Hangzhou Winteam Scientific Instruments Co., Ltd.
THE MISSION OF WINTEAM IS PROVIDE BETTER STERILITY TEST PRODUCTION
|Place of Origin:||CHINA|
|Minimum Order Quantity:||ONE BOX|
|Packaging Details:||72sets/box,18sets/box, 48sets/box,12 sets/box|
|Supply Ability:||10000sets per day|
|Name:||Sterility Test Canister||Membrane Material:||MCE NYLON PP|
|Pakcing:||Paper Box||Needle:||304 Stainless Steel|
sterility test kit canister,
sterility test device
sterility test kits pharmaceutical test Single-use closed sterile canister
Characteristics of Sterility Test Canister
Membrane Filtration Method A membrane filtration method generally uses a closed membrane filter. The pore size of the membrane for sterility testing should be no more than 0.45 μm and a diameter of approximately 50 mm. The filter material is selected according to the characteristics of the test sample and its solvent. When used, the integrity of the filter before and after filtration should be guaranteed. A small amount of rinsing liquid should be filtered before the water-soluble test solution is filtered to wet the filter. For oil samples, the filter and filter should be fully dried before use. In order to maximize the filtration efficiency of the membrane, care should be taken to keep the test solution and rinse solution covering the entire surface of the membrane. After the test solution is filtered through the membrane, if it is necessary to rinse the membrane with the rinsing liquid, the amount of each membrane is usually 100 ml per flush, and the total flushing volume should not exceed 1000 ml to avoid microbial damage on the membrane.
|Schematic Diagram||Model||Inspection Style||Packing Spe.|
|Py220C||Glass Bottle Large Volume Injection||
|Ksf220C||Glass Bottle Large-Capacity Antibiotic Injection|
|Kapy220C||Ampoule Antibiotic Injection|
|Dgb220C||Vial Bottle Soluble Powder|
Vial Bottle Soluble Antibiotic Powder
|Sdy220C||Soft Bag Large Volume Injection|
|Nkf220C||Powder That Needs To Be Dissolved And Diluted|
Sterility examination should be carried out under aseptic conditions. The test environment must meet the requirements of sterility inspection. The whole process should be strictly followed by aseptic operation to prevent microbial contamination. Measures to prevent contamination should not affect the detection of microorganisms in the test sample. The unidirectional flow air zone, work surface and environment shall be regularly checked for cleanliness according to the current national standards for test methods for suspended particles, planktonic bacteria and settled bacteria in the clean room (district) of the pharmaceutical industry. The isolation system shall be verified periodically according to the relevant requirements, and the cleanliness of its internal environment shall comply with the requirements of sterility inspection. Daily testing also requires monitoring of the test environment.
Contact Person: wong