Hangzhou Winteam Scientific Instruments Co., Ltd.

Hangzhou Winteam Scientific Instruments Co., Ltd.

THE MISSION OF WINTEAM IS PROVIDE BETTER STERILITY TEST PRODUCTION

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304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization

304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization

  • 304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization
  • 304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization
  • 304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization
Product Details:
Place of Origin: CHINA
Brand Name: WINTEAM
Certification: ISO9001
Model Number: KSY
Payment & Shipping Terms:
Minimum Order Quantity: ONE BOX
Price: Negotiable
Packaging Details: 72sets/box,18sets/box, 48sets/box,12 sets/box
Supply Ability: 10000sets per day
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Detailed Product Description
Name: Sterility Test Canister Membrane Material: MCE NYLON PP
Pakcing: Paper Box Needle: 304 Stainless Steel
Usage: Filteration Power Supply: AC220V/50Hz
High Light:

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.

 

parameter

 

Schematic Diagram Model Inspection Style Packing Spe.
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 0 Py220C Glass Bottle Large Volume Injection

72Sets/Box

18sets/Box

 

48 Sets/Box

12sets/Box

Py330C
Ksf220C Glass Bottle Large-Capacity Antibiotic Injection
Ksf330C
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 1 Apy220C Ampoule Injection
Apy330C
Kapy220C Ampoule Antibiotic Injection
Kapy330C
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 2 Dgb220C Vial Bottle Soluble Powder
Dgb330C
Kdgb220C

 

Vial Bottle Soluble Antibiotic Powder

Kdgb330C
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 3 Sdy220C Soft Bag Large Volume Injection
Sdy330C
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 4 Fsy220C Insoluble Liquid
Fsy330C
304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 5 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.

 

304 SS Sterility Testing Pump , Sterility Test Closed Canister Gamma Ray Sterilization 6

 

 

Contact Details
Hangzhou Winteam Scientific Instruments Co., Ltd.

Contact Person: wong

Tel: +8618968055427

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