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portugal clean class 10000 modular cleanroom done by anlaitech in 2024-0

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Portugal Clean Class 10000 Modular Cleanroom Done by anlaitech in 2024

Analitech is hornored to be part of Medical device clean room project for our Portugal customers. From 2009, anlaitech is concentrated in clean room R&D, produce, servivce and exporting for overseas customers, customers compared serveral companys...

Portugal Clean Class 10000 Modular Cleanroom Done by anlaitech in 2024

Analitech is hornored to be part of Medical device clean room project for our Portugal customers.

From 2009, anlaitech is concentrated in clean room R&D, produce, servivce and exporting for overseas customers, customers compared serveral companys, verified anlaitech is the trustworthy partner for their project.

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What's the key to ensure air quality?

The Cleanroom Airflow Management absolutely it is very important one, Cleanrooms are carefully designed, dedicated spaces with extremely low concentrations of airborne particles.

Manu facturers of pharmaceuticals, electronic components, and other high-value, high-demand products produce and process them in cleanrooms to prevent contaminants from interfering with product performance.Airflow management plays a vital role in maintaining the efficient operation of cleanrooms, ensuring that air flows properly and cleanly, thereby protecting the integrity and reliability of the products.

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How Industry conditions determine cleanroom airflow requirements?

Those involved in maintaining proper cleanroom air flow must also understand industry details that may affect their work. For example under the previous federal standard 209E framework, there were three fewer cleanroom classes. However, the United States and Canada now follow the requirements of lSO 14644-1.lt expresses the decimal logarithm of particles 0.1 microns or larger per cubic meter of air. However, some cleanroom classes have additional details.

In a class 7 cleanroom, the concentration of particles 0.5 microns or larger must be less than 352,000, and the number of particles 1-4microns

must not exceed 83,200. The number of particles 5 microns and above must be less than 2930.

Familiarity with specific industry standards and regulatory requirements is the best way to prioritize safety and prevent product recalls fines, or other adverse consequences due to poor airflow management.

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ISO 5 CLEAN CLASS AREA

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ISO7 packing area

We are continusely servicing with this project for running.

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