Containment Isolator Dealers in Thane

• Item Code: 011
• Application: Pharmaceuticals & Hospital
• Material: PVC 100%,PU,PE
• Condition: New

  containment barrier isolator (cbi):-   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.   features:   ø  controls exposure/cross-contamination risk to hazardous/aseptic materials for a wide variety of equipment and processes   ø  controls false-positive risk for sterility testing   ø  provides operator exposure levels (oel’s) ≤1.0 μg/m3 during controlled operations   ø  levels of ≤0.1 μg/m3 can be achieved via closed-transfer processes or based on client sops   ø  enhances cgmp practices   ø  quiet, energy-efficient ecm fans auto adjust to compensate for filter blockage   ø  standard dimensions available are easily customized to suit process requirements   ø  safe glove change and low contamination filter change   ø  fda-approved static seals   ø  pressure tested class 2 iso 10648-2 standards   ø  system comes with a semi-automated or automated pressure hold testing   ø  pass chamber comes in 2 sizes:   v  small, non-gloved   v  large, non-gloved/gloved   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   containment barrier isolator (cbi):-   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.   features:   ø  controls exposure/cross-contamination risk to hazardous/aseptic materials for a wide variety of equipment and processes   ø  controls false-positive risk for sterility testing   ø  provides operator exposure levels (oel’s) ≤1.0 μg/m3 during controlled operations   ø  levels of ≤0.1 μg/m3 can be achieved via closed-transfer processes or based on client sops   ø  enhances cgmp practices   ø  quiet, energy-efficient ecm fans auto adjust to compensate for filter blockage   ø  standard dimensions available are easily customized to suit process requirements   ø  safe glove change and low contamination filter change   ø  fda-approved static seals   ø  pressure tested class 2 iso 10648-2 standards   ø  system comes with a semi-automated or automated pressure hold testing   ø  pass chamber comes in 2 sizes:   v  small, non-gloved   v  large, non-gloved/gloved   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