sterility test kits pharmaceutical test Single-use closed sterile canister

Characteristics of Sterility Test Canister

• Assembled clamps for pipelines are more convenient to use;
• Double-layer aseptic packaging facilitates the transfer in the clean room and reduces the pollution during the transfer process;
• Transparent blister packs conform to international standards.
• Transparent composite packaging to reduce packaging waste and reflect environmental protection
• Produces in 10,000 grade level clean room
• Composite membrane packaging technology, great breathability and bacteria resistance.
• Ultrasonic welding technology, ensures leakproofness and withstands pressure.

Sterility testing is an extremely important step in the release of sterile products. False positives, false negative test results, and laboratory equipment failures and human error will bring a lot of time and money to the customer and directly affect the final release of the product. The collection of YT series of bacterial collection equipment and sterile culture equipment provides the perfect solution. The test sample pump in different packaging forms is safely and evenly transferred to the collection incubator by the peristaltic collection instrument pump, so that the sterility test result is more consistent and reliable.

parameter

 

Schematic Diagram	Model	Inspection Style	Packing Spe.
	Py220C	Glass Bottle Large Volume Injection	72Sets/Box 18sets/Box   48 Sets/Box 12sets/Box
	Py330C
	Ksf220C	Glass Bottle Large-Capacity Antibiotic Injection
	Ksf330C
	Apy220C	Ampoule Injection
	Apy330C
	Kapy220C	Ampoule Antibiotic Injection
	Kapy330C
	Dgb220C	Vial Bottle Soluble Powder
	Dgb330C
	Kdgb220C	Vial Bottle Soluble Antibiotic Powder
	Kdgb330C
	Sdy220C	Soft Bag Large Volume Injection
	Sdy330C
	Fsy220C	Insoluble Liquid
	Fsy330C
	Nkf220C	Powder That Needs To Be Dissolved And Diluted
	Nkf330C

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.