1 Sales HJ-ORABS sterile isolator,Manufacturer

HJ-ORABS sterile isolator

Product ID:SHGCglq024

Price: Please inquire PDF Format
Supply Ability:20SETS/MON
Port:SHENZHEN
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  • Product Introduction
  • Consulting
  • Model NumberHJ-ORABS
    Brand NameSZGYYQHJJJKJ
    Payment TermsT/T, paypal
    Function introduction:
    Aseptic isolation system (isolator) is A kind of vertical unidirectional flow air purification equipment, which provides A local class A environment and human machine separation. It is widely used in the pharmaceutical industry to create A class A fully enclosed clean environment in the context of low-level clean environment.
    Product features:
    Double-door transfer technology: ensure clean space is not affected by material transfer and personnel operation, and solve the problem that traditional sterile room grade 100 cleanliness cannot be maintained continuously;
    Monitoring system: the operating parameters of the isolator, such as pressure, temperature, humidity and cleanliness, are monitored online, which conform to GMP/GLP management requirements.
    Control system: automatic control of microcomputer;
    Positive and negative pressure can be adjusted to meet the protection requirements of toxic substances and prevent pollution;
    The cabin can be moved: it is easy to be moved and installed and can reduce the requirements of external environment and save cost.
    Sterilization mode: ozone or gasification hydrogen peroxide modes are available.
    Technical parameters:
    Cleanliness: Class A
    Average wind speed: 0.36~0.54m/s
    Air current: vertical flow
    Noise: 60 db or less
    High efficiency filter: DOP, filtering efficiency is greater than 99.997%
    Dimensions: customized according to customer requirements
    Disinfection system: VHP



     
  • Function introduction:
    Aseptic isolation system (isolator) is A kind of vertical unidirectional flow air purification equipment, which provides A local class A environment and human machine separation. It is widely used in the pharmaceutical industry to create A class A fully enclosed clean environment in the context of low-level clean environment.
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