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

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

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

Technical Parameters:

SealAB Glue
Filtration GradeHepa Filter
NameCleanroom HEPA Filter
ApplicationCleanroom Termial Filteration System
MediaGlass Fibre Media
Other NameCleanroom Termial Filter
SpacerHot Melt Glue
FrameAluminum
Filter Efficiency99.995%@0.3um
GasketEVA /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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