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35200PPC 0.5µ ISO Class 5 Cleanroom Pharmaceutical Turkey Project HEPA FFU

Guangzhou Anlai Airtech Co.,Ltd
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Address: Plant 106, No. 25, Taian Road, XINQIAO VILLAGE, PANYU DIST. GUANGZHOU CHINA

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Guangzhou Anlai Airtech Co.,Ltd

35200PPC 0.5µ ISO Class 5 Cleanroom Pharmaceutical Turkey Project HEPA FFU

Country/Region china
City & Province guangzhou
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Product Details

ISO Class 5 Cleanroom Design and Build

ISO 5 or Class 100 Cleanrooms are an ultra-clean stringent classification of cleanrooms across a narrower cross section of industries and application types. ISO 5 Cleanrooms are utilized in biotechnology, pharmaceutical, nanotechnology, and various cleantech manufacturing applications such as fine chemical, ion lithium battery, solar, active medical devices, and high-end film / packaging.
 
 
 

ISO 5 Cleanroom Design Specifications:

Specification
Model item
ISO 7 CLEAN ROOM
AL-CS4*6/C7
AL-CS5*10/C7
AL-CS6*12/C7
AL-CS7*20/C7
Size(mm)
4000*6000*2500
5000*10000*2500
6000*12000*2500
7000*20000*2500
Material
Framework
Cold rolled steel /Aluminum/Stainless steel/sandwich panel
Around
Plexiglass,Soft curtain,Anti-static strip curtain/sandwich panel
Clean Class Level
10000
10000
10000
10000
HEPA filter
Size(mm)
610*610*69
1220*610*69
1220*610*69
1220*610*69
Efficiency(%)
99.99
99.99

 

99.99
99.99
Air flow (m3/h)
3600
7500
10800
21000
Pre filter
Size(mm)
Optional
Motor Spec
Power supply
220V/50Hz
220V/50Hz
220V/50Hz
220V/50Hz
Noise(dB)
62
63
62
63
Filtration & Particle Control:
  • Focused measurement of particle sizes greater than 0.5µ and less than 5.0µ
  • High Efficiency Penetration Air (HEPA) Filtration efficiency: 99.99% at 0.3 microns
  • Final filtration is performed at the air entry point of the cleanroom, and is commonly performed by terminal HEPA modules or HEPA FFU (fan filter modules) depending on the application.
  • 35,200 PPC (particles per cubic meter) at 0.5µ
  • Environmental parameters such as temperature, humidity, lighting levels, noise criteria, static control, and outgassing are often driven by the requirements of the specific process being performed in the cleanroom.

 

 

 

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