Summary: Test isolator used in QC laboratory asepsis, microbial limit test. Aseptic test isolator is composed of test chamber, integrated bacteria collector, VHP sterilizer and necessary test port. Positive or negative pressure (used to protect the safety of drugs or operators) in the cabin. Sterile and microbial limit inspection, the sample (with packaging container), test equipment, culture medium and buffer incoming lab, pay attention to ensure that the sample (with packaging container), test equipment, fully exposed, such as medium and buffer can be through a dedicated sterilization, the optimum effect of sterilization, start the sterilization procedures VHP sterilization (sterilization) was carried out on the surface of microbes, after the sterilization, hold hydrogen peroxide residue after reaching safety levels, again through the gloves mouth inspection and microbial limit examination of aseptic operation. The laboratory chamber is equipped with a microbiometer for sterility test and microbial limit test. After the inspection, the isolator is sent through the external door. Main technical parameters: Power supply: AC220V plus or minus 22V/50Hz; Power: 500W (tentative); Noise: no more than 65dB (A); Pressure difference: 0 ~ 80Pa (adjustable); Cleanliness: class A (static); Dimensions: 1860mm x 1100mm x 1900mm Differential pressure resolution: 0.1pa The temperature resolution: 0.1 ℃ Humidity resolution: 0.1% RH hour leakage rate: Q/V is less than or equal to 0.5% High efficiency filter: EU14 (counting method); Features: Description of basic functions and features PLC programmable controller program automatic control; Human - machine dialogue interface of touch liquid crystal screen, humanized design; Third level administrator password access; Computer telecommunication function (optional); UBS interface data export and print function; Automatic and manual operation mode; Temperature, humidity and pressure difference monitoring function; Pressure loss alarm function (audible and visual signals); Lighting in the cabin: luminance greater than or equal to 300lx (cold light source); Waterproof and sterile socket in the cabin (company patent); The detection orifice of particle, plankton and sedimentation is reserved. Reserve sterilization interface (the buyer provides basic parameter information); Reserve the in-place cleaning interface (the buyer provides basic parameter information); Reserve the DOP test port of the high efficiency filter (the buyer provides basic parameter information); Function of catalytic decomposition of sterilizer (optional by user);
Summary: Test isolator used in QC laboratory asepsis, microbial limit test. Aseptic test isolator is composed of test chamber, integrated bacteria collector, VHP sterilizer and necessary test port. Positive or negative pressure (used to protect the safety of drugs or operators) in the cabin. Sterile and microbial limit inspection, the sample (with packaging container), test equipment, culture medium and buffer incoming lab, pay attention to ensure that the sample (with packaging container), test equipment, fully exposed, such as medium and buffer can be through a dedicated sterilization, the optimum effect of sterilization, start the sterilization procedures VHP sterilization (sterilization) was carried out on the surface of microbes, after the sterilization, hold hydrogen peroxide residue after reaching safety levels, again through the gloves mouth inspection and microbial limit examination of aseptic operation. The laboratory chamber is equipped with a microbiometer for sterility test and microbial limit test. After the inspection, the isolator is sent through the external door.
