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Biochemical GMP Clean Room Workshop ISO Modular Custoimzed Pharmaceutical Cleanroom1
Air Clean Equipment, Other Air Clean Equipments, ISO Modular Cleanroom, Class 10000 Clean Room
Suzhou Pharma Machinery Co., Ltd.
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Product Description ParameterSoftwall Clean BoothHardwall Clean BoothCleanlinessFrom Class 100 to Class 10,000External DimensionAs per requirementFFUDimension2'X4'Cabinet MaterialStainless SteelPower source110V/60hz/av/dc, 220V/60HZ/AV/DCHEPA FilterH14 Hepa filterFrame MaterialStainless SteelWall MaterialAnti-static soft PVC wall 106~109ΩAnti-static acrylic 106~109ΩLightingLampsAvailable in LED and T5Air conditionAs per requirementAvailable in constant temperature air conditioner/constant temperature and humidity conditionerApplicationFlexible assembly: Compared to the tradtitional clean booth it is easy to installation, cost effective with less investment andquick return, as it cost shorter construction period in the assembling frame by manufacturer.Selected high quality material: import for the grind curtain and adjustable plastiv cup and universal wheel, convenience forinstallation and maintance.Humanized structure: Compared to the clean bench it has the multi-function, which can be used as a unit or combined withanother clean equipment together. Even you can assemble it on the production line to change dust-free production.Flexibility: Less limitation or low requirements for the floor and spot situation, the iner space is enough to use and theframe canbe recycledIn a pharmaceutical production packaging cleanroom designated as ISO 8, rigorous controls are in place to minimizethe introduction and spread of contaminants, ensuring the integrity and safety of the packaged pharmaceutical products.This includes controlling air flow, using High-Efficiency Particulate Air (HEPA) filtration systems, maintaining strictgowning procedures, limiting access, and regularly monitoring and testing the environment for particle counts andmicrobiological contaminants. Despite being less stringent than some other cleanroom classifications, an ISO 8 cleanroomstill plays a vital role in preventing contamination that could compromise the efficacy or shelf life of pharmaceuticals.
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