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AM-PB23
Amber
AM-PB23
The Clean Room Wall Pass Through is an enclosed passageway installed on the wall of a clean room, designed for the transfer of goods between areas of different cleanliness levels. By avoiding the frequent entry and exit of personnel, it effectively reduces the risk of cross contamination in the cleanroom. Commonly used in pharmaceutical, biological, electronic manufacturing and chemical laboratories, it is an important part of the Pass Box Laboratory configuration.
The Clean Room Wall Pass Through is designed to be clean, corrosion resistant and easy to maintain. As a result, this Pass Box has excellent chemical resistance and is suitable for use in environments containing corrosive chemicals or disinfectants, extending the life of the equipment.
The Pass Through Box is also equipped with a double door interlock system to ensure that only one side of the door is open, preventing cross contamination of airflow. UV sterilising lamps, electronic interlocks and air shower systems are also available as options.
Most importantly, This Pass Through Box can be mounted on the clean room wall, saving space while ensuring safe transport of materials.
If you want to know more details about the parameters of Clean Room Wall Pass Through, you can consult our Amber Team by Email or online.
Q1: Can Clean Room Wall Pass Through be customised in terms of size and material?
A: We offer a wide range of customised sizes, door opening methods and materials, including 304/316 stainless steel, anti-corrosion, etc., to meet the needs of customers with different cleanroom wall structures and usage requirements.
Q2: What is the difference between Pass Box and ordinary Pass Box?
A: Clean Room Wall Pass Through adopts embedded wall installation, with better structural sealing and cleanliness management, which is especially suitable for high-standard pharmaceuticals, laboratories and semiconductor workshops. The ordinary Pass Box is mostly independent floor-standing type, which is limited in applicable places and cleanliness level.
The Clean Room Wall Pass Through is an enclosed passageway installed on the wall of a clean room, designed for the transfer of goods between areas of different cleanliness levels. By avoiding the frequent entry and exit of personnel, it effectively reduces the risk of cross contamination in the cleanroom. Commonly used in pharmaceutical, biological, electronic manufacturing and chemical laboratories, it is an important part of the Pass Box Laboratory configuration.
The Clean Room Wall Pass Through is designed to be clean, corrosion resistant and easy to maintain. As a result, this Pass Box has excellent chemical resistance and is suitable for use in environments containing corrosive chemicals or disinfectants, extending the life of the equipment.
The Pass Through Box is also equipped with a double door interlock system to ensure that only one side of the door is open, preventing cross contamination of airflow. UV sterilising lamps, electronic interlocks and air shower systems are also available as options.
Most importantly, This Pass Through Box can be mounted on the clean room wall, saving space while ensuring safe transport of materials.
If you want to know more details about the parameters of Clean Room Wall Pass Through, you can consult our Amber Team by Email or online.
Q1: Can Clean Room Wall Pass Through be customised in terms of size and material?
A: We offer a wide range of customised sizes, door opening methods and materials, including 304/316 stainless steel, anti-corrosion, etc., to meet the needs of customers with different cleanroom wall structures and usage requirements.
Q2: What is the difference between Pass Box and ordinary Pass Box?
A: Clean Room Wall Pass Through adopts embedded wall installation, with better structural sealing and cleanliness management, which is especially suitable for high-standard pharmaceuticals, laboratories and semiconductor workshops. The ordinary Pass Box is mostly independent floor-standing type, which is limited in applicable places and cleanliness level.
