Product features
Cleanroom Expert
We are a leading clean room manufacturer specialize in modular clean room with 25 years of experience. Have obtained more than 100 modular cleanroom patents,we become a clean room expert by strong design and production capabilities and years of in-depth research on customer production environment needs, to deliver customized solutions tailored to various cleanroom projects.
Our intelligent manufacturing facility is certified by ISO 9001 and TÜV, and ourcertified cleanrooms meet international standards such as UL, CE, and FCC. Our products have been widely adopted bywell-known enterprises, including Sony, Canon, TCL, BYD, PHILIPS, BGI, GE Healthcare, DuPont, and The United Laboratories.
Diverse Clean room Panel Options
The AK-Light Series Modular Cleanroom has bright and clear visualexperience. And we offers a variety of cleanroom panel material optionssuch as acrylic, PC, PP and Tempered glass.-Acrylic Cleanroom Panel: High transparency, excellent chemicalresistance, and easy cleaning.
- PC Cleanroom Panel: High strength, superior thermal insulation, and excellent light transmission.
- PP Cleanroom Panel: Strong chemical stability, lightweight, and moisture-resistant.
- Tempered Glass Cleanroom Panel: High transparency and strength, with a smooth surface for easy cleaning
Additionally, we offer cleanroom panels with anti-static and fire-resistantproperties to meet diverse clean room wall requirements for different modular clean room applications.
Why Choose Modular Cleanrooms
- Reducing 45% construction time
Installation is usually completed within 3 to 7 days. It’s easy to disassemble and upgrade, making it a highly flexible solution. - Modular Cleanroom Structure
Modular cleanroom is a quick-install modular structure, HVAC system, and intelligent control system to rapidly create a clean room environment free of dust and aseptic. - Lower Clean Room Cost
Compared to traditional cleanroom, modular clean room with lower clean room cost, while reducing energy consumption costs, saving labor costs. It’s a more cost-effective options.
Modular cleanroom HVAC system Intelligent Control Panel
- Variable speed control Lighting control
- Relying on advanced sensor network, it can 24/7 real-time monitor key parameters such as cleanroom temperature, cleanroom humidity, pressure difference, and airborne particle levels.
- If there is any abnormality, the system alarm will be promptly adjusted to ensure optimal clean room HVAC performance.
Modular Cleanroom Structure
- Super high, Large span
- FFU-900
- Double-sided laminated tempered glass
- Aluminum frame
- Diffuser
- Auto double sliding door
- Swing double door
- Intelligent control panel
- Fast Roll-up door
FFU with H14 HEPA filter ISO Class 4-9 optional
The FFU (fan filter unit) on the top of the modular cleanroom adopts a high-efficiency and low-noise design, which can easily create an ISO4-9 clean space. Including ISO5, ISO7, and ISO8 cleanrooms. The FFU clean room system supports centralized group control functions,can uniformly control multiple groups of FFU through an intelligent control system, flexibly adjust the air velocity and air volume, ensure uniform and stable indoor airflow, effectively avoid airflow dead corners.Also optimizes cleanroom pressure control. Greatly improve the overall performance and operating efficiency of the clean room.
Single/double door
Modular clean room doors provide a variety of options such as hinged doors, cleanroom
sliding doors, emergency escape doors, etc.to meet different application needs.
The doors can be equipped with an interlocking system and access control locks. Standard
cleanroom doors equipped with electronic interlock system,
Ensuring safe and orderly personnel movement while preventing cross-contamination in the clean area.
cleanroom doors equipped with electronic interlock system,
Vent diffuser
The vents are equipped with diffusers to automatically balance the air pressure, ensuring uniform and stable cleanroom air flow. Creating a good air environment for the clean room and preventing air pressure and airflow problems from affecting production experiments.
Modular Clean Room Design
- Modular design Lower costs and flexible structures
- Prefabricated and assembled before delivery, fast installation
Turnkey cleanroom solutions trial operation and test before delivery Ensure quality and performance
Including clean class test to ensure cleanroom maintain designed ISO class We provide turnkey cleanroom solutions, including modular clean rooms, that comply with GMP cleanroom and cGMP cleanroom standards, as well as USP 797 and USP 800 cleanroom requirements. Our expertise ensures clients achieve high-efficiency, fully compliant cleanroom environments.
Turnkey modular cleanroom solution Big or small, all fully equipped
- Fast installation, plug-and-run mechanism Air shower, pass box, laminar flow hoods optional freely
Diverse layout
- whatever size and shape, customizable
HVAC system optional to control T, RH and DP
Clear acrylic wall for high clarity
- Non-transparent acrylic for privacy Different types of walls can be integrated together
Li-ion Batteries Modular Cleanroom
- Lithium battery production requires strict control of temperature, humidity, and air cleanliness to ensure product safety, consistency, and service life.
- AIRKEY-LIGHT modular cleanrooms support ISO 5 or higher environments and ultra-low dew-point control down to −45°C, making them suitable for coating, slitting, and other critical processes.
- With stable performance, fast installation, and flexible expansion, they help battery manufacturers increase production capacity efficiently.
ISO Cleanroom Classification
- A cleanroom is a controlled environment where airborne particle concentrations are strictly regulated. ISO cleanroom levels range from ISO 1 to ISO 9, with lower numbers representing higher cleanliness.
- ISO 1–3 are used for extremely sensitive environments, while ISO 4–6 are commonly applied in electronics, pharmaceutical, and precision manufacturing. ISO 7–9 are suitable for general controlled production areas with lower cleanliness requirements.
GMP Cleanroom Classification
- GMP cleanrooms are classified into Grades A, B, C, and D according to airborne particle and microbial limits under at-rest and operational conditions.
- Grade A provides the highest level of protection for critical operations, Grade B supports adjacent aseptic areas, while Grades C and D are used for less critical production and preparation processes. Each grade has specific limits for particles and microbial contamination.
Specification
| Clean class | ISO 4-8 Confirm or recommend as per request or production process |
| Structure | Closed/leveling cup/wheels |
| Power | 1P/220V/50Hz 1P/110V/60Hz |
| Size | Customize based on customers’ demands No size, height, or span limitations |
| Control panel | Basic Type: air speed control/LED light control/ pressure display Intelligent type: T/RH/pressure control, filter alarm, speed regulation |
| Frame | SS304/Aluminum Alloy |
| Walls | Transparent acrylic glass ESD acrylic/non-transparent acrylic glass, or tempered glass optional |
| Ceiling | Ceiling panels |
| FFU | Size: 1175*575*300mm HEPA filter: H14,99.995%@0.3μm Qty: determined according to clean class and dimension of cleanroom |
| Cleanroom equipment | Air shower/cargo air shower/pass through/Buffer Room/Clean Wardrobe/Cleanroom Furniture optional to be equipped |
| HVAC | HVAC optional: temperature control only/ temperature and humidity control |
Product video
Gallery
Modular cleanroom for pharmaceutical 1
Modular cleanroom for semi-conductor 1
Modular cleanroom for electronics 1
Modular cleanroom for pharmaceutical 2
Modular cleanroom for labs 1
Modular cleanroom for cell incubation labs 1
Modular cleanroom for pharmaceutical 3
Modular cleanroom for lithium battery 1
Modular cleanroom for electronics 2
Modular cleanroom for pharmaceutical 4
Modular cleanroom for cell incubation labs 2
Modular cleanroom for pharmaceutical 5
Modular cleanroom for medical 1
Modular cleanroom for medical 2
Modular cleanroom door for electronics 3
Modular Cleanroom Application
AIRKEY modular cleanrooms are designed to meet the strict environmental requirements of various industries.
3-7 days fast installation, flexible expansion, and reliable contamination control.
Our cleanroom can be customized to create precise cleanliness levels for semiconductor cleanroom,
electronics cleanroom,pharmacy clean rooms,operating rooms,hospital operating theaters,veterinary laboratories,
food processing &packaging clean rooms andbiotechnology laboratory.
Pharmaceutical Manutacturing
Medical Operating Room
Electronics Industry
Semiconductor Industry
Biotech Lab Cleanroom
Renewable Energy Industry
Recent Projects
ISO 5 Modular Cleanroom Manufacturer for Medical Research in Singapore
ISO 7 Modular Cleanroom Manufacturer for Pharmaceutical Packaging in the USA
ISO 6 Modular Cleanroom Manufacturer for Optical Component Production in Germany
GMP-Compliant Laminar Airflow Hood for Pharmaceutical Manufacturing in Australia
ISO 6 Modular Cleanroom Manufacturer for Cell Technology Research in Oman
ISO 5 Modular Cleanroom Solution for Peptide Production in the USA
Frequently Asked Questions
1. What is a modular cleanroom?
Modular cleanrooms, also known as assembled cleanrooms, are a kind of partial purification equipment specially designed to control the level of air pollution removing pollutants such as micro-particles, harmful gas, bacteria and controlling the indoor temperature and humidity, cleanliness, differential pressure, air velocity, airflow distribution, noise vibration and lighting, and static electricity within a certain required range,and ensure high-precision work or product experiments and manufacturing, which can quickly improve the clean class of the area.
2. What is the cost of modular cleanroom?
The cost of modular clean rooms depends on many factors, including ISO classification requirements, area, height, material selection, special needs, and supporting facilities. According to the different needs of customers, corresponding modular clean room solutions and cost budgets can be designed. The main installation components of modular clean rooms are prefabricated in Airkey factory, to realize quick and easy installation on site, which can greatly shorten the construction period and reduce the labor cost of on-site construction. Therefore, the overall cost of modular clean rooms is about 20% lower than that of traditional clean rooms, and the installation period can be saved by 40~50%.
3. What are the benefits of modular clean rooms over traditional cleanroom?
Compared with traditional clean rooms, modular clean rooms have the following advantages:
- Quick installation: Modular clean rooms use prefabricated modules, which are easy and quick to install, greatly shorten the construction period
- Flexible layout: The modular cleanroom design can be customized according to your needs, and the floor plan is more flexible and changeable to meet the ever-changing work needs.
- Slight impact on the on-site environment: Modular clean rooms are only assembled on site, without material cutting and processing, reduces pollution and noise, can maintain a clean working environment.
- Energy saving and environmental protection: Modular clean rooms use advanced energy-saving technologies to effectively reduce energy consumption. At the same time.
- Simple maintenance: Simple daily cleaning & maintenance, providing convenience for your daily operations.
- High cost-efficiency: Modular clean rooms are less expensive and have a shorter installation cycle than traditional clean rooms, therefore, more cost-effective.
- Mobility and scalability: The design of modular cleanrooms takes into account mobility and adjustability. It can be quickly rearranged or expanded according to process requirements, or disassembled and relocated to improve production efficiency and flexibility.
4.How modular cleanrooms are applied?
Modular cleanrooms are designed to quickly provide a local clean and controlled environment that meets process requirements. They can be widely used in food processing, electronics, scientific experiments, pharmaceuticals and other fields. In the field of food processing, modular clean rooms can be used as dust-free food workshops to ensure the cleanliness of the food production environment and improve food safety standards; in the field of electronics, dust can cause short circuits in electronic devices and affect performance. Modular clean rooms can create a designated production environment with minimum and controlled particles ; in the pharmaceutical field, modular clean rooms can provide a highly clean production environment to ensure the quality and safety of drugs; in the laboratory field, modular clean rooms provide research spaces that meet specific environmental requirements to ensure the accuracy and reliability of experimental results. In the future, with the accelerated development of downstream industries, modular clean rooms will have an expanded and bigger market.
5. What information does the customer need to provide for clean room design?
The information required for clean room design includes: thepurpose of clean room, thefloor plan and size of clean room, and the configuration requirements of production equipment (the number of production equipment and water and electrical parameters are crucial to the design and calculation of clean room air purification system, HVAC and pressure control system); Industry standards (If the design of the clean room is required to comply with a specific industry standard or specification, the customer should provide relevant information such as GMP,FDA, etc., to ensure that the design meets the relevant regulatory requirements). In addition, if the customer has other specialrequirements, such as energy saving requirements, safety considerations, etc., these special requirements need to be fully considered and realized in the design stage.
6.What modifications are required for enclosed cleanroom applications?
The modifications toenclosed cleanroom applications mainly include comprehensive evaluation of the cleanroom structure, purification and air conditioning equipment, and indoor environment, and corresponding modifications and optimization. First of all, a comprehensive inspection of all equipment in the cleanroom is required to ensure that the equipment can operate normally; at the same time, various parameters of the clean area are tested (including cleanliness, temperature and humidity,air velocity, etc.) to determine whether the indoor environment meets the standards. Combined with the equipment status and indoor parameters, determine whether there is a need for modification and the scope of modification. The transformation mainly considers the requirements of process equipment and environmental conditions. By reasonably transforming the existing air purification system, the indoor air quality can reach the predetermined cleanliness standard, reduce the indoor dust concentration, and timely discharge the pollution generated indoors, so as to improve the application effect of the closed clean room and ensure the quality and reliability of the product.
7.What are the levels of clean rooms?
Clean rooms are divided into different grades according to the maximum allowable concentration of suspended particles of different particle sizes in thecleanroom air, and nine different levels of clean rooms such as cleanliness level 1-9 are specified in the ISO.
In addition, the grade standard of GMP ondrug production clean room is divided into four grades: A, B, C and D, and each grade is also divided according to the maximum allowable concentration of suspended particles of different sizes in the indoor air under different states.