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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ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment

ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment

    • ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment
    • ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment
  • ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment

    Product Details:

    Place of Origin: CHINA
    Brand Name: WINTEAM
    Certification: ISO9001
    Model Number: py330c

    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
    Contact Now
    Detailed Product Description
    Name: Sterility Test Canister Cap: Silicon Rubber
    Membrane Material: MCE NYLON PP SAL: 10^-6
    Condiction: New Apply: Different Canister For Different Sample
    High Light:

    sterility test kit canister

    ,

    sterility testing pump

     

    Single Use Sterility Peristaltic Test Device Pump microbiology lab equipment

     

    Winteam sterility test canister.PDF

    .

     

     

    Sterility test

    The USP <71> sterility test is any specific test capable of maintaining growth against two different types of media (aerobic organisms as well as aerobic and anaerobic organisms). Samples were prepared by direct inoculation or introduced into the medium by membrane filtration. If the media is transparent, the amount of sample required will depend on the type of product being tested and the size of the batch. The sterility test requires a 14 day incubation period. After 14 days of incubation, there was no evidence of microbial growth and the samples were considered sterile.

     

    The Pacific Biology Laboratory Microbiology Laboratory provides sterility testing services for ISO Class 7 sterile kits in ISO 5 layered flood shields.

     

    Available GMP Microbial Aseptic Testing Service

    Bacteriostatic/fungal disease test

    Sterility test

    Direct transfer

    Closed membrane filtration

    Media fill and growth promotion

     

     

    Sterility test

    The sterility test is defined as a test to verify that the product does not contain live microorganisms. Sterility testing is important for medical devices, drugs, preparations, tissue materials, and other materials that claim to be sterile or infeasible.

     

    Sterility Test Canister

     

            The single-use fully enclosed bacteria culture incubator is composed of a protective cap, an air filter, a connector, a cylinder, a filter membrane, a base, a liquid outlet, and a parallel conduit. After more than forty procedures, each process is strictly inspected. 100% of the products pass the integrity test, and the quality traceability and quality are continuously improved according to the requirements of ISO9001 quality system certification. According to the traits and packaging of the inspection products, a variety of microporous membranes with different materials and different structures were selected, and 28 kinds of collection incubators were designed and developed to meet the needs of sterility inspection of various inspection products.

     

    Features

    •  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.
    •  Transparent blister packs conform to international standards.
    •  Transparent composite packaging to reduce packaging waste and reflect environmental protection
    •  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.
    •  Microbial microbial retention, microbial growth (sensitivity) and sterility testing ensure reliable and reliable results of sterility testing.
    •  Filter: bubble point method, bacterial retention test.
    •  Chewing stability test: The culture period is 14 days.

    parameter

     

    Schematic Diagram Model Inspection Style Packing Spe.
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 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
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 1 Apy220C Ampoule Injection
    Apy330C
    Kapy220C Ampoule Antibiotic Injection
    Kapy330C
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 2 Dgb220C Vial Bottle Soluble Powder
    Dgb330C
    Kdgb220C

     

    Vial Bottle Soluble Antibiotic Powder

    Kdgb330C
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 3 Sdy220C Soft Bag Large Volume Injection
    Sdy330C
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 4 Fsy220C Insoluble Liquid
    Fsy330C
    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 5 Nkf220C Powder That Needs To Be Dissolved And Diluted
    Nkf330C

     

    Pharmaceutical industry: sterility inspection and microbial limit inspection of purified water, water for injection, sterile preparations (large infusion, small injection, powder, biological products, blood products, ophthalmic preparations, maintenance liquid, etc.);

    Medical device industry: sterility inspection and microbial limit inspection of purified water, water for injection, syringe, infusion set, blood transfusion device, intravenous catheter, etc.

    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 6

     

    ISO Steritest Canister Peristaltic Test Device Pump Microbiology Lab Equipment 7

    Product rinse sterility test

    Combination product: Product rinse sterility test is only applicable to products with hollow tubes, such as infusion and infusion sets, which are not suitable for soaking and the fluid channel is marked as sterile, this method is easy to operate and requires modification of FTM media with liquid D rinse products, The eluate was membrane filtered and placed in FTM and SCDM. This method is usually not used.

     

     

    Bulk drugs / biopharmaceuticals

    Bulk drugs (API) have been sterilised according to USP 71 prior to release to the manufacturing process.

     

    Bulk biologics are tested for sterility according to 21 CFR 610.12, which requires a medium (FTM) with sample test sizes listed in the document and a capacity of not less than 10 ml.10

     

     

    Interpretation of sterility test results

    Technicians must be trained in growth testing methods during the cultivation process. Growth is determined by observing a medium that is generally transparent and transparent with respect to the light source, and the turbid (turbid) area of ​​the medium indicates the growth of microorganisms. Once growth is detected, the suspect container is tested to confirm that the turbidity present is due to microbes, not due to decomposition of the sample; sometimes, the sample becomes cloudy due to particle shedding or chemical reaction with the medium. After testing, return to the incubator for the remainder of the incubation period. Samples turbid in the medium were transferred and displayed for four days on the 14th day of the test.

    Contact Details
    Hangzhou Winteam Scientific Instruments Co., Ltd.

    Contact Person: wong

    Tel: +8615869109373

    Send your inquiry directly to us (0 / 3000)