0.22μM Air Filter Sterility Testing Unit , Closed Sterile Canister Complete Detection
NKF330C Sterility Test Device for sterility test canister 0.45μm filter membrance
Sterility Test Canister
Sterility testing is an extremely important step before the release of sterile products. False-positive, false-negative experimental results, as well as experimental equipment failures and human error can cause significant time and money losses to the customer and directly affect the laboratory performance of the product. The combination of the Ai series collection instrument and the collection culture incubator provides a perfect solution. The test samples of different packaging forms are safely and uniformly transferred to the collecting culture incubator by the peristaltic pump of the collecting instrument, so that the sterility test results are more consistent and reliable.
Features
- Two layers of aseptic packaging facilitate cleanroom transfer and reduce contamination during transfer.
- Gamma sterilization, no residue, safe and reliable, to avoid false negative results.
- SAL 10 10-6, in line with the requirements of the 2015 Chinese Pharmacopoeia radiation sterilization method.
- Filter: bubble point method, bacterial retention test.
- Chewing stability test: The culture period is 14 days
- Ultrasonic welding process, the welding is smooth and sturdy, to achieve the best sealing performance.
- The elastic high-elastic pump tube is made of special materials and has long-term durability, wear resistance and pressure resistance to ensure complete detection.
- Imported medical dialysis packages from the United States can be used to rapidly degrade ethylene oxide and reduce ethylene oxide residues to ensure product sterility.
- Transparent blister packs conform to international standards.
- Transparent composite packaging to reduce packaging waste and reflect environmental protection
- Microbial microbial retention, microbial growth (sensitivity) and sterility testing ensure reliable and reliable results of sterility testing.
- Filter: bubble point method, bacterial retention test.
parameter
| Schematic Diagram | Model | Inspection Style | Packing Spe. |
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Py220C | Glass Bottle Large Volume Injection |
72Sets/Box 18sets/Box
48 Sets/Box 12sets/Box |
| Py330C | |||
| Ksf220C | Glass Bottle Large-Capacity Antibiotic Injection | ||
| Ksf330C | |||
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Apy220C | Ampoule Injection | |
| Apy330C | |||
| Kapy220C | Ampoule Antibiotic Injection | ||
| Kapy330C | |||
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Dgb220C | Vial Bottle Soluble Powder | |
| Dgb330C | |||
| Kdgb220C |
Vial Bottle Soluble Antibiotic Powder |
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| Kdgb330C | |||
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Sdy220C | Soft Bag Large Volume Injection | |
| Sdy330C | |||
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Fsy220C | Insoluble Liquid | |
| Fsy330C | |||
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Nkf220C | Powder That Needs To Be Dissolved And Diluted | |
| Nkf330C |
100% of the products pass the integrity test, achieving continuous improvement of quality traceability and quality. According to the testing requirements of different dosage forms and packaging forms, a variety of different cup materials, filter materials and matching needles were selected, and a variety of collection incubators were designed and developed to meet the sterility inspection of various samples. need.
In addition, there are are operating videos for our products for the convenience of customers to use.

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