technology

right Chemistry See all product

Containment Barrier Isolator

☆☆☆☆☆ ( 0 rates ) 152
Price : Call

Code: #19107

Supplier: Esco Micro Pte. Ltd.

Applications

  • Pharmacy Compounding (Chemotherapy/TPN)
  • As a Class III Cabinet for Biosafety Levels (BSL) 3 and 4
  • Small Batch Sterility Testing
  • Small-scale Potent Material Handling
  • Cell Processing
  • Aseptic Processing
  • Research and Development

rightMORE INFORMATION

  • Esco Containment Barrier Isolator (CBI) facilitates the isolation of a product or process while providing the required conditions for a sterile/aseptic environment. It is configured to operate at positive or negative pressure. This equipment provides a comprehensive range of personnel and product protection in addition to protection for the surrounding work areas and the environment.

    CBI's design has complete compliance to PIC/s and EU cGMP standards with its 19 mm radius coved internal corners in a single piece chamber (no perforations or grilles for contaminants to be trapped on all 4 corners). Its Rear Return Filter ensures that ducts are not contaminated. The system comes in either recirculatory or single pass airflow.

  • Isolator

    Code

    Airflow Regime

    Code

    Internal Width

    No. of Glove Ports

    Pass-through Chamber

    Code

    Electrical Code

    Containment Barrier Isolator

    CBI

    Unidirectional

    U

    1200 mm

    2G

    1 Pass-through chamber

    1PTC

    220-240 V, AC, 50 Hz, 1Ø

    Turbulent

    T

    1600 mm

    3G

    2 Pass-through chamber

    2PTC

    110-120 V, AC, 50 Hz, 1Ø

      

    2000 mm

    4G

     

     

     

    • Controls exposure/cross-contamination risk to hazardous/aseptic materials for a wide variety of equipment and processes
    • Controls false-positive risk for sterility testing
    • Provides Operator Exposure Levels (OEL’s) ≤1.0 μg/m3 during controlled operations
    • Levels of ≤0.1 μg/m3 can be achieved via closed-transfer processes or based on client SOPs
    • Enhances cGMP practices
    • Quiet, energy-efficient ECM fans auto adjust to compensate for filter blockage
    • Standard dimensions available are easily customized to suit process requirements
    • Safe glove change and low contamination filter change
    • FDA-approved static seals
    • Class 2 containment enclosure on manual pressure leak test and Class 3 containment enclosure on automated pressure test as per ISO 10648-2
    • System comes with a Semi-automated or Automated Pressure Hold Testing
    • Pass Chamber comes in 2 sizes:
      • Small, non-gloved
      • Large, non-gloved/gloved

 
Scroll