Double doors of clean room
As you know, clean room doors are one of the most vital parts of a clean room. To control particles suspended in the air, we offer single-leaf and double-leaf doors equipped with an interlock system. This product is produced and equipped in compliance with all international standards, including ISO 1 to 8, which is introduced and translated in the following article by Barsam Padideh Raimon, which designs and implements a safe and secure environment.
General review of clean room doors
It should be noted that when choosing clean room doors, you should consider several things, including product material, sealing, hinges, locks, and windows, that the accurate selection of clean room door specifications and accessories will help ensure that you Ensure your clean room is free of contaminants and built according to clean room standards. Clean room doors are adjustable and custom sizes are available, enabling customers to specify desired size and Receive your product according to the desired standards.
Consulting, design and implementation
Barsam Padideh Raimon Company, abbreviated as Raimon Group, is an international company in the fields of conceptual design, foundation and details, design of production lines and machinery, scheduling, project management and control, import and export, testing and validation and documentation of processes, as well as consulting for obtaining Domestic and international production licenses in the pharmaceutical and related industries. Raymon Group is the exclusive representative of R.K ENGINEERING in Iran, which has successful projects in the fields of medicine, biotechnology, medical equipment, cosmetic and health industries, medicinal plants, livestock products and related products of these industries all over the world. Raymon Group has started its activity since 2017 and 2017 with the investment of domestic and foreign financial groups with the motto of fighting all kinds of diseases and has brought hundreds of domestic and international companies to the operational level.
ISO standards
1.The ISO 1 specification for cleanrooms requires less than 2 particles larger than 0.3 microns and no particles greater than 1.0 microns per cubic meter. An ISO 1 cleanroom typically has between 500-750 air changes per hour and typically uses ULPA filtration. Other common features are 100% ULPA roof covering and raised floors.
2.The ISO 2 specification for cleanrooms requires fewer than 11 particles larger than 0.3 microns and no particles greater than 1.0 microns per cubic meter. An IS0 2 cleanroom typically has 500-750 air changes per hour and typically uses ULPA filtration. Other common features are 100% ULPA roof covering and raised floors.
3.The ISO 3 specification for clean rooms requires no fewer than 102 particles larger than 0.3 microns and no more than 8 particles larger than 1.0 microns per cubic meter. An IS0 3 cleanroom typically has 500-750 air changes per hour and typically uses ULPA filtration. Other common features are 100% ULPA roof covering and raised floors.
4.The ISO 4 specification for clean rooms requires no fewer than 1,020 particles larger than 0.3 microns and no more than 2 particles larger than 5.0 microns per cubic meter. An IS0 4 cleanroom typically has 500-600 air changes per hour and typically uses ULPA filtration. Other common features are 100% ULPA roof covering and raised floors.
5.The ISO 5 specification is an ultra clean clean room classification. A clean room should have less than 3520 particles > 0.5 microns per cubic meter and 250-300 HEPA filtered air changes per hour. FED standard is equivalent to class 100 or 100 particles per cubic foot. Common applications are semiconductor manufacturing and pharmaceutical filling chambers.
6.The ISO 6 specification is a very clean clean room classification. A clean room should have less than 35,200 particles > 0.5 microns per cubic meter and 180 HEPA filtered air changes per hour.
7.The ISO 7 specification is a typical clean room classification. A clean room should have less than 352,000 particles > 0.5 microns per cubic meter and have 60 HEPA filtered air changes per hour. The FED standard is equivalent to a class of 10,000 or 10,000 particles per cubic foot. Common applications include USP800 pharmacy compounding rooms, electronics manufacturing, and medical device manufacturing.
8.ISO 8 specification is the least clean room classification. A clean room should have less than 3,520,000 particles > 0.5 microns per cubic meter and 20 HEPA filtered air changes per hour. In comparison, a normal office space is 5-10 times dirtier. The FED standard is equivalent to a class of 100,000 or 100,000 particles per cubic foot. Common applications include plastic extrusion for medical devices, e-liquid production, and food packaging.
Frequently Asked Questions
1. What is a clean room?
A clean room is a room with a filter to remove particles and pollutants suspended in the air. Clean rooms are used for production in places where a high level of cleanliness and sterility is required.
2. How clean are the cleanrooms?
They are clean enough that the standard class 100 has 100 particles per cubic foot. Compared to a typical office space, there are 500,000 to 1,000,000 particles per cubic foot.
3. Who needs a clean room?
Industries such as pharmaceuticals, compound factories and medical equipment are required to comply with health protocols that must use a sterile environment and clean room.
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