Shenzhen Meiri Purification Technology Co., Ltd.

MAKE ROOM JUST HYGIENIC

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Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

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Shenzhen Meiri Purification Technology Co., Ltd.
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City:shenzhen
Province/State:guangdong
Country/Region:china
Contact Person:MrNeal Liao
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Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

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Brand Name :MRJH
Model Number :Class 100 clean room 2800
Certification :ISO 9001、CE、ISO 14644
Place of Origin :Guangdong, China
MOQ :1
Price :Detailed communication
Delivery Time :7-15 days
size :W15000 × D16000 × H2700 (mm)
custom made :support
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Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

The Clean Booth is designed to maintain ISO Class 5 (Class 100) air quality for contamination-sensitive processes, compliant with ISO 14644-1 standards. Constructed with 304 stainless steel square tubes and transparent mesh curtains, it is ideal for large-scale industrial applications, including electronics, pharmaceuticals, and biotechnology. Equipped with 34 HEPA FFUs, 72 flat panel lights, and dual curtain doors, it ensures robust airflow control, uniform illumination, and contamination-free operations.

Parameter Name

Value

Material

304 stainless steel frame with transparent mesh curtains

Internal Design

72× flat panel lights (1200×300 mm), 2× curtain doors (1500×2100 mm)

Filtration System

34× FFU (1175×575×285 aluminum frame HEPA filters, 1170×570×69)

Control System

Distribution box for power management

Airflow & Noise

Noise: 48–58 dB ±5dB; Rated power: 150–190W ±5W per unit; Vibration: ≤5µm

Fan & Filtration

HEPA filtration efficiency ≥99.995% @ 0.3µm

Lighting

Integrated clean lighting

External Dimensions

W15000 × D16000 × H2700 (mm)

Certifications

ISO 9001

Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

Key Features

1. Stainless Steel Durability: 304 stainless steel frame with corrosion resistance for industrial-grade reliability.

2. High-Capacity Filtration: 34× FFUs with non-partitioned HEPA filters (99.995% @ 0.3µm) ensure ISO Class 5 compliance.

3. Industrial Lighting: 72× flat panel lights (1200×300 mm) for full-area illumination in large clean environments.

4. Low-Noise Operation: Optimized FFUs with ≤5µm vibration and noise levels of 48–58 dB.

5. High-Power Efficiency: 220V/50Hz power supply with 150–190W ±5W per FFU for scalable energy management.

6. Large-Scale Design: Spacious dimensions (15000×16000×2700 mm) and dual curtain doors for heavy-duty workflows.


Application Scenarios

Electronics Manufacturing: Contamination-free assembly of sensitive components.

Pharmaceutical Cleanrooms: Material handling and processing in ISO Class 5 environments.

Biotechnology Labs: Sterile sample preparation and testing.

Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

Tailored Cleanroom Enclosures | HEPA Filtration Systems | Made-to-Order ISO Compliance

FAQ 1: How do your tailored cleanroom enclosures adapt to unique facility layouts without costly modifications?
A: Our tailored enclosures use modular components and precision-engineered panels, ensuring seamless integration into existing spaces. Custom sizing and HEPA placement eliminate structural changes, while maintaining ISO-compliant airflow for your specific workflow.
FAQ 2: What guarantees the long-term efficiency of HEPA filtration systems in high-demand environments?
A: Equipped with H13/H14 HEPA filters and real-time pressure sensors, our systems auto-alert for filter changes (typically 18-24 months). Redundant sealing and ISO 14644-3 testing ensure particle capture >99.995% even in 24/7 operations.
FAQ 3: Does "made-to-order ISO compliance" cover industry-specific regulations like pharmaceutical GMP or semiconductor protocols?
A: Absolutely. Each enclosure is certified to ISO 14644 Class 5-8, with optional add-ons (anti-vibration mounts, humidity control) to meet FDA 21 CFR Part 11, EU GMP Annex 1, or SEMI S2 standards.

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