 9001 and the ISO 14001. Multiple models have been developed to accommodate different sample properties and packaging types, meeting the needs of various test samples.
Tailin stetility test canisters used in conjunction with a sterility test pump, is widely applicable for sterility test of sterile preparations, including antibiotics and preparations containing bacteriostatic ingredients, sterile APIs, I.V. fluids, aqueous injections, sterilized medical instruments, sterilized WFI, etc.
| Applications | EO Pre-Sterilized | Irradiation Pre-Sterilized | ||
| Pouch Package | Blister Box Package | Pouch Package | ||
| LVP in Bottle | Without Antibiotics | PY2202* | – | PY2202D* |
| PY220 | B-PY220 | PY220D | ||
| Contain Antibiotics | KSF220 | B-KSF220 | KSF220D | |
| Liquid in Ampoule | Without Antibiotics | APY220-P* (for oily product) |
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| APY220 | B-APY220 | APY220D | ||
| Contain Antibiotics | KAPY220 | B-KAPY220 | KAPY220D | |
| Powder in Vial | Without Antibiotics | DGB220 | B-DGB220 | DGB220D |
| Contain Antibiotics | KDGB220 | B-KDGB220 | KDGB220D | |
| Powder in Ampoule | Without Antibiotics | DGA220 | – | DGA220D |
| Contain Antibiotics | KDGA220 | – | KDGA220D | |
| Difficult Soluble Powder in a Vial,with Antibiotics | NKF220 | B-NKF220 | NKF220D | |
| LVP in Collapsible Bag | SDY220 | B-SDY220 | SDY220D | |
| Medical lnstrument with Male Luer Connector | YLQ220* | – | YLQ220D* | |
| Medical lnstrument with Female Luer Connector | YLX220* | – | YLX220D* | |
| Viscous Liquid (biological products) | CN220 | B-CN220 | CN220D | |
| Lyophilized Powder for Injection ( biological products) |
DCN220 | – | DCN220D | |
| Prefilled Syringe | PFS2* | – | PFS2D* | |
| Emulsion or Hard Filtrating Aqueous Samples | – | EVS2 | – | |
| Note: “*” indicates customized model. | ||||
The DGB206 canister is recommended. Pierce the specially designed needle into the vial, start the pump, and pump all the samples to be tested in the container in turn (pausing to avoid inhaling air when changing vials. If the total volume of a batch of samples is less than 100 ml, it is recommended to dilute them appropriately before filtration), and then filtered them to achieve uniform sample distribution in the vials.
The NKFX220 canister is recommended. It adopts a three-needle adapter, and the middle needle is designed for a small vial. Pierce the needles in the vial, start the pump, and invert the dissolution liquid bottle, transferring the diluted liquid to the closed container for the next filtration.
The new canister features significantly enhanced impact, collision, and wear resistance, preventing breakage or leakage even if accidentally dropped. Its fully enclosed 360° protected liquid inlet avoids impact damage and improves hose-connection durability under high pressure. A specialized welding process further strengthens pressure resistance, ensuring safer performance during high-speed, high-pressure filtration without risk of cup deformation. The canister also offers improved transparency and clearer graduation lines, including a new 25 mL mark for membrane wetting, making volume observation easier and more accurate.
Yes. The upgraded canister offers significantly improved chemical compatibility, supporting a wide range of commonly used disinfectants and solvents, including ethanol, isopropanol, methanol, sporicides, benzalkonium chloride (e.g., Zephiran), 35% hydrogen peroxide, formaldehyde, iodine tincture, TH4 disinfectant, acetic acid, DMSO, and acetonitrile. This ensures wider applicability in diverse laboratory and cleanroom workflows.
Tailin adopts double-layer dialysis packaging to enable aseptic depackaging and transfer, reducing material cleaning and disinfection workload while minimizing contamination risks. The inner soft blister tray enhances product protection, and the outer composite-film dialysis pouch provides an additional safety barrier. Both layers are made from DuPont™ Tyvek®, whose high mechanical strength ensures packaging integrity, excellent breathability supports sterilization effectiveness, and superior bacterial-barrier properties maintain sterility throughout the product’s shelf life
