Gmp комнаты класса 100000 медицинская фармацевтическая чистая комната дизайн ОВКВ Iso 5
- Категория: Air Cleaning Equipment >>>
- Поставщик: Guangzhou,Airwoods,Environment,Technology,Co.,Ltd.
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Описание и отзывы
Трекер стоимости
| Месяц | Минимальная цена | Макс. стоимость |
|---|---|---|
| Sep-19-2025 | 12.55 $* | 13.48 $* |
| Aug-19-2025 | 12.16 $* | 13.42 $* |
| Jul-19-2025 | 10.61 $* | 11.74 $* |
| Jun-19-2025 | 12.7 $* | 13.2 $* |
| May-19-2025 | 10.95 $* | 11.87 $* |
| Apr-19-2025 | 11.5 $* | 12.85 $* |
| Mar-19-2025 | 11.81 $* | 12.16 $* |
| Feb-19-2025 | 11.93 $* | 12.69 $* |
| Jan-19-2025 | 11.69 $* | 12.23 $* |
Характеристики
Cleanroom Service
We are a turnkey solution manufacturer for different project in Domestic and Abroad.
* Site Survey
* HVAC System Consultancy
* HVAC System Design
* HVAC System Equipment and Materials Supply
* Site Installation and Commissioning
* Site Tranining
* Aftersales Support
Cleanroom Cases
Cleanroom Introduction
Cleanrooms are essential to any manufacturing process where particulate contamination can affect the quality of goods produced.
Specific clean room classifications and ISO class code descriptions provide protective guidelines and secure environments through controlled air filtration, which lowers the possibility of product contamination or large particulate interference within critical process manufacturing. Specific cleanroom requirements and ISO 14644-1 cleanroom standards are used to protect consumers from any potential flaw or mishandling of a product.
Additionally, clean room classifications require that positive pressure is continuously maintained while the cleanroom is operational. This process prevents contaminated air from flowing back within the clean air environment. This process allows clean filtered air to continuously flows from clean to less-clean spaces, allowing for continual air movement.
Specific clean room classifications and ISO class code descriptions provide protective guidelines and secure environments through controlled air filtration, which lowers the possibility of product contamination or large particulate interference within critical process manufacturing. Specific cleanroom requirements and ISO 14644-1 cleanroom standards are used to protect consumers from any potential flaw or mishandling of a product.
Additionally, clean room classifications require that positive pressure is continuously maintained while the cleanroom is operational. This process prevents contaminated air from flowing back within the clean air environment. This process allows clean filtered air to continuously flows from clean to less-clean spaces, allowing for continual air movement.
Specification
Airwoods Cleanroom turnkey project Service Scope:
Cleanroom Project Scope(from structure, HVAC,electric to autoc ontrol) | 1. Cleanroom Structure: Wall Panel, Ceiling Panel, Windows, Doors, Fttings, Flooring |
2. HVAC: AHU, Chiller, dehumidifier, Ducting, Piping, etc. | |
3. Electric: Lighting, Switch, Cables, Wires, Power Distribution Cabinet, etc | |
4. Auto- control: PLC Controller, Sensors for Humidity and Temperature, Control Panel | |
5. Process Piping System: Gas, Water Pipeline | |
Equipment | Air shower, Cargo shower, Mist shower, Dynamic pass box, Static pass box, Sampling booth,Weighing booth, Dispensing booth, Medicine stability test chamber, isolator, VHP sterilizer,Biological safety chamber, FFU, LAF, etc. |
Temperature | 21-27*C (or as per required) |
Humidity | 30-60°C (or as per required) |
Application | Pharmaceutical factory, hospital, medical device factory, electronics factory, food factory,cosmetics factory, etc. |
Qualification Documents | CE GMP ISO |
Full Service | FAT and SAT Service, Professional Consultation, Training, 24 hours technical support |
Cleanroom Equipment
Company Profile
