Marya Advanced Modular Cleanroom System Design for Pharmaceutical Manufacturing

Customization: Available
Application: Petrochemical Industry, Precision Electronic Industry, Pharmaceutical,Food Industry, Auto Industry
Certification: CE, ISO, RoHS

Product Description

Basic Info.
Model NO.
AA
Fuel
Electric
Structure
Bilateral Air Shower
Feature
Fast Shutter Door, Automatic Door
Number of Nozzles
6
Applicable Object
People Shower
Material
Stainless Steel
Machine Power
380V 50Hz
Mist Particle Size
10~50um
Nozzle Wind Speed
≥20m/S
Origin
China
Production Capacity
5000pieces/Year
Product Description
Advanced Modular Cleanroom System Design for Pharmaceutical Manufacturing

This advanced modular cleanroom system delivers precision-controlled environments for pharmaceutical production, ensuring compliance with ISO 14644 and GMP standards. Featuring customizable layouts, HEPA/ULPA filtration, and seamless HVAC integration, our cleanrooms minimize contamination risks while optimizing energy efficiency. The modular design allows rapid deployment and scalability, adapting to facility expansions or process changes. With real-time monitoring (temperature, humidity, particle count) and durable, antimicrobial surfaces, this solution guarantees sterility for critical applications like sterile filling and vaccine production. Ideal for upgrading existing facilities or new builds, our turnkey systems reduce downtime and long-term operational costs. Trust this cutting-edge cleanroom technology tailored to pharmaceutical excellence.

Modular Cleanroom System Design Pharmaceutical Manufacturing Cleanroom
Key Features
  • Modular design with a compact structure for efficient space utilization.
  • Constructed entirely from high-grade full stainless steel SUS304.
  • Photoelectric control for automated blowing and showering operations.
  • Ventilation circulation design utilizing HEPA filtered air to maintain cleanliness in the mist area.
  • Equipped with an airtight sealing box and electromagnetic interlock doors for maximum safety.
  • Programmable PLC control system allowing for customized settings of time, period, and spray duration.
  • Optional anti-static device integration available.
Product Parameters
Specification Item Technical Data
Filtration Efficiency≥99.99% @ 0.5μm (sodium flame method)
Air Shower Time (s)1~99 seconds adjustable (default 20s)
Mist Shower Time (s)1~99 seconds adjustable (default 20s)
Mist Particle Size10~50 μm
Spray Nozzle Air Speed≥20m/s
Mist Shower Nozzle Number6
Air Shower Nozzle Number6
Overall Dimensions1150W * 1000D * 2100H
Air Shower Area800W * 900D * 1950H
Power Consumption3N 380V 50Hz (Max 1KW)
HEPA Filter Size610*610*70 (1pc)
About & Workshop
About System
Production Workshop
Certification & Projects
Certificates
Project Case
Customer & Exhibition
Our Customer
Exhibition and Team
Packaging & Shipping
Packaging and Shipping
Frequently Asked Questions
What standards does the modular cleanroom system comply with?
The system is designed to meet international ISO 14644 and GMP standards, ensuring high-level sterility and environmental control for pharmaceutical manufacturing.
What material is used for the construction of the air shower?
The entire structure, including doors and nozzles, is made from high-quality SUS304 stainless steel, which is antimicrobial and highly durable.
How does the air shower control system operate?
It utilizes a programmable PLC with photoelectric sensors. This allows for fully automatic blowing and showering with customizable cycle times via a user-friendly interface.
What is the filtration efficiency of the system?
The system achieves a filtration efficiency of ≥99.99% for particles as small as 0.5μm, verified by the sodium flame method.
Is the system energy efficient?
Yes, the integration of modular design with optimized HVAC and circulation systems ensures high performance while minimizing energy consumption.
Can the cleanroom layout be customized?
Absolutely. The modular design is specifically engineered for scalability and rapid deployment, allowing for customized layouts that adapt to specific facility needs or process changes.

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