Welcome to Farclean

Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms

Custom Dynamic Pass-Through Box Manufacturer for GMP Grade A Cleanrooms

GMP Grade A cleanroom environments demand precise surface sterilization measures before biological products, active pharmaceutical ingredients, or other sensitive goods enter manufacturing lines. As a specialized custom dynamic pass-through box manufacturer, Farclean designs and builds automated transfer enclosures engineered for complete microbial reduction and seamless integration with your cleanroom infrastructure including validated cleanroom doors and precision modular wall panels.

Innovative Transfer Chamber Design and Operation

Farclean dynamic pass-through boxes feature cutting-edge sterilization technology and versatile packaging solutions tailored to the most rigorous contamination control standards, ensuring your products maintain integrity throughout transfer:

  • Electrically Actuated Sliding Mechanism: Our patented piston-driven door system enables full hands-free operation, eliminating human intervention and potential cross-contamination for highly biosafety-sensitive facilities.
  • Modular Wall Panel Integration: Available as freestanding units or designed to interface seamlessly with cleanroom wall systems, allowing optimal configuration for product handling protocols.
  • Variable Cycle Sequencing: Customizable automation cycles precisely manage Dehumidification, Sterilization, Transfer, and Exhaust phases for zero or low bio-burden transfer between distinct cleanroom environments.
  • Advanced Catalytic Filtration: Integrated filter systems break down residual sterilizing agents, ensuring complete safety and environmental compliance in GMP settings.
  • Basketry Enclosure Options: Available with interchangeable, sterilized material holders designed for long-life with our durable wall panels.

Dynamic Pass-Through Box Performance Metrics

System Parameter Technical Specification GMP Compliance
Microbial Reduction 6-log kill reduction (Bacillus atrophaes spores) Conforms to ISO 14644-4 and EU GMP Annex 1 requirements.
Chamber Construction Type 304/316L SS with electropolished surfaces Full compatibility with ISO Class 1 to Class 7 environments.
Control Technology Fanuc servo automation with dual redundant PLC Validated operation meeting FDA 21 CFR Part 11 regulations.

Comprehensive Turnkey Integration

Boasting deep expertise in cleanroom systems, Farclean provides full engineering validation documentation, from Design Qualification to Performance Qualification, ensuring rapid regulatory approval and seamless integration with your existing cleanroom infrastructure. Interface with our specialized cleanroom doors engineers for optimum layout interlocking.

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