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Zhongsilifu (Tianjin) Biotechnology Co., Ltd
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Aseptic isolator

NegotiableUpdate on 01/12
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Overview
After the sterile isolator kills the initial contaminated bacteria in the cabin, the cabin maintains a positive pressure to maintain the sterile state inside, creating an A environment for conducting sterile inspection experiments.
Product Details

Aseptic isolatorIntegrated vaporized hydrogen peroxide sterilizer(VHP)After killing the initial contaminating bacteria inside the cabin, the cabin maintains a positive pressure to maintain a sterile state inside, creating aAEnvironment, sterile testing experiments can be conducted.

Performance Characteristics

1Intelligent control system with automatic operation, manual operation mode, expanded ports, and management program, powerful functions

2The parameters such as temperature, relative humidity, pressure, and hydrogen peroxide gas concentration inside the cabin (with optional concentration probes) can be monitored in real time, and support functions such as real-time printing and storage

3It has all the functions of sterile testing isolators currently available internationally,USP/EP/CHPRegulatory requirements

4The sterilization system adopts the advanced Vico two fluid conduit dosing technology in China, which can effectively ensure the stability and service life of equipment operation

5Optional industrial tablet computer, linear pump head bacterial collector, hydrogen peroxide concentration probe, handheld hydrogen peroxide concentration detector, video camera system, scanning system, data management system, online suspended particles, online floating bacteria, etc

Aseptic isolatorTechnical Specifications:

1Metal materials:304Stainless steel316Lstainless steel

2Non metallic materials: polyvinyl chloride, silicone

3Power supply:AC220V±22V

4Frequency:50Hz±1Hz

5Power:≤2500W

6Touch screen: Siemens touch screen/12Inch tablet computer

7Control: SiemensPLC

8Range of cabin pressure regulation:-80-80Pa

9Resolution with low humidity:0.1%

10Low temperature resolution:0.1℃

11Low pressure resolution:0.1Pa

12Requirements for purification level inside the cabin: staticA(Determined according to requirements)

13Leakage rate:≤0.5%vol/h

14Noise:≤75dB(A)

15Efficient filter:H14level

16Illumination:≥300LX

17Isolator airflow model: turbulent flow/laminar flow

18TheVHPSterilization cycle time: transfer window≤50Minutes, operation cabin≤2.5hour

Application field

1Suitable for sterile rooms, microbial limit testing rooms, or positive rooms in pharmaceutical companies.

2Suitable for sterile rooms, microbial limit testing rooms, or positive rooms in drug testing systems.

3Suitable for sterile rooms, microbial limit testing rooms, or positive rooms of medical device enterprises.

4Suitable for hospital preparation rooms.

5Suitable for microbiological testing of highly toxic and highly allergenic drugs.

6Suitable for microbiological testing of biological products, etc.

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