KeLing Purification Technology Company

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Filtration Grade cleanroom Hepa Filter using Hot Melt Glue for maximum performance

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Province/State:guangdong
Country/Region:china
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Filtration Grade cleanroom Hepa Filter using Hot Melt Glue for maximum performance

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Brand Name :KELING
Model Number :KEL-HF
Place of Origin :China
Certification :CE
MOQ :1
Price :Negotiation
Packaging Details :plywood packing
Delivery Time :10 working day
Payment Terms :T/T
Supply Ability :3000
Name :Cleanroom HEPA Filter
other name :Cleanroom Termial Filter
media :Glass Fibre Media
Gasket :EVA /PU
Seal :AB Glue
Pleats Type :Mini-Pleats
Filtration Grade :Hepa Filter
Filter Efficiency :99.995%@0.3um
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Product Description:

Particle Capture Efficiency & Certification Standards

Terminal HEPA filters must achieve ≥99.97% efficiency at 0.3μm particles (per EN 1822-1), while ULPA filters target ≥99.999% at 0.12μm (MPPS method). Key certifications include:

  • ISO 29463 (global standard for filter classification)
  • IEST RP-CC034 (testing procedures for cleanroom filters)
  • FDA 21 CFR 210/211 (pharmaceutical manufacturing compliance)
    Example: Semiconductor fabs require ULPA filters with ISO 35H-40H ratings to control sub-0.1μm photoresist contaminants. Testing involves DOP/PAO aerosol challenges and laser particle counters to validate efficiency across 0.1–0.3μm ranges.

Features:

  • Product Name: HEPA Air Filter
  • Name: Cleanroom HEPA Filter
  • Filter Efficiency: 99.995%@0.3um
  • Other Name: Cleanroom Termial Filter
  • Frame: Aluminum
  • Seal: AB Glue
Filtration Grade cleanroom Hepa Filter  using Hot Melt Glue for maximum performance

Technical Parameters:

Seal AB Glue
Filtration Grade Hepa Filter
Name Cleanroom HEPA Filter
Application Cleanroom Termial Filteration System
Media Glass Fibre Media
Other Name Cleanroom Termial Filter
Spacer Hot Melt Glue
Frame Aluminum
Filter Efficiency 99.995%@0.3um
Gasket EVA /PU

Applications:

Pharmaceutical Manufacturing

Terminal HEPA filters (≥99.97% efficiency at 0.3µm) are mandatory in aseptic processing areas for injectables, vaccines, and biologics. They maintain ISO 5 (Class 100) environments in fill-finish lines, preventing microbial and particle contamination. Filters with DOP ports 2 enable integrity testing per FDA/EU GMP guidelines. Critical zones use laminar airflow units with ULPA filters (99.999% efficiency) to protect sterility during vial filling. HVAC systems integrate HEPA boxes for zoned pressure control, ensuring cross-contamination prevention between compounding and packaging areas.

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