
Models and specifications
STI-1200
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 1600*880*2250 |
Operation cabin Size(W*D*H)mm | 1195*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1200/BPB600
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 1600*880*2250 |
Operation cabin Size(W*D*H)mm | 1195*680*700 |
Size of transfer cabin(w*D*H)mm | 600*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1500D/BPB600
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 2100*1200*2250 |
Operation cabin Size(W*D*H)mm | 1195*680*700 |
Size of transfer cabin(w*D*H)mm | 600*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1800
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 2200*880*2250 |
Operation cabin Size(W*D*H)mm | 1795*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1800/BPB600
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 2200*880*2250 |
Operation cabin Size(W*D*H)mm | 1795*680*700 |
Size of transfer cabin(W*D*H)mm | 600*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1800D/BPB600
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 2200*1200*2250 |
Operation cabin Size(W*D*H)mm | 1795*1195*700 |
Size of transfer cabin(W*D*H)mm | 600*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
STI-1800/PB600
Product Introduction
The sterile isolator is a closed-type operating device designed to provide a localized Class A clean environment, primarily used for aseptic operations, microbial control, and the protection of operators or products from contamination. It is widely applied in pharmaceuticals, biotechnology, healthcare, and laboratory settings—particularly in scenarios such as sterile pharmaceutical production, cell culture, and manipulation of highly pathogenic microorganisms. The isolator employs hydrogen peroxide vapor (VHP) sterilization technology to comprehensively sterilize the chamber, achieving a kill rate of up to 6-log. By integrating a HEPA/ULPA filtration system, a sealed chamber design, and glove-based operations, the device ensures that the operating environment complies with regulatory requirements, including GMP and ISO 14644-1 standards.
Technical parameter
project | technical parameter |
Overall dimension(W*D*H)mm | 1600*880*2250 |
Operation cabin Size(W*D*H)mm | 1195*680*700 |
Size of transfer cabin(W*D*H)mm | 600*680*700 |
Compressed air volume | ≥0.6Mpa |
Work area cleanliness | Class A |
Air supply velocity | 0.36-0.54 m/s |
noise | ≤75dB(A) |
illuminance | >300Lux |
power | 4KW |
Power Supply Voltage | AC220V±10%,50Hz±1Hz |
control model | Manual mode, Automatic mode |
Door sealing method | Inflatable sealing |
sterilization method | Vaporized hydrogen peroxide |
Sterilization efficiency | 6lg |
Automatic sterilization duration | <240 min |
Concentration of hydrogen peroxide after residual removal | <1PPM |
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