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Shenzhen Meiri Purification Technology Co., Ltd.

  • China,Shenzhen ,Guangdong
  • Verified Supplier
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China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology
China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology

  1. China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology
  2. China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology
  3. China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology
  4. China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology
  5. China Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology

Pharma-Grade ISO 5 Certified Laminar Flow Cabinet with Liquid Seal Technology

  1. MOQ: 1
  2. Price: Contact Us
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custom made support
Delivery Time 7-15 working days
Brand Name MRJH
Model Number Laminar flow hood
Certification ISO 14644,CE,GMP,FDA,UL
Place of Origin Guangdong, China

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  1. Product Details
  2. Company Details

Product Specification

custom made support Delivery Time 7-15 working days
Brand Name MRJH Model Number Laminar flow hood
Certification ISO 14644,CE,GMP,FDA,UL Place of Origin Guangdong, China
Pharma-Grade Liquid Seal Laminar Flow Cabinet | ISO 5 Certified Filtration
Aseptic processing laminar flow cabinet featuring patented liquid-trough sealing technology and H14 HEPA filtration. Validated for ISO 14644 Class 5 compliance.
Parameter Name Value
Main Body Material Stainless steel 304# sandblasted plate, 1.0mm thickness
HEPA Filter Specifications 1100+500×93mm
Fan Configuration Aluminum alloy impeller low-noise fan, 200W 50Hz
Pressure Differential Monitor Digital gauge 0-500Pa (±1% accuracy)
Detection Port Integrated DOP test kit port
UV Sterilization Optional 36W germicidal UV-C lamp (254nm wavelength)
Air Velocity 0.45-0.75 m/s adjustable
Noise Level ≤60 dB(A) at 1m distance
Control Interface Touchscreen display with real-time monitoring
Product Features
  • Absolute Containment Technology - Continuous ethanol liquid trough creates hermetic seal (no gasket degradation). Maintains ISO 5 conditions during dynamic operations.
  • Regulatory-Compliant Design - Pre-validated per EU GMP Annex 1 & FDA 21 CFR 210/211. Integrated DOP test ports for filter integrity verification.
  • Smart Monitoring System - Real-time differential pressure tracking (0-500Pa). Touchscreen with alarm thresholds for critical parameters.
  • Decontamination Ready - 316L stainless steel withstands VHP/SIP cycles. Optional UV-C system (40mJ/cm² dose).
  • Ergonomic Operation - 55dB noise level for communication clarity. Glove-compatible control interface.

Application Scenarios
  • Sterile Injectable Manufacturing - Maintains Grade A zone during vial filling/stoppering. Prevents microbial ingress in lyophilizer loading.
  • ATMP Production - Protects cell therapies during media transfers. ESD-safe materials for sensitive biologics.
  • Vaccine Fill-Finish - Validated for live virus workflows. Withstands formaldehyde fogging decon.
  • Implantable Device Packaging - Particle-free environment for Class III devices. Compatible with cleanroom robotics.

Technical Validation
  • Filter Efficiency Testing - Certified via EN 1822-5:2009 MPPS method. PAO/DOP challenge testing available upon request.
  • Material Compliance - 304 stainless steel meets ASTM A240/A480 standards. UV-C lamp output verified per FDA 21 CFR 1040.20.
  • Operational Safety - Emergency stop function triggers immediate airflow reversal. Interlocked UV system deactivates upon door access.
Pharma-grade laminar flow cabinet interior view showing liquid seal technology Close-up of HEPA filtration system and control interface Laminar flow cabinet in cleanroom manufacturing environment Technical validation and testing setup for ISO 5 certification
Frequently Asked Questions
How does liquid sealing outperform traditional gaskets in sterile processing?
The ethanol barrier eliminates compression fatigue and microbial harborage points, providing consistent containment through 10,000+ cycles (validated per ISO 14644-3).
What documentation supports regulatory submissions?
Includes IQ/OQ templates, material certifications (USP Class VI), and filter test reports per IEST-RP-CC034.3.
Can the system accommodate large component transfers?
Customizable work zones up to 1200mm width maintain ≤0.5% velocity deviation across entire surface.

Company Details

Bronze Gleitlager

,

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 and 

Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter

  • Year Established:

    2012

  • Total Annual:

    1500000-2000000

  • Employee Number:

    100~200

  • Ecer Certification:

    Verified Supplier

Shenzhen Meiri Purification Technology Co. Ltd., known by our brand "MRJH," is a leading manufacturer of cleanroom equipment based in Shenzhen, China. With a spacious facility spanning over 30,000 square meters, we specialize in the research, development, production, sales, and service of profession... Shenzhen Meiri Purification Technology Co. Ltd., known by our brand "MRJH," is a leading manufacturer of cleanroom equipment based in Shenzhen, China. With a spacious facility spanning over 30,000 square meters, we specialize in the research, development, production, sales, and service of profession...

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Get in touch with us

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  • Shenzhen Meiri Purification Technology Co., Ltd.
  • No. 79, Langbei Village Industry Road , Tongde Community , Baolong Street , Longgang District, Shenzhen City , Guangdong Province , China
  • https://www.ffu-cleanroom.com/

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